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Join us! · InformexUSA 2012 · New Orleans, Louisiana · February 14-17, 2012 · Booth 2514

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 6.273825966850 -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 6.273825966850
10009897 (−)-11-nor-9-carboxy-Δ9-THC (solution) 56354-06-4 ≥98% 2010-11-11 6.639502762431 -11-nor-9-carboxy-9-thc-solution THC metabolites Delta9-THC Δ9-THC tetrahydrocannabinols marijuana cannabinoids cbs synthetic 10915 6.639502762431
10010132 15-deoxy-Δ12,14-Prostaglandin J2-2-glycerol ester - ≥98% (isomer mixture) 2008-06-09 26.555457335788 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 26.555457335788
14810 17-phenyl trinor Prostaglandin E2 38315-43-4 >98% 56.688241252302 17-phenyl-trinor-prostaglandin-e2 17-phenyl trinor PGE2 agonists EP1 EP3 prostaglandins receptors 17-phenyl-trinor-PGE2 56.688241252302
10004238 17-phenyl trinor Prostaglandin E2 serinol amide - ≥95% 2004-05-13 117.110243093922 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 117.110243093922
10004237 17-phenyl trinor Prostaglandin F2α serinol amide - >98% 2004-03-15 7.416194751381 17-phenyl-trinor-prostaglandin-f2-serinol-amide 17-phenyl trinor PGF2α-SA; 17-phenyl trinor PGF2α serinol amide; Bimatoprost serinol amide analogs agonists receptors 17-phenyl-PGF2.alpha.SA 17-phenyl-PGF2alphaSA 17-phenyl-PGF2a-SA prostaglandins cannabinoids CBs synthetic 7.416194751381
362152 1-Arachidonoyl Glycerol-d5 - ≥99% deuterated product 29.892113259668 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 29.892113259668
10008602 20-HETE Ethanolamide - ≥98% 2006-09-26 32.682062615101 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 32.682062615101
10009962 2-(14,15-Epoxyeicosatrienoyl) Glycerol 848667-56-1 ≥95% 2008-04-03 28.374088397789 2-14-15-epoxyeicosatrienoyl-glycerol 2-14,15-EG 2-AG CYP450 metabolism mitogens cancers kidneys endocannabinoids cannabinoids cbs synthetic 28.374088397789
362162 2-Arachidonoyl Glycerol-d5 - ≥99% deuterated product 46.147099447513 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 46.147099447513
362160 2-Arachidonoyl Glycerol-d8 - ≥99% deuterated product 71.042030386740 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 71.042030386740
10918 (±)3-epi CP 47,497-C8-homolog - ≥98% 2011-05-06 12.267457068203 -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 12.267457068203
13802 (±)3-epi CP 47,497-C8-homolog (solution) Exclusive - ≥98% ✓ 2010-08-04 11.371533840622 -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 11.371533840622
13140 4-(n-nonyl) Benzeneboronic Acid 256383-45-6 ≥98% 2009-11-04 6.668687845304 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 6.668687845304
11093 4-Quinolone-3-Carboxamide Derivative New 1314230-69-7 ≥98% 2012-01-30 128.388330263966 4-quinolone-3-carboxamide-derivative CB1 CB2 cannabinoid CBs central peripheral receptors inverse agonists antinociception AM630 analgesic pain osteoporosis synthetic ligands mice analgesic AM 630 AM-630 128.388330263966
13803 (±)5-epi CP 55,940 - ≥98% 2010-08-04 7.455193370166 -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 7.455193370166
10005764 8-iso Prostaglandin F2α Ethanolamide - >98% 2004-09-24 17.166390423573 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 17.166390423573
10005223 AM1172 251908-92-6 >98% 2004-09-01 25.692268262737 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 25.692268262737
9001055 AM1220 Exclusive New 137642-54-7 ≥98% ✓ 2011-10-11 118.380461040369 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 118.380461040369
10010118 AM1241 444912-48-5 >97% 2007-08-29 104.824301021262 am1241 CB1 CB2 cannabinoids receptors agonists antagonists antinociