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Chemical Class · Cannabinoids

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Item Number Product Sizes & Pricing CAS Purity Image Exclusive Introduction Date Mojo Plain Text Name Synonyms Keywords Interest
10009898 (−)-11-nor-9-carboxy-Δ9-THC-d3 (solution) 130381-15-6 ≥99% deuterated forms (d1-d3) 2010-11-12 8.249654696132 -11-nor-9-carboxy-9-thc-d3-solution THC metabolites Delta9-THC Δ9 THC tetrahydrocannabinols marijuana deuterateds deuterium internal standards mass spectrometry GC/MS LC/MS GC-MS LC-MS MS cannabinoids cbs synthetic 10916 8.249654696132
10009897 (−)-11-nor-9-carboxy-Δ9-THC (solution) 56354-06-4 ≥98% 2010-11-11 11.018646408839 -11-nor-9-carboxy-9-thc-solution THC metabolites Delta9-THC Δ9-THC tetrahydrocannabinols marijuana cannabinoids cbs synthetic 10915 11.018646408839
10010132 15-deoxy-Δ12,14-Prostaglandin J2-2-glycerol ester - ≥98% (isomer mixture) 2008-06-09 19.581055862492 15-deoxy-12-14-prostaglandin-j2-2-glycerol-ester 15-deoxy-Δ12,14-PGJ2-2-glycerol ester PPARgamma PPAR.gamma. PPARg PGD2 PGJ2 lipolysis prostaglandins adipocyte endocannabinoid metabolism diabetes obesity nuclear receptors COX-2 COX2 2-AG 2AG cannabinoids cbs synthetic 19.581055862492
14810 17-phenyl trinor Prostaglandin E2 38315-43-4 >98% 59.319171270718 17-phenyl-trinor-prostaglandin-e2 17-phenyl trinor PGE2 agonists EP1 EP3 prostaglandins receptors 17-phenyl-trinor-PGE2 59.319171270718
10004238 17-phenyl trinor Prostaglandin E2 serinol amide - ≥95% 2004-05-13 25.834298342541 17-phenyl-trinor-prostaglandin-e2-serinol-amide 17-phenyl trinor PGE2-SA agonists EP1 EP3 prostaglandins receptors 17-phenyl-trinor-PGE2 analogs 17-phenyl-PGE2SA 17-phenyl-PGE2-SA amides cannabinoids Cbs sythetic 25.834298342541
10004237 17-phenyl trinor Prostaglandin F2α serinol amide - ≥98% 2004-03-15 6.814792817679 17-phenyl-trinor-prostaglandin-f2-serinol-amide 17-phenyl trinor PGF2α-SA; Bimatoprost serinol amide analogs agonists receptors 17-phenyl-PGF2.alpha.SA 17-phenyl-PGF2alphaSA 17-phenyl-PGF2a-SA prostaglandins cannabinoids CBs synthetic 6.814792817679
362152 1-Arachidonoyl Glycerol-d5 - ≥99% deuterated forms (d1-d5) 36.490704419889 1-arachidonoyl-glycerol-d5 1-AG-d5 deuterium isotopes GC/MS endocannabinoids anandamides 1AG-d5 GC-MS mass spectrometry LC/MS LC-MS deuterated standards 1-AG-d5 internal fatty acids cannabinoids cbs synthetic 36.490704419889
11687 1'-Naphthoyl Indole New 109555-87-5 ≥98% 2012-05-01 100.035968650112 1-naphthoyl-indole indol-3-yl 1-naphthyl ketones synthetic cannabinoids CBs receptors CB1 central CB2 peripheral napthoylindole indoles herbals blends recreational cannabimimetics N-alkyl chains forensics designer drugs incense 100.035968650112
10008602 20-HETE Ethanolamide - ≥98% 2006-09-26 42.358876611418 20-hete-ethanolamide 20-hydroxy AEA; 20-hydroxy Arachidonoyl Ethanolamide hydroxy fatty acids omega-oxidation .omega.-oxidation w-oxidation cytochrome P450 CYP450 arachidonic HETEs metabolites P-450 vasoconstrictors vasoconstriction ethanolamides cannabinoids cbs synthetic 42.358876611418
10009962 2-(14,15-Epoxyeicosatrienoyl) Glycerol 848667-56-1 ≥95% 2008-04-03 39.494825046040 2-14-15-epoxyeicosatrienoyl-glycerol 2-14,15-EG 2-AG CYP450 metabolism mitogens cancers kidneys endocannabinoids cannabinoids cbs synthetic 39.494825046040
362162 2-Arachidonoyl Glycerol-d5 - ≥99% deuterated forms (d1-d5) 47.930980662983 2-arachidonoyl-glycerol-d5 2-AG-d5 deuterium isotopes GC/MS endocannabinoids anandamides 2AG-d5 GC-MS mass spectrometry LC/MS LC-MS deuterated standards 2-AG-d5 internal fatty acids lipids neurochemistry neuroscience endocrinology cannabinoids cbs synthetic 47.930980662983
362160 2-Arachidonoyl Glycerol-d8 - ≥99% deuterated forms (d1-d8) 84.020801104972 2-arachidonoyl-glycerol-d8 2-AG-d8 deuterium isotopes GC/MS endocannabinoids anandamides 2AG-d8 GC-MS mass spectrometry LC/MS LC-MS deuterated standards internal neurochemistry neuroscience endocrinology cannabinoids cbs synthetic 84.020801104972
10918 (±)3-epi CP 47,497-C8-homolog - ≥98% 2011-05-06 9.598423751790 -3-epi-cp-47-497-c8-homolog (±)-trans-CAY10596 (±)-3-epi CP 47,497-C8 analogs trans-CAY10596 cannabinoids analogs receptors by-product standards (+)-CP 47,497-C8 CB2 CP 47497 CP47497 CP-47497 CP-47,497 cbs synthetic 13802 9.598423751790
13802 (±)3-epi CP 47,497-C8-homolog (solution) Exclusive - ≥98% ✓ 2010-08-04 9.270452402875 -3-epi-cp-47-497-c8-homolog-solution (±)-trans-CAY10596 (±)-3-epi CP 47,497-C8 analogs trans-CAY10596 cannabinoids analogs receptors by-product standards (+)-CP 47,497-C8 CB2 CP 47497 CP47497 CP-47497 CP-47,497 cbs synthetic 10918 9.270452402875
13140 4-(n-nonyl) Benzeneboronic Acid 256383-45-6 ≥98% 2009-11-04 6.628153775322 4-n-nonyl-benzeneboronic-acid fatty acids amide hydrolase FAAH endocannabinoids arachidonoyl ethanolamides AEA inhibitors inhibit monoacylglycerol lipase MAGL 2-arachidonoyl glycerol 2-AG 2AG 2 AG inhibition cannabinoids cbs synthetic 6.628153775322
11093 4-Quinolone-3-Carboxamide CB2 Ligand New 1314230-69-7 ≥98% 2012-01-30 29.832711699173 4-quinolone-3-carboxamide-cb2-ligand 4Q3C CB2 Ligand CB1 CB2 cannabinoid CBs central peripheral receptors inverse agonists antinociception AM630 analgesic pain osteoporosis synthetic ligands mice analgesic AM 630 AM-630 29.832711699173
11094 4-Quinolone-3-Carboxamide Furan CB2 Agonist New 1314230-75-5 ≥98% 2012-02-28 32.235202229476 4-quinolone-3-carboxamide-furan-cb2-agonist 4Q3C CB2 Agonist cannabinoids CBs agonists receptors CB1 CB2 AM630 pain neuroscience osteoporosis inflammation anti-inflammatory bones research peripheral AM630 AM 630 AM-630 32.235202229476
13803 (±)5-epi CP 55,940 - ≥98% 2010-08-04 8.949804118533 -5-epi-cp-55-940 (±)-5-trans-CP 55,940 (±)-CP 55,940 cannabinoids analogs receptors pains analgesics by-products standards Δ9-THC delta-tetrahydrocannabidiol CP 55940 CP44950 CP-55940 CP55,940 8.949804118533
10005764 8-iso Prostaglandin F2α Ethanolamide - >98% 2004-09-24 34.617771639042 8-iso-prostaglandin-f2-ethanolamide 8-Isoprostane Ethanolamide; 8-epi PGF2α Ethanolamide; 8-iso PGF2α Ethanolamide; iPF2α-III Ethanolamide ethanolamides prostaglandins anandamides AEA COX-2 cox2 cyclooxygenases synthases isoprostanes 8-epi-PGF2alpha 8-iso-PGF2alpha arachidonoyl prostamides congeners decomposition standards non-enzymatic iPF2a-III PGHS2 PGHS-2 ethanolamines 714966-38-8 cannabinoids cbs sythetic 34.617771639042
11566 AKB48 Exclusive New 1345973-53-6 ≥98% ✓ 2012-04-30 346.902866392707 akb48 APINACA cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetics AKB 48 AKB-48 JWH018 JWH18 JWH 018 adamantyl carboxamide JWH-018 JWH 18 JWH-18 peripheral central 9001193 11564 STS-135 STS 135 STS135 346.902866392707
10005223 AM1172 251908-92-6 >98% 2004-09-01 24.112353433011 am1172 cannabinoids neurotransmitters inhibitors AEA lipids CB1 CB2 receptors anandamide hydrolysis fatty acids inhibits arachidonoyl ethanolamides reuptake FAAH-resistant amide hydrolases neuroscience neurochemistry cannabinoids cbs synthetic 24.112353433011
9001055 AM1220 137642-54-7 ≥98% 2011-10-11 95.776710483354 am1220 [1-[(1-methyl-2-piperidinyl)methyl]-1H-indol-3-yl]-1-naphthalenyl-methanone AM-2201 AM 2201 AM-1220 AM 1220 cannabinoids CB1 CB2 CBs receptors pains forensic science forensics 95.776710483354
11583 AM1220 azepane isomer Exclusive New - ≥98% ✓ 2012-05-15 154.933505217925 am1220-azepane-isomer cannabinoids CB1 herbals spices forensics cannabimimetics receptors agonists neurosciences CBs CB2 central peripheral AM-1220 AM 1220 isomers 154.933505217925
9001094 AM1235 Exclusive New 335161-27-8 ≥98% ✓ 2012-04-20 126.136499386126 am1235 cannabinoids CBs herbals incense receptors agonists CB1 CB2 forensics AM-1235 AM 1235 synthetic 126.136499386126
10010118 AM1241 444912-48-5 ≥97% 2007-08-29 98.893354337934 am1241 CB1 CB2 cannabinoids receptors agonists antagonists antinociception AM630 AM251 AM-1241 AM 1241 cannabinoids cbs synthetic AM1243 AM-1243 1243 98.893354337934
11282 AM1248 Exclusive New 335160-66-2 ≥98% ✓ 2012-02-06 65.101985322061 am1248 CBs cannabinoids synthetic agonist AM-1248 AMs 1248 forensic sciences receptors CB1 CB2 1-pentyl-3-(1-adamantoyl)indole AM679 AM-679 679 herbal blends smart products 65.101985322061
10707 AM2201 335161-24-5 ≥98% 2011-03-07 130.054011314727 am2201 cannabinoids CB1 CB2 receptors pain forensic sciences CBs AM-2201 AM 2201 130.054011314727
11194 AM2201 2-hydroxyindole metabolite Exclusive New - ≥98% ✓ 2012-05-15 102.711743400859 am2201-2-hydroxyindole-metabolite forensic sciences isomers cannabinoids CB1 CB2 urinary metabolites CBs central peripheral receptors AM-2201 AM 2201 102.711743400859
10862 AM2201 2'-naphthyl isomer Exclusive - ≥98% ✓ 2011-07-06 81.366833621524 am2201-2-naphthyl-isomer AM-2201 AM 2201 cannabinoids CBs isomers AMs forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetics 81.366833621524
11192 AM2201 6-hydroxyindole metabolite Exclusive New - ≥98% ✓ 2012-02-28 64.736433003919 am2201-6-hydroxyindole-metabolite cannabinoids CBs CB1 CB2 receptors pain forensic science neuroscience metabolites AM-2201 AM 2201 synthetic central peripheral P450 P-450 cytochromes blood urine 64.736433003919
11193 AM2201 7-hydroxyindole metabolite Exclusive New - ≥98% ✓ 2012-01-16 66.198490982941 am2201-7-hydroxyindole-metabolite forensics sciences AM-2201 AM 2201 isomers cannabinoids receptors pain CBs CB1 CB2 metabolites urinary urine metabolism synthetic central peripheral 66.198490982941
10706 AM2201-d5 Exclusive - ≥99% deuterated forms (d1- d5) ✓ 2011-05-16 53.678816923285 am2201-d5 cannabinoids CB1 CB2 receptors pain forensic sciences CBs AM2201 AM-2201 deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry standards 53.678816923285
9001031 AM2201 N-(2-fluoropentyl) isomer Exclusive New - ≥95% ✓ 2011-12-15 85.204461174323 am2201-n-2-fluoropentyl-isomer forensics AM-2201 AM 2201 isomers cannabinoids receptors pain CBs CB1 CB2 synthetic isomers fluorine pentyl chains synthetic central peripheral 85.204461174323
9001030 AM2201 N-(3-fluoropentyl) isomer Exclusive - ≥98% ✓ 2011-11-22 77.589468235752 am2201-n-3-fluoropentyl-isomer forensics AM-2201 AM 2201 isomers cannabinoids CBs receptors pain CBs CB1 CB2 77.589468235752
9001029 AM2201 N-(4-fluoropentyl) isomer Exclusive - ≥98% ✓ 2011-08-11 89.033418511995 am2201-n-4-fluoropentyl-isomer forensics sciences AM-2201 AM 2201 isomers cannabinoids receptors pain CBs CB1 CB2 central peripheral 89.033418511995
10203 AM2201 N-(4-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-10-11 122.314144531919 am2201-n-4-hydroxypentyl-metabolite AM-2201 AM 2201 cannabinoids cannabimimetic metabolites CB1 CB2 CBS receptors forensics synthetics smoking urinary urine potent synthetic 122.314144531919
11457 AM2201 N-(4-hydroxypentyl) metabolite-d5 Exclusive New - ≥99% deuterated forms (d1-d5) ✓ 2012-03-13 109.116260245029 am2201-n-4-hydroxypentyl-metabolite-d5 cannabinoids central peripheral metabolites CB1 CB2 receptors pain forensic sciences synthetics smoking urinary urine potent CBs AM2201 AM-2201 deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry standards 109.116260245029
11503 AM2232 New 335161-19-8 ≥95% 2012-03-29 93.166883692332 am2232 cannabinoids CBs CB1 CB2 central peripheral receptors forensics herbals incense agonists AM-2232 AM 2232 AMS 93.166883692332
11008 AM2233 444912-75-8 ≥98% 2011-10-24 109.136584896401 am2233 769958-75-0 forensic science cannabinoid receptors CB1 agonists WIN 55,212-2 WIN 55212-2 radioligands neuroscience 109.136584896401
11584 AM2233 azepane isomer Exclusive New - ≥98% ✓ 2012-05-08 163.905113566605 am2233-azepane-isomer cannabinoids CBs CB1 herbals spices forensics cannabimimetics agonists receptors neuroscience AM 2233 AM-2233 isomer 11008 163.905113566605
71670 AM251 183232-66-8 >98% 97.388179650992 am251 cannabinoids receptors antagonists CB1 analogs selective SR-141716-A AM-251 SR141716A neuroscience neurochemistry endocrinology 97.388179650992
13452 AM3102 Exclusive 213182-22-0 ≥98% ✓ 2009-08-11 40.003752932898 am3102 KDS-5104 OEA PPARs PPARα KDS5104 antiobesity anti-obesity CB1 CB2 endocannabinoids obesity cannabinoids inhibitors agonists receptors cbs synthetic 40.003752932898
90060 AM404 183718-77-6 >98% 33.186357081109 am404 N-(4-hydroxyphenyl)-Arachidonoyl Amide; 4-HPA cannabinoids neurotransmitter inhibitors AEA lipids CB1 CB2 receptors anandamide hydrolysis fatty acids neuroscience neurochemistry 33.186357081109
10006974 AM630 164178-33-0 ≥98% 2009-02-09 47.443079312365 am630 Iodopravadoline neurochemistry neuroscience cannabinoids CB1 CB2 antagonist inverse agonist antinociception pain receptors 47.443079312365
11504 AM679 Exclusive New 335160-91-3 ≥98% ✓ 2012-04-27 108.225876043367 am679 ams AM-679 AM 679 central peripheral receptors cannabinoids CBs CB1 CB2 incense agonists forensics spices designer drugs synthetic 108.225876043367
10567 AM694 Exclusive 335161-03-0 ≥95% ✓ 2011-01-31 60.006351580004 am694 cannabinoids CB1 CB2 receptors pain JWH neuroscience AM-694 AM 694 60.006351580004
10870 AM694 3-iodo isomer Exclusive - ≥98% ✓ 2011-08-31 54.127277000140 am694-3-iodo-isomer cannabinoids CBs cannabimimetic CB1 receptors agonists CB2 forensics sciences isomers AM 694 AM-694 synthetic analogs methanone indoles potent 3 iodo 54.127277000140
10869 AM694 4-iodo isomer Exclusive - ≥97% ✓ 2011-06-21 41.204834254143 am694-4-iodo-isomer cannabinoids CBs cannabimimetics CB1 CB2 pain spices forensics synthetic receptors agonists AM-694 AM 694 analogs neuroscience 41.204834254143
10008617 Arachidonic Acid Leelamide - ≥95% 2006-09-27 14.271160220994 arachidonic-acid-leelamide AA cannabinoids central peripheral CB1 CB2 CP55940 PDK pyruvates dehydrogenases kinases anti-inflammatory inflammation phospholipases PLA2 inhibits inhibitors inhibition cannabinoids cbs sythetic 14.271160220994
10007904 Arachidonoyl-1-thio-Glycerol Exclusive - ≥98% ✓ 2006-01-24 17.398674033149 arachidonoyl-1-thio-glycerol 1-S-Arachidonoyl-1-mercapto-2,3-propanediol cannabinoids monoacylglycerols monoglycerol monoglyceride anandamides fatty acids neurochemistry neuroscience chromogenic substrates lipases 2-arachidonoyls 2-AG agonists central CB1 nervous system CNS rat brains MGL hydrolyzes arachidonic acids thioesters analogs thiols DTNB Ellman's reagents yellow cannabinoids cbs synthetic 17.398674033149
10011178 Arachidonoyl Ethanolamide-d4 946524-40-9 ≥99% deuterated forms (d1-d4) 2008-03-04 40.586823204420 arachidonoyl-ethanolamide-d4 AEA-d4; Anandamide-d4 deuterium GC/MS internal isotopes standards ethanolamides LC/MS mass spectrometry cannabinoids fatty acids deuterated neurochemistry neuroscience ethanolamines cannabinoids cbs synthetic 40.586823204420
10180 Arachidonoyl Ethanolamide Phosphate 183323-26-4 >98% 2004-08-19 21.402127071823 arachidonoyl-ethanolamide-phosphate AEA-P; Anandamide Phosphate endocannabinoids neurotransmitters ligands lipids CB1 CB2 receptors fatty acids phosphates anandamides LPA lysophosphatidic ethanolamines ethanolamides cannabinoids cbs synthetic 21.402127071823
62170 Arachidonoyl Serinol 183718-70-9 >98% 37.453093922652 arachidonoyl-serinol endocannabinoids anandamides 2AG CB1 receptors neurochemistry neuroscience cannabinoids cbs synthetic 37.453093922652
13823 AX 048 Exclusive 873079-69-7 ≥98% ✓ 2010-09-15 7.192651933702 ax-048 Inflammation antihyperalgesia cPLA2 phospholipases inhibitors inhibition inhibits AX048 AX-048 signaling signalling group IVA PLA2 cannabinoids cbs synthetic Acids Octanoic Octanoic Acids 7.192651933702
10506 Bio-active Lipid I Screening Library (96-Well) - 2010-06-15 39.676215469613 bio-active-lipid-i-screening-library-96-well vasoconstriction bronchoconstriction prostaglandins endocrinology prostaglandins HTS high thoroughput screening cannabinoids cbs synthetic 39.676215469613
90080 Cannabidiol 13956-29-1 >99% 31.817340173638 cannabidiol CBD delta9-THC .DELTA.9-THC delta9THC .DELTA.9THC marijuana neuroprotective tetrahydrocannabidiol d9-THC d9THC neurochemistry neuroscience synthetic cbs cannabinoids 31.817340173638
13285 Cannabidiol dimethyl ether 1242-67-7 ≥98% 2009-05-19 8.183425414364 cannabidiol-dimethyl-ether Cannabidiol-2',6'-dimethyl ether; CBDD 15-lipoxygenases 15-LOs dioxygenase fatty acids inflammation thrombosis cancer LDL oxidation inhibitions inhibition inhibiting cannabinoids cbs synthetic 8.183425414364
90081 Cannabidiol (solution) 13956-29-1 ≥99% 2011-03-03 45.111998995479 cannabidiol-solution CBD delta9-THC .DELTA.9-THC delta9THC .DELTA.9THC marijuana neuroprotective tetrahydrocannabidiol d9-THC d9THC neurochemistry neuroscience synthetic cbs cannabinoids 45.111998995479
10508 Cannabinoid Agonist Screening Library (96-Well) - 2011-05-05 16.574585635359 cannabinoid-agonist-screening-library-96-well plates screening cannabinoids CBs libraries foresnics JWHs JWH-108 JWH-200 HU 210 CPs 16.574585635359
71652 CAY10401 288862-89-5 >98% 2005-02-02 7.964372007366 cay10401 FAAH inhibitors analgesics fatty acids amides hydrolases inhibits inhibition hydrolysis hydrolyze CAY-10401 inactivation anandamides AEA arachidonoyl ethanolamides neuroscience neurochemistry cannabinoids cbs synthetic 7.964372007366
10009523 CAY10429-d3 - ≥99% deuterated forms (d1-d3) 2007-10-02 4.785082872929 cay10429-d3 Abnormal Cannabidiol-d3; Abn-CBD-d3 endocannabinoids cannabidiols abnormal abn-cbd non-CB1 non-CB2 receptors agonists BV-2 microglials hypotensives GPCR neurochemistry neurosciences cannabindoids CB1 CB2 deuterated deuterium mass spectrometry LC-MS GC-MS AbnCBD LC/MS GC/MS cannabinoids cbs synthetic 4.785082872929
10008669 CAY10508 878533-35-8 ≥98% 2006-08-04 35.284060773480 cay10508 1,3-bis(4-bromophenyl)-5-phenyl-Imidazolidine-2,4-dione central peripheral cannabinoids receptors inverse agonists antagonists therapeutic therapy obesity drug dependence CB1 CB2 CP-55,940 cannabinoids cbs synthetic 35.284060773480
10010398 CB-13 432047-72-8 ≥98% 2009-06-30 38.500490737732 cb-13 CRA-13 cannabinoids CB1 CB2 central peripheral receptors agonists pains hyperalgesia blocks blocking CB13 CB 13 CRA13 CRA 13 38.500490737732
10006590 CB1 Receptor (C-Term) Polyclonal Antibody - 2005-05-10 74.772228360957 cb1-receptor-c-term-polyclonal-antibody Cannabinoid Receptor 1 cannabis .DELTA.9-tetrahydrocannabinol anandamides D9-THC antibodies receptors DELTA9-tetrahydrocannabinol D9-tetrahydrocannabinol .DELTA.9-THC DELTA9-THC western blots blotting antisera antiserum WB IHC immunohistochemistry neuroscience neurochemistry endocrinology immunoblotting cannabinoids cbs synthetic 74.772228360957
10010116 CB-25 Exclusive 869376-63-6 >98% ✓ 2007-10-25 20.448853591160 cb-25 cannabinoids ligands receptors CB1 CB2 THC anandamides AEA inverse agonists cannabinoids cbs synthetic 20.448853591160
10010117 CB-52 Exclusive 869376-90-9 ≥98% ✓ 2007-10-25 20.362948895028 cb-52 cannabinoids ligands receptors CB1 CB2 THCs anandamides AEAs partial agonists neutral antagonists cannabinoids cbs synthetic 20.362948895028
13289 CB-86 Exclusive 1150586-64-3 ≥98% ✓ 2010-05-03 23.170741910023 cb-86 cannabinoids receptors CB1 CB2 antinociception agonists resorcinol anandamides hybrids CB86 CB 86 partial agonist neural antagonist antinociceptive effects 2-beta-D-Ribofuranosyl-1,2,4-triazine-3,5(2H,4H)-dione 6-Azauridine 6 Azauridine Azauridine cannabinoids cbs synthetic 23.170741910023
10917 (−)-CP 47, 497 114753-51-4 ≥98% 2011-05-05 12.763946616612 -cp-47-497 cannabinoids analgesia CB1 hypothermia motor deppressant anticonvulsant Δ9-THC analogs activity hypothermic effects cannabinoids cbs synthetic 13218 12.763946616612
10910 (+)-CP 47,497 134308-14-8 ≥98% 2011-05-05 13.281073688435 -cp-47-497 cannabinoid analgesia analgesic CB1 hypothermia motor depressant anticonvulsant Δ9-THC CBs analogs cbs synthetic cannabinoids 13.281073688435
10913 (±)-CP 47,497 70434-82-1 ≥98% 2011-05-05 34.382032339974 -cp-47-497 receptors agonist CB1 potent cannabinoid DELTA9-THC Δ9-THC CP47,497 CP-47,497 CP47497 CP-47497 cannabinoids cbs synthetic 16851 34.382032339974
9000774 (±)-CP 47,497-C7-hydroxy metabolite - ≥95% 2011-11-04 66.972189993861 -cp-47-497-c7-hydroxy-metabolite cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic metabolites herbal adulterant CP47,497 CP-47,497 66.972189993861
10908 (±)-CP 47,497-C8-homolog Exclusive 70434-92-3 ≥98% ✓ 2011-05-06 33.614779595787 -cp-47-497-c8-homolog CAY10596; Cannabicyclohexanol cannabinoids analgesia analgesic CB1 hypothermia motor supressants anticonvulsant Δ9-THC C8 analog CP 47,497-C8 CP4 ,497-C8 cannabinoids cbs synthetic 33.614779595787
9000773 CP 47,497-C8-homolog C-8-hydroxy metabolite New - ≥98% 2012-01-03 24.703571209330 cp-47-497-c8-homolog-c-8-hydroxy-metabolite cannabinoids cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic CP-47497 CP 47,497 47,497 CPs CP47497 CP47,497 herbal blends CBs monophenols adulterant metabolites 24.703571209330
10686 (±)-CP 47,497-C8-homolog-d7 (solution) Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-03-14 25.726973152059 -cp-47-497-c8-homolog-d7-solution Cannabicyclohexanol-d7 cannabinoids analgesia analgesic CB1 hypothermia motor supressants anticonvulsant Δ9-THC C8 analog CP 47,497-C8 CP4 ,497-C8 cannabinoids cbs synthetic deuterateds deuteriums LC-MS LC/MS GC-MS GC/MS mass spectrometry MS GC LC standards stds 10914 25.726973152059
13216 (±)-CP 47,497-C8-homolog (solution) Exclusive 70434-92-3 ≥98% ✓ 2009-04-23 43.928671821398 -cp-47-497-c8-homolog-solution CAY10596; Cannabicyclohexanol cannabinoids analgesia analgesic CB1 hypothermia motor supressants anticonvulsant Δ9-THC C8 analog CP 47,497-C8 CP4 ,497-C8 cannabinoids cbs synthetic 10908 43.928671821398
10687 (±)-CP 47,497-d11 (solution) Exclusive - ≥99% deuterated forms (d1-d11) ✓ 2011-02-16 34.319074410242 -cp-47-497-d11-solution receptors agonist CB1 potent cannabinoid DELTA9-THC Δ9-THC CP47,497 CP-47,497 CP47497 CP-47497 cannabinoids cbs synthetic deuterated deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS 10907 34.319074410242
10889 CP 47,497-para-quinone analog Exclusive - ≥90% ✓ 2011-07-13 12.459427767546 cp-47-497-para-quinone-analog CP47,497 CP-47,497 analogs cannabinoids CBs forensics sciences quinones paraquinone CP47497 CP-47497 47497 47,497 cannabimimetics CB1 CB2 receptors agonists spices synthetics 12.459427767546
13218 (−)-CP 47,497 (solution) 114753-51-4 ≥98% 2009-04-13 17.412952685231 -cp-47-497-solution cannabinoids analgesia CB1 hypothermia motor deppressant anticonvulsant Δ9-THC analogs activity hypothermic effects cannabinoids cbs synthetic 10917 17.412952685231
13219 (+)-CP 47,497 (solution) 134308-14-8 ≥98% 2009-04-13 18.224339434425 -cp-47-497-solution cannabinoid analgesia analgesic CB1 hypothermia motor depressant anticonvulsant Δ9-THC CBs analogs cbs synthetic cannabinoids 10910 18.224339434425
16851 (±)-CP 47,497 (solution) 70434-82-1 ≥98% 2008-12-10 49.485946899938 -cp-47-497-solution receptors agonist CB1 potent cannabinoid DELTA9-THC Δ9-THC CP47,497 CP-47,497 CP47497 CP-47497 cannabinoids cbs synthetic 10913 49.485946899938
90084 (−)-CP 55,940 83002-04-4 ≥98% 2007-01-15 42.173747156320 -cp-55-940 CP 55940 CP-55940 CP-55,940 agonists cannabinoids CB1 CB2 THC receptors endocrinology cp55940 cp55,940 neurochemistry cbs synthetic 42.173747156320
13608 (+)-CP 55,940 Exclusive - ≥98% ✓ 2010-05-20 22.036376965575 -cp-55-940 Δ9-THC cannabinoids CB1 CB2 pain analgesic cannabinoids cbs synthetic 22.036376965575
13241 (±)-CP 55,940 Exclusive 83003-12-7 ≥98% ✓ 2009-05-20 21.967687152834 -cp-55-940 cannabinoids analgetic pain THC thermal mechanical chemicals receptors CB1 cannabimimetic potent non-selective CP55940 CP-55940 cbs synthetic 21.967687152834
10007534 Docosahexaenoyl Ethanolamide Exclusive 162758-94-3 ≥98% ✓ 2006-02-17 20.422555781719 docosahexaenoyl-ethanolamide DHEA; DEA neurochemistry neuroscience endocannabinoids brain retina docosahexaenoic acids DHA fatty w-3 .omega.-3 neural tissues ethanolamines ethanolamides arachidonoyl AEA lipids extracts piglets diets rats CB1 receptors shaker-related voltage-gated potassium channels cannabinoids cbs synthetic DEA 20.422555781719
9001108 Docosahexaenoyl Ethanolamide-d4 Exclusive New 946524-43-2 ≥99% deuterated forms (d1-d4) ✓ 2012-02-21 19.810945429872 docosahexaenoyl-ethanolamide-d4 DHEA-d4; DEA-d4 neurochemistry neuroscience endocannabinoids brain retina docosahexaenoic acids DHA fatty w-3 .omega.-3 neural tissues ethanolamines ethanolamides arachidonoyl AEA lipids extracts piglets diets rats CB1 receptors shaker-related voltage-gated potassium channels cannabinoids cbs synthetic DEA deuterateds deuteriums LC-MS GC/MS GC-MS mass spectrometry LC/MS MS 19.810945429872
10964 Eicosapentaenoyl Ethanolamide 109001-03-8 ≥98% 2011-06-22 57.375516969219 eicosapentaenoyl-ethanolamide EPEA cannabinoids CBSs endocannabinoids forensic sciences signals signaling N-acylethanolamide N-acylethanolamine NAE dietary restrictions lifespans TOR nematodes eicosapentaenoic acids inflammation anti-inflammatory 57.375516969219
10919 (±)-epi CP 47, 497 - ≥98% 2011-05-05 9.598423751790 -epi-cp-47-497 3-trans CP 47,497 (±)-trans-CP 47,497 cannabinoids analogs receptors CB1 standards (±)-CP47,497 analgesic potency epimer THC .delta.-THC (±)-iso Δ-tetrahydrocannabidiol CP 47497 CP47497 CP-47497 CP-47,497 cbs synthetic 13801 9.598423751790
13801 (±)-epi CP 47,497 (solution) Exclusive - ≥98% ✓ 2010-08-04 9.334116612362 -epi-cp-47-497-solution 3-trans CP 47,497 (±)-trans-CP 47,497 cannabinoids analogs receptors CB1 standards (±)-CP47,497 analgesic potency epimer THC .delta.-THC (±)-iso Δ-tetrahydrocannabidiol CP 47497 CP47497 CP-47497 CP-47,497 cbs synthetic 10919 9.334116612362
10004236 Fluprostenol serinol amide - ≥98% 2004-09-23 7.056596685083 fluprostenol-serinol-amide Flu-SA PGF2.alpha. PGF2alpha analogs agonists prostaglandins receptors amides cannabinoids CB1 CBs synthetic 7.056596685083
10011357 Glycerophospho-N-Oleoyl Ethanolamine Exclusive 201738-24-1 ≥98% ✓ 2009-02-20 24.612817679558 glycerophospho-n-oleoyl-ethanolamine cannabinoids neurotransmitter PPARs neurochemistry neuroscience fatty acids amides hydrolase oleoyl ethanolamides methabolism obesity nutrition diet NAPE N-Acyl Phosphatidylethanolamide cannabinoids cbs synthetic 24.612817679558
10011356 Glycerophospho-N-Palmitoyl Ethanolamine Exclusive 100575-09-5 ≥98% ✓ 2009-03-12 7.585174953959 glycerophospho-n-palmitoyl-ethanolamine GP-NPEA; GP-NAE cannabinoids neurotransmitter neurochemistry neuroscience fatty acids amides hydrolase FAAHs palmitoyl ethanolamides inflammation anti-inflammatory C16:0 CBS NAPE N-Acyl Phosphatidylethanolamide cannabinoids cbs synthetic 7.585174953959
10224 GPR55 Polyclonal Antibody - 2010-01-19 42.302316495658 gpr55-polyclonal-antibody G Protein-Coupled Receptor 55 proteins receptors antibodies western blots WB ICC signals signaling nucleotides THC amino acids blotting immunoblotting immunocytochemistry signalling cannabinoids cbs synthetic 42.302316495658
10010372 GW 842166X 666260-75-9 ≥98% 2008-05-23 34.145428176795 gw-842166x inflammatory pain arthritis neuropathic hyperalgesia CB2 cannabinoids agonists anandamide receptors neurochemistry cannabinoids cbs synthetic 34.145428176795
10011038 Hemopressin - 2009-08-13 29.761006314127 hemopressin peptides antagonist inhibitors inhibits inhibition hypertension binding asoactive vasoactive cannabinoids cbs synthetic 29.761006314127
10006371 Hormone Sensitive Lipase Polyclonal Antibody - 2005-06-22 9.506293738489 hormone-sensitive-lipase-polyclonal-antibody HSL; LIPE proteins antibodies antisera antiserum WB western blots blotting IHC immunohistochemistry ICC immunocytochemistry catalyses hydrolysis of tri- di- monoacylglycerols cholesterol esters mobilizes fatty acids primary source energy mammals enzyme expressed adipose tissues stearidonic steroidgenesis spermatogenesis foam cell formation atherosclerosis diabetic pathology human cDNA isoforms testis mRNA mouse murine macrophages testicular ram seminal vesicles triacylglycerols diacylglycerols atherosclerosis 9.506293738489
90082 HU-210 112830-95-2 >98% 45.112620856353 hu-210 agonists analogs d9-THC marijuana CB1 CB2 receptors cannabinoids HU210 .DELTA.9-THC delta9-THC neuroscience neurochemistry endocrinology cannabinoids cbs synthetic 45.112620856353
90083 HU-210 (solution) 112830-95-2 ≥98% 2011-03-03 30.987411207576 hu-210-solution agonists analogs d9-THC marijuana CB1 CB2 receptors cannabinoids HU210 .DELTA.9-THC delta9-THC neuroscience neurochemistry endocrinology cannabinoids cbs synthetic Tetrahydrocannabinol, Trans-(+-)-Isomer Tetrahydrocannabinol, (6a-trans)-Isomer Tetrahydrocannabinol (6aS-cis)-Isomer Tetrahydrocannabinol (6aR-cis)-Isomer Solvay Brand of Tetrahydrocannabinol Tetrahydrocannabinol Trans-Isomer Tetrahydrocannabinol Trans Isomer delta(9)-Tetrahydrocannabinol delta(1)-Tetrahydrocannabinol 9-ene-Tetrahydrocannabinol 9 ene Tetrahydrocannabinol Tetrahydrocannabinol delta(9)-THC delta(1)-THC Dronabinol Marinol THC 30.987411207576
10005673 HU-331 137252-25-6 ≥95% 2005-09-09 39.848813177818 hu-331 cannabidiols analogs antiproliferative activity endocannabinoids central CB1 peripheral CB2 non-CB receptor-mediated pharmacology receptors memory weight loss appetite neurodegeneration tumor surveillance analgesia inflammation hydroxylquinone antineoplastic human cancer cells lines inhibits inhibitors inhibition growth Raji Jurkat lymphomas in vitro HT-29 colon carcinomas neuroscience neurochemistry cannabinoids cbs sythetic 39.848813177818
70275 IMMA - ≥98% 12.406973603437 imma Indomethacin Morpholinylamide; BML-190 cannabinoids receptors CB2 neuroscience neurochemistry endocrinology 12.406973603437
10008661 JP104 Exclusive - ≥98% ✓ 2006-09-05 7.391034655951 jp104 click chemistry probes FAAH fatty acids amides hydrolases inhibits inhibitors inhibition URB598 acyl anandamide AEA esters unsaturated carbamates neurochemistry 7.391034655951
10266 JWH 007 Exclusive 155471-10-6 ≥98% ✓ 2011-02-23 32.475658424607 jwh-007 agonists cannabinoids receptors CB1 CB2 Δ9-THC pain antinociception hypothermia catalepsy JWHs CBs JWH-007 JWH007 JWH-7 JWH 7 JWH7 32.475658424607
10486 JWH 007-d9 - ≥99% deuterated forms (d1-d9) 2010-10-11 38.180851749539 jwh-007-d9 agonists cannabinoids receptors CB1 CB2 Δ9-THC pain antinociception hypothermia catalepsy deuterateds deuteriums mass spectrometry MS standards JWHs JWH007-d9 JWH-007-d9 cannabinoids cbs synthetic JWH7-d9 JWH 7-d9 JWH-7-d9 38.180851749539
9001058 JWH 011 Exclusive 155471-13-9 ≥98% ✓ 2011-09-06 22.113556607671 jwh-011 JWH 004 1-methylhexyl analog JWH011 JWH-011 JWH11 JWH-11 JWH015 JWH-015 JWH15 JWH-15 JWHs analogs forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics central peripheral 22.113556607671
10009018 JWH 015 155471-08-2 ≥98% 2006-10-05 63.861233412638 jwh-015 agonists CB1 CB2 cannabinoids aminoalkylindole receptors MS multiple sclerosis WIN 55212-2 ACEA CD4+ T cells IFN-g IFN-.gamma. CD40 JAK STAT1 endocrinology neurochemistry JWH015 JWH-015 cannabinoids cbs synthetic JWH15 JWH-15 JWH 15 63.861233412638
10660 JWH 015-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-02-21 44.219281767956 jwh-015-d7 agonists CB1 CB2 cannabinoids aminoalkylindole receptors MS multiple sclerosis WIN 55212-2 ACEA CD4+ T cells IFN-γ IFN-gamma CD40 JAK STAT1 endocrinology neurochemistry JWH015 JWH-015 cannabinoids cbs synthetic LC-MS LC/MS GC-MS GC/MS mass spectrometry deuteriums deuterateds standards JWH15-d7 JWH 15-d7 JWH-15-d7 44.219281767956
10849 JWH 016 Exclusive 155471-09-3 ≥95% ✓ 2011-07-13 39.249040409395 jwh-016 JWH016 JWH-016 cannabinoids CBs receptors isomers forensics sciences JWHs agonists cannabimimetics CB1 CB2 receptors agonists spices synthetics 39.249040409395
10900 JWH 018 209414-07-3 ≥98% 2011-05-05 28.369097520404 jwh-018 cannabinoids CB1 CB2 agonists selective receptors WIN 55212-2 JWH-018 JWH018 cbs synthetic JWH 18 JWH-018 JWH18 JWH-18 13169 28.369097520404
9000844 JWH 018 2-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-10-26 19.190639893467 jwh-018-2-hydroxyindole-metabolite cannabinoids receptors WIN 55212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics CBs monohydroxylated cbs synthetic JWH-018 JWH018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 19.190639893467
10711 JWH 018 2-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-02-25 12.710481456396 jwh-018-2-hydroxyindole-metabolite-d9 cannabinoids CB1 CB2 agonists selective receptors WIN 55,212-2 JWH-018 JWH018 deuterateds deuteriums CBs cannabinoids LC-MS LC/MS GC-MS GC/MS mass spectrometry MS synthetic cannabimimetics urine urinary metabolites glucuroconjugate forensics CBs monohydroxylated standards JWH-018 JWH018 JWH18 JWH-18 JWH 18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 12.710481456396
9001004 JWH 018 2'-naphthyl isomer Exclusive 1131605-25-8 ≥98% ✓ 2011-06-20 29.137832547709 jwh-018-2-naphthyl-isomer JWH018 JWH-018 CBs cannabinoids forensics sciences cannabimimetic CB1 CB2 receptors agonist spices synthetic 29.137832547709
9001006 JWH 018 2'-naphthyl-N-(1,2-dimethylpropyl) isomer Exclusive - ≥98% ✓ 2011-10-11 9.060741372904 jwh-018-2-naphthyl-n-1-2-dimethylpropyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic herbal blends isomers JWH-018 JWH018 JWH18 JWH-18 18 9.060741372904
11586 JWH 018 2’-naphthyl-N-(1-ethylpropyl) isomer Exclusive New - ≥98% ✓ 2012-04-03 60.270715257992 jwh-018-2-naphthyl-n-1-ethylpropyl-isomer neuroscience synthetic cannabinoids CBs herbals blends isomers forensics cannabimimetics CB1 CB2 receptors agonists central peripheral spices 60.270715257992
9001009 JWH 018 2'-naphthyl-N-(1-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-20 18.298877751904 jwh-018-2-naphthyl-n-1-methylbutyl-isomer JWH018 JWH-018 CBs cannabinoids forensics sciences cannabimimetic CB1 CB2 receptor agonist spices synthetic 18.298877751904
9001008 JWH 018 2'-naphthyl-N-(2,2-dimethylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-28 13.821061205240 jwh-018-2-naphthyl-n-2-2-dimethylpropyl-isomer JWH-018 JWH018 JWH-18 JWH18 JWH 18 cannabinoids CBs forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetics 13.821061205240
9001010 JWH 018 2'-naphthyl-N-(2-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-13 12.288551387083 jwh-018-2-naphthyl-n-2-methylbutyl-isomer JWH-018 JWH018 JWH 18 JWH18 JWH-18 forensics cbs cannabinoids isomers cannabimimetic CB1 CB2 receptors agoinsts spices synthetic pentyl chains herbal blends 12.288551387083
9001005 JWH 018 2'-naphthyl-N-(3-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-13 10.940436470858 jwh-018-2-naphthyl-n-3-methylbutyl-isomer JWHs isomers forensic science cannabinoids CBs JWH-018 JWH018 JWH18 JWH-18 CB1 CB2 receptors agonist spices synthetic 10.940436470858
9000851 JWH 018 4-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 29.965426746809 jwh-018-4-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolites 1 glucuroconjugate forensics JWH-018 JWH018 209414-07-3 JWH018-metabolite JWH 018-metabolite one CBs M-1 M1 smoking mixtures spices cbs synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 29.965426746809
10712 JWH 018 4-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-02-25 15.974211548210 jwh-018-4-hydroxyindole-metabolite-d9 cannabinoids CB1 CB2 agonists selective receptors WIN 55,212-2 JWH-018 JWH018 deuterateds deuteriums CBs cannabinoids LC-MS LC/MS GC-MS GC/MS mass spectrometry MS synthetic cannabimimetics urine urinary metabolites 1 glucuroconjugate forensics smoking mixtures spices standards JWH-018 JWH018 JWH18 JWH-18 JWH 18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 15.974211548210
9000852 JWH 018 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 31.649293691525 jwh-018-5-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 foresnsic science pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite two 2 smoking mixtures spices CBS M-2 M2 synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 31.649293691525
10713 JWH 018 5-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-03-11 16.057740414512 jwh-018-5-hydroxyindole-metabolite-d9 cannabinoids CB1 CB2 agonists selective receptors WIN 55,212-2 JWH-018 JWH018 deuterateds deuteriums CBs cannabinoids LC-MS LC/MS GC-MS GC/MS mass spectrometry MS synthetic cannabimimetics urine urinary metabolites 1 glucuroconjugate forensics smoking mixtures spices standards M-2 M2 JWH-018 JWH018 JWH18 JWH-18 JWH 18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 16.057740414512
9000853 JWH 018 6-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 30.292668565763 jwh-018-6-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics JWH-018 JWH018 209414-07-3 science pain neuroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite three 3 M-3 M3 CBs smoking mixture spices cbs synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 30.292668565763
10714 JWH 018 6-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-03-25 29.737593084863 jwh-018-6-hydroxyindole-metabolite-d9 cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugates forensics JWH-018 JWH018 209414-07-3 science pain neuroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite three 3 M-3 M3 CBs smoking mixture spices cbs synthetic deuterateds deuteriums LC-MS LC/MS GC-MS GC/MS mass spectrometry MS standards JWH-018 JWH018 JWH18 JWH-18 JWH 18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 29.737593084863
10697 JWH 018 6-methoxyindole analog Exclusive - ≥98% ✓ 2011-02-15 19.075558118861 jwh-018-6-methoxyindole-analog analogs metabolites cannabinoids receptors agonists CBs JWH-018 JWH018 JWH18 JWH-18 JWH 18 19.075558118861
9000854 JWH 018 7-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 26.744422027828 jwh-018-7-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 foresnsic science pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite four 4 M4 M-4 smoking mixtures spices synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 26.744422027828
10715 JWH 018 7-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-07-26 8.456755434286 jwh-018-7-hydroxyindole-metabolite-d9 WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugates forensics JWH-018 JWH018 209414-07-3 science pain neuroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite three 3 M-3 M3 smoking mixture spices synthetic deuterateds deuteriums LC-MS LC/MS GC-MS GC/MS mass spectrometry MS standards cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 CBs cannabimimetics urine urinary metabolites glucuroconjugate forensics JWH-018 JWH018 209414-07-3 foresnsic sciences pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite 4 M4 M-4 smoking mixtures spices synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 8.456755434286
9000799 JWH 018 adamantyl analog Exclusive - ≥97% ✓ 2011-07-18 42.958777573540 jwh-018-adamantyl-analog AB-001 JWH 018 JWH-018 JWHs analogs forensics sciences cannabinoids CBs receptors WIN 55,212-2 CB1 CB2 cannabimimetics 42.958777573540
9001193 JWH 018 adamantyl carboxamide Exclusive New 1345973-50-3 ≥98% ✓ 2012-03-08 139.322541233127 jwh-018-adamantyl-carboxamide 2NE1; APICA JWHs JWH018 JWH-018 JWH18 JWH 18 JWH-18 cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics science neuroscience synthetic central peripheral herbal blends analogs 139.322541233127
13824 JWH 018-d9 (solution) - ≥99% deuterated forms (d1-d9) 2010-06-21 48.264956879881 jwh-018-d9-solution cannabinoids CB1 CB2 agonists selective receptors WIN 55,212-2 JWH-018 JWH018 deuterateds deuteriums CBs cannabinoids LC-MS LC/MS GC-MS GC/MS mass spectrometry MS cbs synthetic JWH018-d9 JWH-018-d9 JWH-18-d9 JWH 18-d9 JWH18-d9 JWH18d9 10901 48.264956879881
9001000 JWH 018 N-(1,1-dimethylpropyl) isomer Exclusive - ≥98% ✓ 2011-11-16 8.808625499578 jwh-018-n-1-1-dimethylpropyl-isomer cannabinoids cannabimimetics CBs CB1 CB2 receptors agonists spices forensics synthetic JWHs JWH018 JWH-018 JWH18 JWH 18 JWH-18 isomers herbal central peripheralpentyl chains 8.808625499578
9001003 JWH 018 N-(1,2-dimethylpropyl) isomer Exclusive - ≥98% ✓ 2011-10-11 10.446707583240 jwh-018-n-1-2-dimethylpropyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic herbal blends isomers JWH-018 JWH018 JWH18 JWH-18 18 10.446707583240
11585 JWH 018 N-(1-ethylpropyl) isomer Exclusive New - ≥98% ✓ 2012-04-03 81.793275619358 jwh-018-n-1-ethylpropyl-isomer neuroscience synthetic cannabinoids CBs herbals blends isomers forensics cannabimimetics CB1 CB2 receptors agonists central peripheral spices 81.793275619358
9001002 JWH 018 N-(1-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-17 13.607471345279 jwh-018-n-1-methylbutyl-isomer JWH 073 1-methylbutyl homolog JWH-018 JWH018 CBs cannasbinoids forensic sciences cannabimimetic CB1 CB2 receptors agonist spices synthetic 13.607471345279
9001001 JWH 018 N-(2,2-dimethylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-27 16.964924358661 jwh-018-n-2-2-dimethylpropyl-isomer JWH018 JWH-018 JWH18 JWH-18 JWH 18 cannabinoids CBs forensics sciences cannabimimetics CB1 CB2 receptors agonists spices forensic synthetics 16.964924358661
11119 (±)-JWH 018 N-(2-hydroxypentyl) metabolite New - ≥98% 2011-12-07 27.955279721688 -jwh-018-n-2-hydroxypentyl-metabolite cannabinoids metabolites incense forensics urine urinary herbals JWHs JWH018 JWH-018 JWH 18 JWH18 JWH-18 serum alkyl cytochromes P450 CBs potent synthetic herbal blends CYP450 CYP-450 serum urine 27.955279721688
10690 JWH 018 N-(2-methylbutyl) isomer Exclusive - ≥97% ✓ 2011-03-16 18.135527365523 jwh-018-n-2-methylbutyl-isomer JWH 073 2-methylbutyl homolog cannabinoids CBs receptors WIN 55,212-2 CB1 cannabimimetics analogs forensics standards JWH-073 JWH 73 JWH73 JWH-73 18.135527365523
11118 (±)-JWH 018 N-(3-hydroxypentyl) metabolite - ≥98% 2011-11-17 24.623797326563 -jwh-018-n-3-hydroxypentyl-metabolite cannabinoids metabolites incense forensics urine urinary herbal CBs JWHs JWH018 JWH-018 JWH 18 JWH18 JWH-18 monohydroxylation alkyl chainscytochromes P450 serum 24.623797326563
10691 JWH 018 N-(3-methylbutyl) isomer - ≥97% 2011-02-07 18.534992637709 jwh-018-n-3-methylbutyl-isomer JWH 073 3-methylbutyl homolog cannabinoids agonist selective receptors WIN55212-2 WIN552122 WIN 55212-2 WIN 55,212-2 CB1 cannabimimetics analog forensics CBs JWH-073 JWH-73 JWH 73 JWH73 18.534992637709
11075 JWH 018 N-(4,5-epoxypentyl) analog - ≥98% 2011-10-21 22.906958377970 jwh-018-n-4-5-epoxypentyl-analog JWH 018 epoxide cannabinoids CBs cannabimimetic CB1 CB2 receptor agonists spices forensics synthetic herbal central peripheral alkyl chains 22.906958377970
10921 (−)-JWH 018 N-(4-hydroxypentyl) metabolite New - ≥98% 2011-12-07 23.904092435465 -jwh-018-n-4-hydroxypentyl-metabolite cannabinoids CBs metabolites incense forensics urine urinary herbal blends JWHs JWH018 JWH-018 JWH 18 JWH-18 JWH18 enantiomers potent synthetic phase 1 phase I phase one glucuronidated enantiomer 23.904092435465
10920 (+)-JWH 018 N-(4-hydroxypentyl) metabolite New - ≥98% 2011-12-07 32.497115079313 -jwh-018-n-4-hydroxypentyl-metabolite cannabinoids CBs metabolites incense forensics urine urinary herbal blends JWHs JWH018 JWH-018 JWH 18 JWH-18 JWH18 enantiomers phase 1 phase I phase one metabolism enantiomer glucuronidated 32.497115079313
10796 (±)-JWH 018 N-(4-hydroxypentyl) metabolite Exclusive - ≥97% ✓ 2011-05-31 30.827097139518 -jwh-018-n-4-hydroxypentyl-metabolite JWH-018 JWH018 JWH18 JWH-18 JWH18 cannabinoids WIN 55,212-2 urinary metabolites forensics CBs WIN 55212-2 WIN55,212-2 WIN55212-2 monohydroxylation metabolism N-alkyl chains agonists peripheral central receptors smoking mixtures 30.827097139518
10926 (±)-JWH 018 N-(4-hydroxypentyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-06-28 48.189223825681 -jwh-018-n-4-hydroxypentyl-metabolite-d5 JWH-018 JWH018 JWH18 JWH-18 JWH18 cannabinoids WIN 55,212-2 urinary metabolites forensics CBs WIN 55212-2 WIN55,212-2 WIN55212-2 monohydroxylation metabolism N-alkyl chains agonists peripheral central receptors smoking mixtures GC/MS deuteriums standards deuterateds LC/MS GC-MS LC-MS mass spectrometry 48.189223825681
11047 JWH 018 N-(5-bromopentyl) analog New - ≥98% 2012-01-19 32.302845590090 jwh-018-n-5-bromopentyl-analog cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic central peripheral analogs JWH-018 JWH018 JWH 18 JWH18 JWH-18 JWHs herbal blends bromine pentyl chains 32.302845590090
10521 JWH 018 N-(5-chloropentyl) analog New - ≥95% 2012-01-17 45.193105703607 jwh-018-n-5-chloropentyl-analog cannabinoids CBs cannabimimetics CB1 CB2, receptors agonists spices forensics synthetic JWH018 JWH-018 JWH 18 JWH18 JWH-18 JWHs herbal blends analogs chlorine pentyl chains 45.193105703607
9000855 JWH 018 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2010-09-01 112.481585773088 jwh-018-n-5-hydroxypentyl-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 foresnsic science pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite five 5 CBs M-5 M5 smoking mixtures spices cbs synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 112.481585773088
10933 JWH 018 N-(5-hydroxypentyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-06-22 65.383411098240 jwh-018-n-5-hydroxypentyl-metabolite-d5 cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 foresnsic science pain neuroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite two 2 smoking mixtures spices CBs M-5 M5 synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 bath salts LC-MS LC/MS GC-MS GC/MS mass spectrometry MS deuterateds deuteriums agonists selective M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 65.383411098240
10958 JWH 018 N-(5-hydroxypentyl) β-D-Glucuronide Exclusive New - ≥95% ✓ 2011-12-20 55.837719564571 jwh-018-n-5-hydroxypentyl-d-glucuronide JWH-018 JWH018 JWH-18 JWH18 JWHs cannabinoids CBs forensics sciences conjugates metabolites glucuronide incense urine urinary herbal 55.837719564571
9000856 JWH 018 N-pentanoic acid metabolite Exclusive - ≥95% ✓ 2010-09-01 83.447861697431 jwh-018-n-pentanoic-acid-metabolite cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 science pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite 6 six CBs M6 M-6 smoking mixtures spices synthetic JWH018 JWH-018 JWH-18 JWH 18 JWH18 M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 83.447861697431
9000867 JWH 018 N-pentanoic acid metabolite-d4 Exclusive - ≥99% deuterated forms (d1-d4) ✓ 2010-09-15 231.759091679792 jwh-018-n-pentanoic-acid-metabolite-d4 JWH-018 JWH018 deuterateds deuteriums LC-MS LC/MS GC-MS GC/MS mass spectrometry MS cannabinoids receptors WIN 55,212-2 WIN55212-2 WIN 552122 WIN552122 WIN 55,2122 WIN55,2122 CB1 CB2 JWH-018 JWH018 JWH18 JWH-18 JWH18 cannabimimetics urine urinary metabolite glucuroconjugate forensics JWH-018 JWH018 209414-07-3 science pain nueroscience JWH-018-metabolite JWH018-metabolite JWH 018-metabolite 6 six CBs M6 M-6 smoking mixtures spices synthetic M2 M-2 M 2 JWH-018-M2 JWH-018-M-2 JWH-018-M M3 M-3 M 3 JWH-018-M3 JWH-018-M-3 JWH-018-M M4 M-4 M 4 JWH-018-M4 JWH-018-M-4 JWH-018-M M5 M-5 M 5 JWH-018-M5 JWH-018-M-5 JWH-018-M M6 M-6 M 6 JWH-018-M6 JWH-018-M-6 JWH-018-M 231.759091679792
13169 JWH 018 (solution) 209414-07-3 ≥98% 2009-03-12 47.491561336422 jwh-018-solution cannabinoids CB1 CB2 agonists selective receptors WIN 55212-2 JWH-018 JWH018 cbs synthetic JWH 18 JWH-018 JWH18 JWH-18 10900 47.491561336422
13633 JWH 019 209414-08-4 ≥98% 2010-01-14 51.392604445863 jwh-019 cannabinoids CB1 CB2 receptors THC JWH-019 JWH019 Δ9-THC Δ9-tetrahydrocannabinols delta 9 tetrahydrocannabinol cannabinmimetic indoles cannabinoids cbs synthetic JWH019 JWH-019 JWH19 JWH 19 JWH-19 51.392604445863
9000764 JWH 019 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-06 17.245524861878 jwh-019-5-hydroxyindole-metabolite JWH 019-M2 JWH019 JWH-019 JWH-19 JWH 19 JWH19 cannabinoids cannabimimetic metabolites CB1 CB2 receptors agonists spice forensics synthetic smoking urinary urine serum neuroscience CBs 17.245524861878
9000765 JWH 019 N-(6-hydroxyhexyl) metabolite Exclusive - ≥98% ✓ 2011-10-13 23.631270718231 jwh-019-n-6-hydroxyhexyl-metabolite JWH019 JWH-019 JWH-19 JWH 19 JWH19 JWHs cannabinoids cannabimimetic metabolites CB1 CB2 CBs receptors agonists spices forensics synthetic smoking urinary urine serum herbal blends metabolized livers 23.631270718231
10850 JWH 020 Exclusive 209414-09-5 ≥98% ✓ 2011-06-02 42.261104716287 jwh-020 cannabinoids CBs cannabimimetic CB1 receptors agonists CB2 forensics bath salts JWH020 JWH-020 WIN55212-1 WIN55212-2 WIN-55212-1 WIN-55212-2 WIN552121 WIN552122 in vivo JWH 020 42.261104716287
9001056 JWH 022 Exclusive 209414-16-4 ≥98% ✓ 2011-08-09 81.900196852686 jwh-022 AM2201 N-(4-pentenyl) analog JWH022 JWH-022 JWH22 JWH-22 JWHs cannabinoids CBs synthetic standards forensics sciences 81.900196852686
10831 JWH 030 Exclusive 162934-73-8 ≥98% ✓ 2011-10-11 25.915750473185 jwh-030 JWH-030 JWH030 JWH30 JWH-30 JWH30 cannabimimetic cannabinoids synthetics CB1 CB2 CBs receptors forensics neuroscience naphtholyl pyrrole mouse mice inhibits inhibition inhibitors electrically induced vas deferens 25.915750473185
10824 JWH 031 New 162934-74-9 ≥98% 2012-02-17 35.576244985832 jwh-031 JWH-031 JWH031 JWH31 JWH-31 JWH31 JWHs cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic central peripheral mice 35.576244985832
9001201 JWH 072 New 209414-06-2 ≥98% 2012-03-02 43.335915114003 jwh-072 cannabinoids CBs forensics neuroscience cannabimimetic CB1 CB2 receptors spice herbal central peripheral synthetic JWHs JWH072 JWH-072 JWH 72 JWH-72 JWH72 43.335915114003
10904 JWH 073 208987-48-8 ≥97% 2011-05-06 35.953065587533 jwh-073 cannabinoid CB1 CB2 agonist selective receptors WN55212-2 WIN552122 WIN 552122 WIN 55212-2 jwh073 cannabinoids cbs synthetic JWH-073-d7 JWH073-d7 JWH73d7 10904 35.953065587533
10633 JWH 073 2-hydroxyindole metabolite - ≥98% 2011-01-11 31.011945190575 jwh-073-2-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics CBs JWH073 JWH-073 cannabinoids cbs synthetic JWH 73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 31.011945190575
10716 JWH 073 2-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-03-10 13.307377506650 jwh-073-2-hydroxyindole-metabolite-d7 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites monohydroxylated forensics JWH 073 JWH-073 JWH073 JWH73 JWH-73 JWH73 glucuroconjugate JWH-073 JWH073 CBs smoking mixtures spices synthetic LC-MS LC/MS GC-MS GC/MS mass spectrometry MS deuterateds deuteriums standards CBs M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 13.307377506650
10848 JWH 073 2-methylnaphthyl analog Exclusive - ≥98% ✓ 2011-10-11 29.764054293704 jwh-073-2-methylnaphthyl-analog JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetics herbal blends JWH-073 073 JWH73 JWH-73 JWHs 73 29.764054293704
9001014 JWH 073 2'-naphthyl isomer Exclusive - ≥97% ✓ 2011-06-13 11.246485437555 jwh-073-2-naphthyl-isomer JWHs isomers forensic sciences cannabinoids CBs JWH 73 JWH73 JWH-73 JWH073 JWH-073 cannabimimetic receptors Cb1 CB2 agonists spices synthetic herbal blends 11.246485437555
9001016 JWH 073 2'-naphthyl-N-(1-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-28 12.482283404952 jwh-073-2-naphthyl-n-1-methylpropyl-isomer JWH-073 JWH073 JWH-73 JWH73 JWH 73 cannabinoids CBs forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetics 12.482283404952
9001015 JWH 073 2'-naphthyl-N-(2-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-21 10.850114407839 jwh-073-2-naphthyl-n-2-methylpropyl-isomer JWH-073 JWH073 JWH-73 JWH73 JWHs CBs cannabinoids forensic sciences cannabimimetic CB1 CB2 receptors agonists spices synthetic 10.850114407839
9000861 JWH 073 4-hydroxyindole metabolite - ≥98% 2010-09-01 31.007088490801 jwh-073-4-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics JWH 073 Metabolite 1 JWH-073 JWH073 M-1 CBs smoking mixtures spices synthetic standards CBs JWH073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 31.007088490801
10717 JWH 073 4-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-02-21 6.044669013027 jwh-073-4-hydroxyindole-metabolite-d7 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics JWH 073 Metabolite 1 JWH-073 JWH073 M-1 CBs smoking mixtures spices synthetic LC-MS LC/MS GC-MS GC/MS mass spectrometry MS deuterateds deuteriums standards CBs JWH 073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 6.044669013027
9001076 JWH 073 4-methylnaphthyl analog - ≥98% 2011-09-06 34.341054498329 jwh-073-4-methylnaphthyl-analog JWH 122 N-butyl analog; 1-butyl-3-(1-(4-methyl)naphthoyl) indole JWH073 JWH-073 JWH73 JWH-73 analogs hybrids forensics sciences cannabinoids CBs JWHs indoles cannabimimetics JWH 018 122 smoking incense spices forensics pains neuroscience 34.341054498329
9000862 JWH 073 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 26.670627826984 jwh-073-5-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics JWH 073 Metabolite 2 JWH-073 JWH073 CBs M-2 agonists smoking mixtures spices cbs synthetic JWH073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 26.670627826984
10718 JWH 073 5-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-03-11 10.114667254961 jwh-073-5-hydroxyindole-metabolite-d7 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics Metabolite 2 JWH-073 JWH073 M-2 CBs smoking mixtures spices synthetic LC-MS LC/MS GC-MS GC/MS mass spectrometry MS deuterateds deuteriums standards CBs JWH 073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 10.114667254961
9000863 JWH 073 6-hydroxyindole metabolite Exclusive - ≥95% ✓ 2010-09-01 24.845264190709 jwh-073-6-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics JWH 073 Metabolite 3 JWH-073 JWH073 M-3 CBs smoking mixtures spices synthetic JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 24.845264190709
10719 JWH 073 6-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-03-11 5.957007871222 jwh-073-6-hydroxyindole-metabolite-d7 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics JWH 073 Metabolite 3 JWH-073 JWH073 M-3 CBs smoking mixtures spices synthetic LC-MS LC/MS GC-MS GC/MS mass spectrometry MS deuterateds deuteriums standards CBs JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 5.957007871222
9000864 JWH 073 7-hydroxyindole metabolite Exclusive - 98% ✓ 2010-09-01 20.294200571000 jwh-073-7-hydroxyindole-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics JWH 073 Metabolite 4 JWH-073 CBs JWH073 M-4 mixtures smoking spices synthetic JWH 073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 20.294200571000
10720 JWH 073 7-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-07-25 2.962005138349 jwh-073-7-hydroxyindole-metabolite-d7 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites forensics CBs deuterateds deuterium mass spectrometry MS LC/MS LC-MS GC-MS GC/MS WIN55212-2 WIN552122 pain neuroscience JWH 073 JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 2.962005138349
9000868 JWH 073-d7 (solution) Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2010-08-10 34.439604184391 jwh-073-d7-solution deuterateds deuteriums CBs cannabinoids LC-MS LC/MS GC-MS GC/MS mass spectrometry MS standards JWH-073 JWHs JWH073 JWH73 JWH-73 JWH 73 cannabinoids CB1 receptors CB2 peripheral central cbs synthetic JWH073d7 JWH-073-d7 JWH073-d7 JWH73-d7 JWH-73-d7 JWH73-d7 JWH73d7 10905 34.439604184391
9001013 JWH 073 N-(1,1-dimethylethyl) isomer Exclusive New - ≥98% ✓ 2012-01-12 21.552955906945 jwh-073-n-1-1-dimethylethyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWHs JWH073 JWH-073 central peripheral herbal blends butyl chains isomers 21.552955906945
9001012 JWH 073 N-(1-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-22 12.828383284451 jwh-073-n-1-methylpropyl-isomer JWH073 JWH-073 JWH73 JWH-73 forensics sciences cannabinoids CBs JWHs cannabimimetics CB1 CB2 receptors agonists spices synthetic 12.828383284451
9001011 JWH 073 N-(2-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-21 11.158274237773 jwh-073-n-2-methylpropyl-isomer JWH-073 JWH073 JWH-73 JWH73 JWHs CBs cannabinoids forensic sciences cannabimimetic CB1 CB2 receptors agonists spices synthetic 11.158274237773
10795 (±)-JWH 073 N-(3-hydroxybutyl) metabolite Exclusive - ≥98% ✓ 2011-05-31 38.503368091955 -jwh-073-n-3-hydroxybutyl-metabolite JWH-073 JWH073 JWH73 JWH-73 JWH73 cannabinoids metabolites cannabimimetic aminoalkyl chains adulterant CBs metabolism in vitro smoking mixtures 38.503368091955
10927 (±)-JWH 073 N-(3-hydroxybutyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-07-25 34.000722142645 -jwh-073-n-3-hydroxybutyl-metabolite-d5 deuterateds deuterium GC-MS GC/MS LC-MS LC/MS mass spectrometry MS JWH073 JWH73 JWH-073 JWH-73 cannabinoids metabolites cannabimimetic aminoalkyl chains adulterant CBs metabolism in vitro smoking mixtures pain neuroscience 34.000722142645
9000865 JWH 073 N-(4-hydroxybutyl) metabolite Exclusive - ≥98% ✓ 2010-09-01 94.571567053504 jwh-073-n-4-hydroxybutyl-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics JWH 073 Metabolite 5 JWH-073 smoking JWH073 CBs mixtures spices M-5 synthetic JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 94.571567053504
10934 JWH 073 N-(4-hydroxybutyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-10-14 60.928260173248 jwh-073-n-4-hydroxybutyl-metabolite-d5 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M deuterated deuterium metabolites cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugate forensics JWH 073 Metabolite 5 JWH-073 smoking JWH073 CBs mixtures spices 60.928260173248
9000866 JWH 073 N-butanoic acid metabolite Exclusive - ≥98% ✓ 2010-09-01 84.149065798149 jwh-073-n-butanoic-acid-metabolite cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugates forensics JWH 073 Metabolite 6 JWH-073 CBs JWH073 M-6 smoking mixtures spices cbs synthetic JWH-073 JWH073 JWH73 JWH-73 JWH73 M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 84.149065798149
9000870 JWH 073 N-butanoic acid metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2010-09-20 81.275709907057 jwh-073-n-butanoic-acid-metabolite-d5 JWH 073 Metabolite 6-d5 JWH-073 JWH073 cannabinoids CBs receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine urinary metabolites glucuroconjugates forensics synthetic JWH-073 JWH073 JWH73 JWH-73 JWH73 deuterateds deuteriums mass spec GC-MS LC-MS GC/MS LC/MS M2 M-2 M 2 JWH-073-M2 JWH-018-M-2 JWH-073-M M3 M-3 M 3 JWH-073-M3 JWH-073-M-3 JWH-073-M M4 M-4 M 4 JWH-018-M4 JWH-073-M-4 JWH-073-M M5 M-5 M 5 JWH-073-M5 JWH-073-M-5 JWH-073-M M6 M-6 M 6 JWH-073-M6 JWH-073-M-6 JWH-073-M 81.275709907057
13170 JWH 073 (solution) 208987-48-8 ≥97% 2009-03-02 42.977244992795 jwh-073-solution cannabinoid CB1 CB2 agonist selective receptors WN55212-2 WIN552122 WIN 552122 WIN 55212-2 jwh073 cannabinoids cbs synthetic JWH-073-d7 JWH073-d7 JWH73d7 10904 42.977244992795
10579 JWH 081 210179-46-7 ≥98% 2010-10-22 63.246342720480 jwh-081 cannabinoids receptors WIN 55212-2 CB1 CB2 cannabimimetics urine forensics endocannabinoids indoles central peripheral receptors cannabinoids cbs synthetic JWH-081 JWH 81 JWH-81 JWH81 63.246342720480
9001044 JWH 081 2-methoxynaphthyl isomer Exclusive 824960-76-1 ≥98% ✓ 2011-08-23 20.306138663643 jwh-081-2-methoxynaphthyl-isomer JWH 267 JWH-081 JWH081 JWH-81 JWH81 JWHs isomers forensics sciences cannabinoids CBs JWH267 JWH-267 cannabimimetics CB1 CB2 receptors agonists spices synthetics 20.306138663643
9001045 JWH 081 3-methoxynaphthyl isomer Exclusive New - ≥98% ✓ 2012-01-25 28.522489911432 jwh-081-3-methoxynaphthyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWH-081 JWH081 JWH81 JWH-81 JWH 81 central peripheral 28.522489911432
9001046 JWH 081 5-methoxynaphthyl isomer Exclusive - ≥98% ✓ 2011-10-11 18.641213339628 jwh-081-5-methoxynaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic JWH-081 JWH081 JWH-18 JWH48 18 isomers 18.641213339628
9001047 JWH 081 6-methoxynaphthyl isomer Exclusive New 824961-41-3 ≥98% ✓ 2012-01-19 27.884690218810 jwh-081-6-methoxynaphthyl-isomer JWH 166 cannabinoids CBs cannabimimetics central CB1 CB2 peripheral receptors agonists spices forensics synthetic isomers methoxy groups naphthyl rings research JWH081 JWH-081 JWH 81 JWH-81 JWH81 JWH166 JWH-166 JWHs 27.884690218810
9001048 JWH 081 7-methoxynaphthyl isomer Exclusive 824961-61-7 ≥98% ✓ 2011-10-11 19.629397573782 jwh-081-7-methoxynaphthyl-isomer JWH 164 JWH 164 JWH164 JWH-164 cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic JWH-081 JWH081 JWH-81 JWH81 81 isomers 19.629397573782
10511 JWH 081-d9 - ≥99% deuterated forms (d1-d9) 2011-09-08 34.895498379446 jwh-081-d9 cannabinoids receptors WIN 55212-2 CB1 CB2 cannabimimetics urine forensics endocannabinoids indoles central peripheral receptors cannabinoids CBs synthetic JWH-081 JWH 81 JWH-81 JWH81 standards deuterated deuterium mass spectrometry LC-MS LC/MS GC-MS GC/MS MS 34.895498379446
9000768 JWH 081 N-(5-hydroxypentyl) metabolite Exclusive - ≥95% ✓ 2011-08-05 33.587906619445 jwh-081-n-5-hydroxypentyl-metabolite JWH-081 JWH081 JWH-81 JWH81 JWH 81 JWHs CBs cannabinoids forensics sciences metabolites cannabimimetics metabolites CB1 CB2 receptors agonists spices synthetics smoking urinary urine serum 33.587906619445
10680 JWH 098 Exclusive 316189-74-9 ≥98% ✓ 2011-04-20 38.943367530193 jwh-098 JWH-098 JWH98 JWH-98 JWH 98 cannabinoids cannabimimetics CBs CB1 receptors agonists CB2 pain spice forensics synthetic naphthalen-1-yl-(1-pentylindol-3-yl)methanone 1-propyl-2-methyl-3-(1-naphthoyl)indole 1,1-dimethylbutyl-1-deoxy-Delta(9)-THC 1-pentyl-3-(1-naphthoyl)indole naphthalenes JWH 133 JWH133 JWH-133 JWH-018 JWH018 JWH 018 JWH18 JWH015 JWH15 JWH 015 JWH-015 indoles 38.943367530193
10591 JWH 122 619294-47-2 ≥98% 2010-12-15 91.021638971897 jwh-122 JWHs JWH-122 JWH122 cannabinoids CB1 CB2 CBs 1 2 CB-1 CB-2 receptors potent synthetic forensics pain central peripheral cannabinoids cbs synthetic 91.021638971897
9001032 JWH 122 2-methylnaphthyl isomer Exclusive New - ≥98% ✓ 2012-05-16 249.235232469323 jwh-122-2-methylnaphthyl-isomer JWH-122 JWH122 JWHs isomers forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics 249.235232469323
9001033 JWH 122 3-methylnaphthyl isomer - ≥98% 2011-11-08 104.035829239431 jwh-122-3-methylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic synthetic herbal methyl naphthyl isomers JWH122 JWH-122 JWHs 104.035829239431
9001034 JWH 122 5-methylnaphthyl isomer - ≥98% 2011-11-08 103.417044709044 jwh-122-5-methylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic JWHs JWH122 JWH-122 synthetic herbal methyl naphthyl isomers central peripheral 103.417044709044
9001035 JWH 122 6-methylnaphthyl isomer Exclusive New - ≥95% ✓ 2012-05-16 255.662939793352 jwh-122-6-methylnaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetics herbal blends isomers JWH-122 JWH122 255.662939793352
9001036 JWH 122 7-methylnaphthyl isomer Exclusive New 824960-56-7 ≥98% ✓ 2012-05-16 264.137606460019 jwh-122-7-methylnaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic herbal blends isomers JWH-122 JWH122 264.137606460019
9001037 JWH 122 8-methylnaphthyl isomer Exclusive New - ≥98% ✓ 2012-05-16 187.170934667690 jwh-122-8-methylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic JWH-122 JWH122 herbalmethyl groups naphthyl rings herbal 187.170934667690
10512 JWH 122-d9 - ≥99% deuterated forms (d1-d9) 2011-09-08 82.701417264663 jwh-122-d9 JWHs JWH-122 JWH122 cannabinoids CB1 CB2 CBs CB-1 CB-2 receptors potent synthetic forensics pain central peripheral cannabinoids CBs synthetic standards deuterated deuterium mass spectrometry LC-MS LC/MS GC-MS GC/MS MS 82.701417264663
11784 JWH 122 N-(4-hydroxypentyl) metabolite Exclusive New - ≥98% ✓ 2012-05-21 177.343209960627 jwh-122-n-4-hydroxypentyl-metabolite cannabinoids forensics CB1 CB2 metabolites metabolism designer drugs neuroscience CBs JWH-210 JWH210 JWH122 JWH-122 serum urine 177.343209960627
11611 JWH 122 N-(4-pentenyl) analog Exclusive New - ≥98% ✓ 2012-04-20 169.727469987228 jwh-122-n-4-pentenyl-analog MAM2201 N-(4-pentenyl) analog; JWH 022 4-methylnaphthyl analog cannabinoids CBs forensics CB1 CB2 analogs designer drugs JWH122 neuroscience JWH-122 synthetics central peripheral MAM2201 JWH 022 JWH022 JWH-022 169.727469987228
10925 JWH 122 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-06-17 62.067860111477 jwh-122-n-5-hydroxypentyl-metabolite MAM2201 N-(5-hydroxypentyl) metabolite cannabinoids CBs receptors CB1 CB2 cannabimimetics analogs forensics JWH122 JWH-122 monohydroxylation N-alkyl chains naphthoylindole JWH 018 JWH018 JWH-018 JWH18 JWH-18 JWH 18 JWH073 JWH-073 JWH 073 JWH73 JWH-73 JWH 73 62.067860111477
11475 JWH 122 N-(5-hydroxypentyl) metabolite-d5 Exclusive New - ≥99% deuterated forms (d1-d5) ✓ 2012-04-27 177.815253720284 jwh-122-n-5-hydroxypentyl-metabolite-d5 MAM2201 N-(5-hydroxypentyl) metabolite-d5 LC-MS LC/MS GC-MS GC/MS mass spectrometry MS cannabinoids cbs synthetic receptors CB1 CB2 cannabimimetics analogs forensics JWH122 JWH-122 monohydroxylation N-alkyl chains naphthoylindole JWH 018 JWH018 JWH-018 JWH18 JWH-18 JWH 18 JWH073 JWH-073 JWH 073 JWH73 JWH-73 JWH 73 177.815253720284
10825 JWH 145 Exclusive 914458-19-8 ≥95% ✓ 2011-11-10 24.008926127631 jwh-145 JWH-145 JWH145 JWHs cannabinoids CBs CB1 CB2 herbals smoking forensics receptors agonists cannabimimetic aminoalkylindole JWH018 JWH-018 JWH 018 blends 73 18 JWH073 JWH-073 JWH 073 JWH73 JWH 73 JWH-73 JWH18 JWH-18 24.008926127631
10826 JWH 147 New 914458-20-1 ≥95% 2012-03-06 38.607296567102 jwh-147 JWH147 JWH-147 JWHs CBs smoking receptors agaonists aminoalkylindoles cannabinoids central peripheral cannabimimetic CB1 CB2 spices forensics neuroscience pain herbal 38.607296567102
11201 JWH 175 Exclusive New 619294-35-8 ≥98% ✓ 2012-02-09 33.281770722897 jwh-175 CBs JWH-175 JWH175 JWHs CB1 CB2 cannabinoids JWH018 JWH-018 JWH 018 receptors agonist spices synthetic 33.281770722897
9001205 JWH 180 New 824959-87-7 ≥98% 2012-03-26 67.051033200285 jwh-180 JWH-180 JWH180 cannabinoids CBs designer drugs cannabimimetics CB1 CB2 receptors agonists herbals blends synthetics central peripheral forensics 67.051033200285
10643 JWH 182 Exclusive 824960-02-3 ≥97% ✓ 2011-10-11 37.014994360320 jwh-182 JWH-182 JWHs CB1 CB2 CBs receptors agonists pains spices forensics synthetics cannabinoids cells animals 37.014994360320
10902 JWH 200 103610-04-4 ≥98% 2011-05-05 23.047589726815 jwh-200 cannabinoids receptors agonists CB1 pain antinociception cannabinoids cbs synthetic JWH200 JWH-200 10902 23.047589726815
9000897 JWH 200 2'-naphthyl isomer Exclusive 133438-66-1 ≥98% ✓ 2011-06-20 14.291077348066 jwh-200-2-naphthyl-isomer JWH200 JWH-200 CBs cannabinoids forensics sciences cannabimimetic CB1 receptors agonist spices synthetic 14.291077348066
10744 JWH 200 4-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-04-15 29.918738489871 jwh-200-4-hydroxyindole-metabolite JWH-200 JWH200 cannabinoids receptors agonists pain antinociception CBs cannabimimetic metabolites CB1 CB2 spices forensics synthetic smoking urinary urine 29.918738489871
10745 JWH 200 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-06 19.416322020521 jwh-200-5-hydroxyindole-metabolite JWH-200 JWH200 cannabinoids receptors agonists pain antinociception CBs cannabimimetic metabolites CB1 CB2 spices forensics synthetic smoking urinary urine neuroscience 19.416322020521
10746 JWH 200 6-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-10-11 25.816933701657 jwh-200-6-hydroxyindole-metabolite JWH200 JWH-200 cannabinoids cannabimimetic metabolites CB1 CB2 CBs receptors agonists spices forensics synthetics smoking urinary urine aminoalkylindoles binds binding high-affinity high affinity JWHs 25.816933701657
10747 JWH 200 7-hydroxyindole metabolite - ≥98% 2011-11-21 16.661862667718 jwh-200-7-hydroxyindole-metabolite JWH200 JWH-200 cannabinoids cannabimimetics metabolites CB1 CB2 CBs receptors agonists spices forensics synthetic smoking urinary urine aminoalkylindole JWH 015 JWH 018 JWH015 JWH018 JWH-015 JWH-018 JWH15 JWH18 JWH 15 JWH 18 JWH-15 JWH-18 16.661862667718
10903 JWH 200-d5 - ≥99% deuterated forms (d1-d5) 2011-05-06 7.401256906077 jwh-200-d5 cannabinoids receptors agonists CB1 pain antinociception deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS cannabinoids cbs synthetic JWH-200-d5 JWH200-d5 10903 7.401256906077
10682 JWH 200-d5 (solution) - ≥99% deuterated forms (d1-d5) 2011-01-07 35.027270718231 jwh-200-d5-solution cannabinoids receptors agonists CB1 pain antinociception deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS cannabinoids cbs synthetic JWH-200-d5 JWH200-d5 10903 35.027270718231
13171 JWH 200 (solution) 103610-04-4 ≥98% 2009-03-25 42.655236723869 jwh-200-solution cannabinoids receptors agonists CB1 pain antinociception cannabinoids cbs synthetic JWH200 JWH-200 10902 42.655236723869
10721 JWH 201 Exclusive 864445-47-6 ≥98% ✓ 2011-02-24 52.971855179095 jwh-201 cannabinoids CB1 CB2 receptors CBs JWH201 JWH-201 JWH250 JWH-250 JWH 250 52.971855179095
9000736 JWH 203 864445-54-5 ≥98% 2011-02-21 60.724386917343 jwh-203 cannabinoids receptors JWH 250 JWH203 JWH-203 CB1 CB2 cannabimimetics forensics pain CBs binding analgesic 60.724386917343
10868 JWH 203 3-chlorophenyl isomer Exclusive 864445-56-7 ≥98% ✓ 2011-06-03 27.553149171271 jwh-203-3-chlorophenyl-isomer JWH 237; JWH 203 3-chloro isomer cannabinoids receptors JWH 250 JWH203 JWH-203 CB1 CB2 CBs cannabimimetics forensics pain bath salts phenylacetylindole analog 27.553149171271
10867 JWH 203 4-chlorophenyl isomer Exclusive 864445-58-9 ≥98% ✓ 2011-06-02 35.659226519337 jwh-203-4-chlorophenyl-isomer JWH 206; JWH 203 4-chloro isomer cannabinoids CB1 CB2 receptors synthetic forensics pain bath salts CBs JWH203 JWH-203 JWH206 JWH-206 35.659226519337
10644 JWH 210 824959-81-1 ≥98% 2011-02-01 91.721299146051 jwh-210 cannabimimetic cannabinoids alklyindoles CB1 CB2 receptors agonists CBs JWH-210 JWH210 91.721299146051
9001038 JWH 210 2-ethylnaphthyl isomer Exclusive - ≥98% ✓ 2011-10-11 13.341907063722 jwh-210-2-ethylnaphthyl-isomer JWHs cannabinoids cannabimimetic metabolites CB1 CB2 CBs receptors agonists spices forensics synthetics smoking urinary urine serums JWH-210 JWH210 alkyindoles herbal blends 13.341907063722
9001039 JWH 210 3-ethylnaphthyl isomer Exclusive New - ≥98% ✓ 2011-11-30 15.530770432025 jwh-210-3-ethylnaphthyl-isomer cannabinoids CBs cannabimimetic metabolites receptors agonists spices forensics synthetic smoking urinary urine serum JWHs JWH210 JWH-210 alkylindole herbal blends isomers ethyl chains naphthyl groups 15.530770432025
9001040 JWH 210 5-ethylnaphthyl isomer Exclusive - ≥98% ✓ 2011-11-17 15.487964321381 jwh-210-5-ethylnaphthyl-isomer cannabinoids cannabimimetics metabolites CB1 CB2 CBs receptors agonists spices forensics synthetic smoking urinary urine serum alkylindoles herbal blends isomers JWH-210 JWH210 15.487964321381
9000771 JWH 210 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-08-10 14.867951564468 jwh-210-5-hydroxyindole-metabolite JWH-210 JWH210 cannabinoids CBs cannabimimetic metabolites CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum 14.867951564468
9001041 JWH 210 6-ethylnaphthyl isomer Exclusive New - ≥98% ✓ 2012-01-31 27.473526939369 jwh-210-6-ethylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic smoking JWH210 JWH-210 JWHs isomers alkylindoles extracts herbal blends 27.473526939369
9001042 JWH 210 7-ethylnaphthyl isomer Exclusive 824960-64-7 ≥98% ✓ 2011-10-11 15.493589635294 jwh-210-7-ethylnaphthyl-isomer JWH 234 JWHs cannabinoids cannabimimetic metabolites CB1 CB2 CBs receptors agonists spices forensics synthetic smoking urinary urine serums JWH-234 JWH234 JWH-210 JWH210 alkylindoles herbal blends 15.493589635294
9001043 JWH 210 8-ethylnaphthyl isomer Exclusive - ≥95% ✓ 2011-11-04 12.948135089839 jwh-210-8-ethylnaphthyl-isomer JWH210 JWH-210 cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum herbal alkylindole isomers naphthyl groups 12.948135089839
10510 JWH 210-d9 - ≥99% deuterated forms (d1-d9) 2011-09-08 28.281393228426 jwh-210-d9 cannabimimetic cannabinoids alklyindoles CB1 CB2 receptors agonists CBs JWH-210 JWH210 JWHs standards deuterated deuterium mass spectrometry LC-MS LC/MS GC-MS GC/MS MS pain 28.281393228426
10940 JWH 210 N-(4-hydroxypentyl) metabolite New - ≥95% 2012-01-19 31.847586683177 jwh-210-n-4-hydroxypentyl-metabolite cannabinoids CBs cannabimimetics metabolites receptors agonists spices forensics synthetic smoking urinary urine serum JWH210 JWH-210 JWHs alkylindoles liver 31.847586683177
10941 JWH 210 N-(5-carboxypentyl) metabolite Exclusive - ≥98% ✓ 2011-10-11 28.047369688706 jwh-210-n-5-carboxypentyl-metabolite JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetics smoking urinary urine serums JWH-210 210 liver excreted 28.047369688706
9000772 JWH 210 N-(5-hydroxypentyl) metabolite - ≥98% 2011-11-04 17.738441468544 jwh-210-n-5-hydroxypentyl-metabolite JWH 210 JWH210 cannabinoids CBs JWHs alkylindoles liver cannabimimetic metabolites CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum 17.738441468544
11153 JWH 249 New 864445-60-3 ≥98% 2012-02-10 28.643596557285 jwh-249 cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWH249 JWH-249 JWHs central peripheral 28.643596557285
13634 JWH 250 864445-43-2 ≥98% 2010-01-14 81.333491122734 jwh-250 cannabinoids CB1 CB2 receptors THC JWH-250 JWH250 Δ9-THC Δ9-tetrahydrocannabinols delta 9 tetrahydrocannabinols indoles cbs synthetic 81.333491122734
9000766 JWH 250 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-20 46.724391608983 jwh-250-5-hydroxyindole-metabolite JWH250 JWH-250 cannabinoids CBs cannabimimetics metabolite CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum 46.724391608983
10661 JWH 250-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-02-14 37.389532481263 jwh-250-d5 cannabinoids receptors agonists CB1 pain antinociception deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS cannabinoids cbs synthetic JWH-250-d5 JWH250-d5 37.389532481263
10939 JWH 250 N-(4-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-10-24 54.240961699935 jwh-250-n-4-hydroxypentyl-metabolite JWHs JWH-250 JWH250 metabolites cannabinoids CB1 CB2 CBs herbal smoke smoking forensics receptors agonist cannabimimetic metabolite metabolism 54.240961699935
10938 JWH 250 N-(5-carboxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-19 69.224958016694 jwh-250-n-5-carboxypentyl-metabolite JWHs JWH-250 JWH250 metabolites forensics sciences urinary urine synthetics cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics smoking urinary urine serum 69.224958016694
9000767 JWH 250 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-08-05 56.847280509968 jwh-250-n-5-hydroxypentyl-metabolite JWH250 JWH-250 forensic sciences CBs cannabinoids JWHs cannabimimetics metabolites CB1 CB2 receptors agonists spices forensics synthetics smoking urinary urine serum 56.847280509968
11474 JWH 250 N-(5-hydroxypentyl) metabolite-d5 Exclusive New - ≥99% deuterated forms (d1-d5) ✓ 2012-04-27 122.875777105692 jwh-250-n-5-hydroxypentyl-metabolite-d5 deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS synthetic JWH250 JWH-250 forensic sciences CBs cannabinoids JWHs cannabimimetics metabolites CB1 CB2 receptors agonists spices forensics synthetics smoking urinary urine serum JWH-18 JWH 18 JWH18 JWH018 JWH-018 JWH 018 JWH 15 JWH-15 JWH15 JWH015 JWH-015 JWH 015 122.875777105692
10578 JWH 251 864445-39-6 ≥98% 2010-08-20 44.132323069158 jwh-251 cannabinoids receptors JWHs JWH-251 JWH251 WIN55212-2 WIN 55212-2 CB1 CB2 cannabimimetics urine forensics cannabinoids cbs synthetic 44.132323069158
9001021 JWH 251 3-methylphenyl isomer Exclusive - ≥98% ✓ 2011-10-11 19.794696132596 jwh-251-3-methylphenyl-isomer JWH 251 3-methyl isomer cannabinoids receptors CB1 CB2 CBs WIN55212-2 WIN-552122 WIN-55212-2 WIN 55,2122 WIN 55,212-2 cannabimimetics urine forensic JWH-251 JWH251 adulterant 19.794696132596
9001022 JWH 251 4-methylphenyl isomer Exclusive 864445-41-0 ≥98% ✓ 2011-10-14 10.688563535911 jwh-251-4-methylphenyl-isomer JWH 251 4-methyl isomer JWH-251 JWH251 CBs cannabinoids receptors WIN 55212-2 WIN55212 WIN 55,212-2 WIN 55,2122 CB1 CB2 cannabimimetics urine forensics 10.688563535911
10722 JWH 302 Exclusive 864445-45-4 ≥95% ✓ 2011-03-04 58.664660429136 jwh-302 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine forensics CBs JWH302 JWH-302 indoles central peripheral GTPγS binding 58.664660429136
10797 JWH 307 New 914458-26-7 ≥96% 2011-12-15 54.650958008575 jwh-307 JWH307 JWH-307 cannabinoids CBs CB1 CB2 herbal smoking forensics receptors agonists JWHs cannabimimetic psychological neurological nuerology toxicological toxicology 54.650958008575
10830 JWH 309 Exclusive New 914458-42-7 ≥98% ✓ 2012-02-28 31.150459420982 jwh-309 JWH309 JWH-309 cannabinoids forensic science neuroscience cannabimimetic CB1 CB2 receptors spices herbal central peripheral 31.150459420982
10829 JWH 368 New 914458-31-4 ≥98% 2011-12-14 35.244410394511 jwh-368 JWH368 JWH-368 cannabinoids CBs CB1 CB2 herbal smoking forensics sciences receptors agonists cannabimimetic JWHs 35.244410394511
10828 JWH 369 New 914458-27-8 ≥95% 2012-01-25 28.568664451965 jwh-369 JWH369 JWH-369 cannabinoids cannabimimetics CB1 CB2 CBs receptors agonists spices forensics synthetic central peripheral mouse research 28.568664451965
10827 JWH 370 914458-22-3 ≥95% 2011-11-10 23.615292190691 jwh-370 JWH370 JWH-370 JWHs cannabinoids CB1 CB2 herbal smoking forensics receptors agonists cannabimimetic aminoalkylindole JWH 018 JWH 18 JWH-018 JWH018 JWH073 JWH 73 JWH 073 JWH-073 analogs blends JWH-73 JWH73 JWH-18 JWH18 23.615292190691
13636 JWH 398 Exclusive - ≥95% ✓ 2010-10-22 75.850922185528 jwh-398 jwh398 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine forensics CBs JWH-398 cbs synthetic 75.850922185528
9001023 JWH 398 2-chloronaphthyl isomer - ≥95% 2011-11-09 13.148088908318 jwh-398-2-chloronaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic herbal mixtures isomers chloro naphthyl JWH398 JWH-398 JWHs 13.148088908318
9001024 JWH 398 3-chloronaphthyl isomer Exclusive New - ≥98% ✓ 2012-01-11 20.466262453979 jwh-398-3-chloronaphthyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWH398 JWH-398 JWHs isomers herbal mixtures chlorine naphthyl rings central peripheral 20.466262453979
9001025 JWH 398 5-chloronaphthyl isomer Exclusive - ≥98% ✓ 2011-08-23 17.593459146997 jwh-398-5-chloronaphthyl-isomer JWH398 JWH-398 forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics central peripheral 17.593459146997
9001026 JWH 398 6-chloronaphthyl isomer Exclusive - ≥98% ✓ 2011-11-04 17.018972886219 jwh-398-6-chloronaphthyl-isomer JWH398 JWH-398 cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic isomers herbal mixtures chloro groups naphthyl rings 17.018972886219
9001027 JWH 398 7-chloronaphthyl isomer - ≥98% 2011-11-16 17.360886500225 jwh-398-7-chloronaphthyl-isomer cannabinoids cannabimimetics CBs CB1 CB2 receptor agonists spices forensics synthetic JWHs JWH398 JWH-398 isomers herbal chloro groups naphthyl rings 17.360886500225
9001028 JWH 398 8-chloronaphthyl isomer Exclusive New - ≥98% ✓ 2012-01-13 23.049348494365 jwh-398-8-chloronaphthyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic isomers herbal mixtures JWHs JWH-398 JWH398 central peripheral 23.049348494365
10514 JWH 398-d9 Exclusive - ≥99% deuterated forms (d1-d9) ✓ 2011-08-25 38.562490444706 jwh-398-d9 JWH398 JWH-398 standards cannabinoids CBs JWHs forensics sciences deuterateds deuterium GC/MS GC-MS LC/MS LC-MS mass spectrometry MS 38.562490444706
9000770 JWH 398 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-06 22.685776002988 jwh-398-n-5-hydroxypentyl-metabolite JWH398 cannabinoids CBs JWH-398 forensic sciences JWHs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetics 22.685776002988
9001203 JWH 424 New - ≥98% 2012-02-27 32.938874205072 jwh-424 cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWHs JWH424 JWH-424 JWH018 JWH-018 JWH 18 JWH-18 JWH18 herbal blends 32.938874205072
13158 JZL 184 1101854-58-3 ≥97% 2009-01-26 215.123167587476 jzl-184 2-AG 2AG MAGL inhibitors inhibits inhibition endocannabinoids pains analgesia MGL inhibitor JZL184 JZL-184 cannabinoids 215.123167587476
13668 JZL 195 121004-12-8 ≥98% 2010-02-10 222.909116022099 jzl-195 fatty acid amide hydrolase FAAH monoacylglycerol lipase MAGL endocannabinoids arachidonoyl ethanolamide AEA 2-arachidonoylglycerol 2-AG inibitors inhibition inhibits PF-3845 PF 3845 PF3845 JZL195 JZL-195 JZL184 antinociception pain catalepsy hypomotility CB1 2AG cannabinoids inhibitors cbs sythetic Methylenedioxybenzenes 1,3-Dioxaindans 1,3 Dioxaindans 1,3-Dioxindans 1,3 Dioxindans Benzodioxoles 222.909116022099
10640 KM 233 Exclusive 628263-22-9 ≥98% ✓ 2011-07-07 30.745445845929 km-233 KM233 KM-233 CBs cannabinoids CB2 agonists recptors CB1 gliomas anti tumors cancers 30.745445845929
10009280 L-759,633 174627-50-0 >98% 2007-09-13 33.291215469613 l-759-633 L759633 cannabinoids receptors agonists CB1 CB2 endocrinology neurochemistry cannabinoids cbs synthetic 33.291215469613
10008618 Lauric Acid Leelamide - >98% 2006-09-05 0.377171270718 lauric-acid-leelamide saturated fatty acids synthesized synthesis plants animals acetyl coenzymes CoA energy storage 12-carbons coconut nut oils COX-2 cyclooxygenase-2 cyclooxygenases expressions C:8-18 inhibitors inhibits inhibition pyruvate dehydrogenases kinases diterpene Sanskrit CB1 CB2 cannbinoids receptors central peripheral tertiary 3H CP55940 PDK antiinflammatory anti-inflammatory PLA2 phospholipases inflammation dehydroabietylamine leelamine cannabinoids cbs synthetic 0.377171270718
10006148 Leelamine 1446-61-3 >98% 2006-05-10 0.274861878453 leelamine Dehydroabietylamine inhibitors inhibits inhibition pyruvate dehydrogenases kinases diterpene Sanskrit CB1 CB2 cannbinoids receptors central peripheral tertiary 3H CP55940 PDK antiinflammatory anti-inflammatory PLA2 phospholipases inflammation dehydroabietylamine cannabinoids cbs synthetic 0.274861878453
10008614 Leelamine (hydrochloride) - ≥98% 2006-05-10 0.154696132596 leelamine-hydrochloride Dehydroabietylamine inhibitors inhibits inhibition pyruvate dehydrogenases kinases diterpene Sanskrit CB1 CB2 cannbinoids receptors central peripheral tertiary 3H CP55940 PDK antiinflammatory anti-inflammatory PLA2 phospholipases inflammation dehydroabietylamine cannabinoids cbs synthetic 0.154696132596
13453 LH 21 611207-11-5 ≥98% 2011-03-22 20.343434622468 lh-21 cannabimimetic CBs cannabinoids CB1 receptors antagonists pain weight gain obesity LH-21 LH21 central 20.343434622468
9001219 MAM2201 Exclusive New 1354631-24-5 ≥98% ✓ 2012-03-28 330.627994973750 mam2201 AM2201 4-methylnaphthyl analog; JWH 122 N-(5-fluoropentyl) analog cannabinoids CBs CB1 CB2 cannabimimetics receptors herbals spices designer drugs AM-2201 AM 2201 MAM-2201 MAM 2201 analogs synthetics central peripheral forensics JWH122 JWH 122 JWH-122 330.627994973750
10563 MDA 19 1048973-47-2 ≥95% 2010-09-17 47.691606156274 mda-19 agonists cannabinoids CB2 CB1 pains 1104302-26-2 tactile allodynia paclitaxel spinal nerves ligation MDA-19 MDA19 CBs peripheral central MDAs central cannabinoids cbs synthetic cannabinoids Epidermal Growth Factor Receptor Protein-Tyrosine Kinase Receptors, Epidermal Growth Factor-Urogastrone Receptor Transforming Growth Factor alpha Transforming Growth Factor alpha Receptor Epidermal Growth Factor Receptor Kinase Receptor Epidermal Growth Factor Receptor erbB 1 Proto Oncogene Protein Receptor Urogastrone Urogastrone Receptor Receptor TGF alpha TGF-alpha Receptor c-erbB-1 Protein Proto-Oncogene Receptor EGF EGF Receptor 47.691606156274
10639 MDA 77 Exclusive 1103774-21-5 ≥98% ✓ 2011-05-16 2.672099447514 mda-77 CB2 inverse agonists inflammation pain CB1 CBs cannabinoids peripheral MDA77 MDA-77 in vivo binds binding assay 2.672099447514
10979 MDMA methylene homolog (hydrochloride) Exclusive - ≥98% ✓ 2011-06-22 31.106511302061 mdma-methylene-homolog-hydrochloride 3,4-Methylenedioxymethamphetamine methyl homolog forensic sciences cannabinoids CBs pyrovalerones pentylones designer drugs forensics neuroscience psychoactive ecstasy HCl 31.106511302061
10007704 N-(3-hydroxyphenyl)-Arachidonoyl amide Exclusive 183718-75-4 >98% ✓ 2007-02-02 9.847955801105 n-3-hydroxyphenyl-arachidonoyl-amide 3-HPAA neurochemistry neuroscience AM404 anologs N-(4-hydroxyphenyl)-arachidonoylamides AEA ethanolamides cycloxygenase-1 cyclooxygenase-2 COX-1 COX-2 inhibits inhibitors inhibition N-(3-hydroxyphenyl)-Arachidonoylamide 3-HPA cannabinoids cbs synthetic 9.847955801105
10007431 N-Arachidonoyl Dopamine-d8 - ≥99% deuterated forms (d1-d8) 2005-08-10 10.190939226519 n-arachidonoyl-dopamine-d8 NADA-d8 deuterateds analogs capsaicin arachidonic acids amides VR1 receptors vannilloids cannabinoids ada cb1 cb2 analgesic arachidonoyl-dopamine neurochemistry neuroscience deuterated deuterium GC/MS GC-MS LC/MS LC-MS mass 10007431 spectrometry cannabinoids cbs synthetic 10.190939226519
10005455 N-Arachidonoyl-L-Serine 187224-29-9 >98% 2004-08-11 7.062702159718 n-arachidonoyl-l-serine ARA-S endocannabinoids antagonists cannabidiols neuroprotective neurotransmitters hypotensive effects antagonize antagonist neurochemistry neuroscience cannabinoids cbs synthetic 7.062702159718
10005609 N-Oleoyl Taurine Exclusive 52514-04-2 ≥98% ✓ 2005-01-05 7.001404235727 n-oleoyl-taurine endocannibinoids fatty amides oleamides taurines amino-acyls lipidomics profiling fatty acids neurochemistry neuroscience TRPV1 TRPV4 FAAH cannabinoids cbs synthetic 7.001404235727
10006803 O-1602 317321-41-8 >98% 2005-09-12 11.877928176795 o-1602 abnormal cannabidiols CB1 CB2 receptors vasorelaxation neurochemistry neuroscience central cannabinoids peripheral selective antagonists nonendothelium-dependant vasodilation nitric oxides NOs inhibits inhibitors inhibition vasorelaxant cannabinoids cbs synthetic 11.877928176795
10006804 O-1821 35482-50-9 >97% 2005-09-12 26.649907918968 o-1821 abnormal cannabidiol central cannabinoids peripheral CB1 CB2 receptors vasorelaxation neurochemistry neuroscience antagonists synthetic regioisomer endothelium dependent vasodilation cannabinoids cbs synthetic 26.649907918968
10004914 O-1918 536697-79-7 >98% 2005-09-09 11.646172059984 o-1918 antagonists abnormal cannabinoids cannabidiols cannabidiol-mediated synthetic regioisomers CB1 CB2 responsiveness psychotropics activity induces endothelium-dependent vasodilations NO-independent nitric oxides mechanisms analogs endothelial receptors inhibits inhibition inhibitors vasorelexants in vitro blocks induced activations PI3-kinases Akt pathway umbilical vein cells neuroscience neurochemistry O1918 0-1918 cannabinoids cbs synthetic 11.646172059984
10009195 O-2545 (hydrochloride) - ≥98% 2007-07-12 5.521546961326 o-2545-hydrochloride cannabinoids water soluble agonists receptors CB1 CB2 lipophilic surfactants 874745-42-3 murine models intravenously IV 02545 intracerebroventricularly endocrinology neurochemistry cannabinoids cbs synthetic 5.521546961326
10007823 Oleoyl Ethanolamide-d2 - ≥99% deuterated forms (d1-d2) 2006-03-06 17.913535911602 oleoyl-ethanolamide-d2 OEA-d2; Oleic Acid Ethanolamide-d2 GC/MS deuteriums isotopes internal standards deuterateds LC/MS GC-MS LC-MS mass spectrometry cannabinoids neurotransmitter chocolate fatty acids neurochemistry neuroscience ethanolamines ethanolamides cbs synthetic 17.913535911602
9000552 Oleoyl Ethanolamide-d4 Exclusive - ≥99% deuterated forms (d1- d4) ✓ 2010-01-12 10.248737174428 oleoyl-ethanolamide-d4 Oleic Acid Ethanolamide-d4; OEA-d4 cannabinoids neurotransmitter chocolate fatty acids neurochemistry neuroscience ethanolamines ethanolamides deuterateds deuteriums MS mass spectrometry CBs LC-MS OEAs LC/MS GC/MS G-MS standards PPAR brain tissue neurochemistry neuroscience synthetic 10.248737174428
10005459 Oleoyl Ethyl Amide Exclusive 85075-82-7 >98% ✓ 2004-07-21 22.870906077348 oleoyl-ethyl-amide N-Ethyloleamide; OEtA endocannabinoids analogs FAAH fatty acid amide hydrolase analgesic inhibitors inhibitor inhibition acyl PEAase anxiolytic inhibits selective selectivity neuroscience neurochemistry cannabinoids cbs synthetic 22.870906077348
10965 Palmitoleoyl Ethanolamide 94421-67-7 ≥98% 2011-06-27 20.839465930018 palmitoleoyl-ethanolamide POEA cannabinoids endocannabinoids CBs N-acylethanolamines signalling N-acylethanolamides NAEs signaling receptors pain lipid-derived 20.839465930018
13279 PF-3845 1196109-52-0 ≥98% 2010-01-27 43.794327808471 pf-3845 fatty acids hydrolase FAAH N-acyl ethanolamines NAEs endocannabinoids N-arachidonoyl ethanolamine anandamide AEA inhibitors inhibits inflammation pain PF3845 PF 3845 cannabinoids cbs synthetic Antibodies Monoclonal Monoclonal Antibodies 43.794327808471
71655 PHOP 288862-83-9 >98% 2005-02-02 8.605465666929 phop Phenyl hexanoyl oxazolopyridine; CAY10402 FAAH fatty acids amides hydrolases inhibits inhibitors inhibition cannabinoids CB1 CB2 hydrolysis hydrolyze CAY-10402 TGH triacylglycerols neurochemistry neuroscience cbs synthetic 8.605465666929
10006973 Pravadoline 92623-83-1 ≥98% 2011-02-08 49.868317154124 pravadoline WIN 48,098 Anti-inflammatory analgesic COX inhibitors pain AAI NSAIDs inhibits inhibition prostaglandins PGs synthesis murine inhibited mouse cyclooxygnases opoid Indoles receptors WIN48098 WIN-48098 WIN 48098 WIN-48,8098 49.868317154124
13621 Pristimerin Exclusive 1258-84-0 ≥98% ✓ 2010-03-08 49.274348855564 pristimerin Celastrol methyl ester; NSC 99281 monoacylglycerol lipases MAGLs monoglycerol MGLs cannabinoids 2-arachidonoyl glycerol 2-AG inhibitor 2-Picenecarboxylic acids cannabinoids cbs synthetic Triterpenes 49.274348855564
12015 Prostaglandin D2-1-glyceryl ester 309260-52-4 >95% (as a 9:1 mixture of the 1- and 2-glyceryl esters) 2004-08-05 35.810524861878 prostaglandin-d2-1-glyceryl-ester PGD2-1-glyceryl ester endocannabinoids anandamides 2AG fatty acids porcine brain isomerase moiety cannabinoids cbs synthetic 35.810524861878
10192 Prostaglandin D2 serinol amide - >98% 2004-05-13 38.065237569061 prostaglandin-d2-serinol-amide PGD2-SA PGD2 vasodilation prostaglandins brain sleep platelets aggregation anandamides serinols amides cannabinoids AEA 38.065237569061
10140 Prostaglandin E2-1-glyceryl ester 37497-47-5 >98% (as a 85:15 mixture of the 1- and 2-glyceryl esters) 50.722817679558 prostaglandin-e2-1-glyceryl-ester PGE2-1-glyceryl ester Prostaglandins PGE2-1-GE esters 2-AG 2-arachidonyl-glycerol metabolites COX-2 PGHS-2 cycloxygenases synthases PGE2-2-GE COX2 PGHS2 cannabinoids cbs synthetic 50.722817679558
14012 Prostaglandin E2 Ethanolamide Exclusive 194935-38-1 >98% ✓ 43.989917127072 prostaglandin-e2-ethanolamide PGE2-EA; Dinoprostone Ethanolamide; Prostamide E2 anandamides ethanolamides cannabinoids PGE2 prostaglandins AEA analogs neurochemistry neuroscience ethanolamines prostamides 43.989917127072
10193 Prostaglandin E2 serinol amide Exclusive - ≥98% ✓ 2004-03-03 36.179234411997 prostaglandin-e2-serinol-amide PGE2-SA PGE2SA cannabinoids agonists CB1 receptors analogs 2-glyceryl neurochemistry neuroscience 36.179234411997
10139 Prostaglandin F2α-1-glyceryl ester 43042-79-1 >98% (as a 9:1 mixture of the 2- and 1-glyceryl esters) 17.860110497238 prostaglandin-f2-1-glyceryl-ester PGF2α-1-glyceryl ester Prostaglandins PGF2alpha-1-GE PGF2.alpha.-1-GE esters 2-AG 2-arachidonoyl-glycerol COX-2 metabolites cyclooxygenases PGHS-2 synthases PGHS2 COX2 PGF2alpha-2-GE PGF2.alpha.-2-GE PGFa-2-GE PGF2a-1-GE cannabinoids cbs synthetic 17.860110497238
10194 Prostaglandin F2α serinol amide - >98% 2004-02-23 14.588425414364 prostaglandin-f2-serinol-amide PGF2α-SA PGF2alphaSA PGF2.alpha.SA PGF2alpha-SA PGF2.alpha.-SA cannabinoids agonists CB1 recptors analogs 2-glyceryl esters amides neuroscience 14.588425414364
10004281 R-1 Methanandamide Phosphate - >98% 2004-08-20 21.225856353591 r-1-methanandamide-phosphate R-1MAP; (R)-(+)-Arachidonyl-1'-Hydroxy-2'-Propylamide Phosphate endocannabinoids neurotransmitters ligands AEA lipids CB1 CB2 receptors anandamides analogs agonists phosphates LPA lysophatidic acids neurochemistry neuroscience R1 cannabinoids cbs synthetic 21.225856353591
10645 RCS-4 - ≥98% 2010-11-24 116.736971034073 rcs-4 cannabinoids receptors JWHs 018 CB1 CB2 cannabimimetics forensics CBs neurochemistry cannabinoids cbs synthetic 116.736971034073
10865 RCS-4 2-methoxy isomer Exclusive - ≥98% ✓ 2011-06-15 48.632737799022 rcs-4-2-methoxy-isomer synthetic cannabinoids forensics receptors herbal spices incense JWH 250 JWH-250 JWH250 RCS4 RCS 4 analogs CB1 CB2 cannabimimetic indoles CBs 48.632737799022
10866 RCS-4 3-methoxy isomer Exclusive - ≥98% ✓ 2011-06-15 45.077700937744 rcs-4-3-methoxy-isomer cannabinoids receptors JWH 018 CB1 CB2 CBs cannabimimetics forensics synthetic bath salts JWH-018 JWH018 45.077700937744
10798 RCS-4-C4 homolog Exclusive - ≥98% ✓ 2011-04-21 42.903849575109 rcs-4-c4-homolog BTM-4; SR-19; OBT-199; E-4 cannabinoids cannabimimetic metabolites CB1 CB2 receptors agonists spice forensics synthetics smoking urinary urine serum JWH018 JWH 018 JWH-018 JWH18 BTM4 BTM 4 E4 E 4 OBT199 OBT 199 SR19 SR 19 42.903849575109
10513 RCS-4-d9 - ≥99% deuterated product 2011-09-12 34.954514656230 rcs-4-d9 cannabinoids receptors JWHs 018 CB1 CB2 cannabimimetics forensics sciences CBs neurochemistry synthetic standards deuterated deuterium mass spectrometry LC-MS LC/MS GC-MS GC/MS MS 34.954514656230
10936 RCS-4 N-(4-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-29 37.546372595367 rcs-4-n-4-hydroxypentyl-metabolite cannabinoids cannabimimetics metabolites CB1 CB2 CBs receptors agonists spices synthetic smoking urinary urine RCS4 RCS 4 JWHs glucuroconjugate forensics sciences neuroscience 37.546372595367
10937 RCS-4 N-(5-carboxypentyl) metabolite - ≥98% 2011-06-28 41.962303867402 rcs-4-n-5-carboxypentyl-metabolite RCS4 RCS 4 forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics 41.962303867402
10935 RCS-4 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-06-17 48.680381189597 rcs-4-n-5-hydroxypentyl-metabolite cannabinoids cannabimimetic metabolites CB1 CB2 CBs receptors agonists spices forensics synthetic smoking urinary urine RCS4 RCS 4 JWHs glucuroconjugate forensics sciences neuroscience 48.680381189597
10636 RCS-8 - ≥98% 2010-11-02 98.138615251861 rcs-8 SR-18 cannabinoids receptors JWH 250 CB1 CB2 cannabimimetics forensics cannabinoids cbs synthetic Rabbit Aorta Contracting Substance A2 Thromboxane Thromboxane A2 98.138615251861
10864 RCS-8 3-methoxy isomer Exclusive - ≥98% ✓ 2011-07-13 27.721609116022 rcs-8-3-methoxy-isomer RCS 8 RCS8 isomers CBs cannabinoids forensics sciences RCS-4 RCS4 cannabimimetics CB1 CB2 receptors agonists spices synthetics extracts cannabis herbal blends 27.721609116022
10863 RCS-8 4-methoxy isomer Exclusive - ≥95% ✓ 2011-07-13 34.160325966851 rcs-8-4-methoxy-isomer RCS8 RCS 8 isomers forensics sciences RCS4 RCS-4 CBs cannabinoids cannabimimetics CB1 CB2 receptors agonists spices synthetics 34.160325966851
9000484 Rimonabant 168273-06-1 ≥98% 2009-06-17 74.152900552486 rimonabant SR141716 SR 141716A SR141716A CB1 inverse agonists anti-obesity immunomodulation anti-proliferation appetite suppressants receptors weight control medication cannabinoids anti-proliferative immunodulatory cbs sythetic 74.152900552486
10899 (R)-(−)-JWH 073 N-(3-hydroxybutyl) metabolite - ≥98% 2011-11-18 17.885706179660 -r-jwh-073-n-3-hydroxybutyl-metabolite cannabinoids metabolites cannabimimetics forensics herbal blends spices adulterant enantiomer liver microsomes glucuronidate urine CBs JWHs JWH073 JWH-073 JWH 73 JWH73 JWH-73 17.885706179660
10898 (S)-(+)-JWH 073 N-(3-hydroxybutyl) metabolite - ≥98% 2011-11-18 17.439573582975 -s-jwh-073-n-3-hydroxybutyl-metabolite cannabinoids metabolites cannabimimetic forensics herbal blends spices CBs JWH073 JWH-073 JWH 73 JWH73 JWH-73 JWHs enantiomer liver microsomes glucuronidate urine 17.439573582975
10009226 (±)-SLV 319 Exclusive 362519-49-1 ≥98% ✓ 2007-01-16 25.542371440714 -slv-319 CB1 CB2 Receptors Cannabinoids Antagonists Inflammations inflammatory neurochemistry lipophilic ligands cannabinoids cbs synthetic 25.542371440714
9000491 SR 144528 192703-06-3 ≥98% 2009-08-05 72.405013812154 sr-144528 antagonist CB1 CB2 cannabinoids receptors inverse agonist inflammation leukocytes CP 55940 CP55940 55,940 CP55,940 pain initiation suppression immune activation sr144528 CBs synthetic 72.405013812154
11564 STS-135 Exclusive New 1354631-26-7 ≥98% ✓ 2012-03-28 242.522906592621 sts-135 N-adamantyl-1-fluoropentylindole-3-Carboxamide cannabinoids CBs herbals spices forensics CB1 CB2 receptors agonists designer drugs STS 135 STS135 fluoropentylindole AM2201 AM-2201 AM 2201 synthetics peripheral 242.522906592621
13830 Synthetic Cannabinoid HPLC Mixture I - ≥95% for each compound 2010-05-13 40.045118847375 synthetic-cannabinoid-hplc-mixture-i cannabinoids CBs endocannabinoids cannabidiols CP-47,497 cp 47,497 47,497-c8-homolog CP-47,497-C8 homolog analog CP-55,940 cp47,497 cp55,940 cp 55,940 HU-331 HU331 HU 331 HU308 HU 308 HU-308 JWH-015 jwh015 jwh 015 jwh 018 jwh018JWH-018 JWH-200 jwh200 jwh 200 jwh 250 jwh250 JWH-019 Win-55212-2 Jwh-250 win 55212-2 win55212 2 synthetic spices mixes synthetic 40.045118847375
13850 Synthetic Cannabinoid HPLC Mixture II - ≥95% for each compound 2010-12-21 44.388457144890 synthetic-cannabinoid-hplc-mixture-ii cannabinoids CBs synthetics mixtures receptors agonists synthetic 44.388457144890
11335 Synthetic Cannabinoid HPLC Mixture III New - ≥95% for each compound 2012-03-20 75.250490689850 synthetic-cannabinoid-hplc-mixture-iii cannabinoids CBs synthetics mixtures receptors agonists JWHs AMs RCS 75.250490689850
11336 Synthetic Cannabinoid HPLC Mixture IV New - ≥95% for each compound 2012-05-03 100.564303915699 synthetic-cannabinoid-hplc-mixture-iv cannabinoids CBs synthetics mixtures receptors agonists JWHs AMs 100.564303915699
11337 Synthetic Cannabinoid HPLC Mixture V (AM Series) New - ≥95% for each compound 2012-02-02 40.873690480371 synthetic-cannabinoid-hplc-mixture-v-am-series AM series AM-2201 AM-1220 AM-630 AM-1241 AM-694 AM-2233 AM2201 AM1220 AM630 AM1241 AM694 CBs cannbinoids mixtures AM2233 40.873690480371
11502 UR-144 New 1199943-44-6 ≥98% 2012-04-02 409.791972624799 ur-144 KM-X1 cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetics UR144 UR 144 peripheral central KMX-1 KMX 1 KM X1 409.791972624799
13261 URB447 Exclusive 1132922-57-6 ≥98% ✓ 2009-06-18 35.040220994475 urb447 CB1 CB2 cannabinoids antagonists obesity SR 141716A SR141716A rimonabant blood brains barrier URB appetite suppressant receptors URB-447 URB blocking peptides 447 cannabinoids cbs synthetic 35.040220994475
10046 URB597 546141-08-6 >98% 47.222456052235 urb597 FAAH fatty acid amide hydrolases inhibitors URB-597 anandamides lipids inhibition selective selectivity AEA inhibits hydrolysis hydrolyze arachidonoyl cannabinoids ethanolamides neuroscience neurochemistry 47.222456052235
10007457 URB602 565460-15-3 >98% 2005-09-06 40.775469613259 urb602 monoglycerol lipase MGL inhibition inhibits inhibitors rat brain enzymes enhanced stress-induced analgesia novel drugs pain stress management CNS central nervous system monoacylglycerol neuroscience neurochemistry cannabinoids cbs synthetic 40.775469613259
10007691 URB754 86672-58-4 >98% 2005-11-04 33.701977900552 urb754 neurochemistry neuroscience 2-AG 2-archidonoyl glyerol MGL monoacylglycerol lipase monoglyceride lipase endocannabinoids FAAH fatty acid amide hydrolase inhibitors inhibition inhibits monoglycerol MAGL neurochemistry cannabinoids 33.701977900552
10674 URB937 Exclusive 1357160-72-5 ≥95% ✓ 2011-03-08 15.000916206261 urb937 FAAH anandamide AEA inhibitors peripheral pain Cannabinoids 15.000916206261
9001204 WIN 54461 Exclusive New 166599-63-9 ≥98% ✓ 2012-04-11 92.324171225580 win-54461 6-Bromopravadoline cannabinoids CBs receptors CB1 CB2 antagonists neuroscience forensics WIN-54461 WIN54461 mimetics WIN 55212-2 WIN 552122 WIN-55212-2 WIN55212-2 aminoalikylindoles WIN 54,461 10009023 10763 vas deferens inhibition inhibits inhibitors 92.324171225580
10009023 (+)WIN 55212-2 (mesylate) 131543-23-2 ≥98% 2006-10-05 59.227790192713 -win-55212-2-mesylate WIN-2 agonists cannabinoids CB1 CB2 neurons rat glutamates SR141716A IP3 Xestospongin C 55212-3 WIN-3 inflammatory neuropeptides CGRP trigeminal neurochemistry ganglions TG exocytosis WIN55,212-2 endocrinology WIN55212-2 cannabinoids cbs synthetic 59.227790192713
10736 (±)WIN 55212 (mesylate) New 137795-17-6 ≥98% 2012-01-11 46.514430542014 -win-55212-mesylate cannabinoids CB1 CB2 receptors pain neuroscience agonists antagonists aminoalkylindole CBs enantiomers (+)WIN 55212-2 (-)WIN 55215-3 SR144528 SR-144528 SR 144528 racemic mesylate central peripheral 46.514430542014
11565 XLR11 Exclusive New 1364933-54-9 ≥98% ✓ 2012-04-10 391.634701678218 xlr11 cannabinoids CBs cannabimimetic receptors CB1 CB2 designer drugs forensics neuroscience XLR-11 XLR 11 central peripheral 391.634701678218
11688 XLR11 N-(4-pentenyl) analog Exclusive New - ≥98% ✓ 2012-05-08 299.757058969709 xlr11-n-4-pentenyl-analog UR-144 N-(4-pentenyl) analog cannabinoids CBs CB1 CB2 forensics spices herbals neuroscience XLR-11 XLR 11 AM2201 MAM2201 AM 2201 AM-2201 MAM 2201 MAM-2201 analogs 11565 central peripheral receptors K2 UR144 UR 144 UR-144 pentenyl analog 10707 9001219 299.757058969709
90215 α-Linolenoyl Ethanolamide Exclusive 57086-93-8 >98% ✓ 9.920122336227 -linolenoyl-ethanolamide cannabinoids neurotransmitters ethanolamides fatty acids CB alpha-linolenoyl .alpha.-linolenoyl cannabinergic neurochemistry neuroscience ethanolamines, cbs, synthetic 9.920122336227
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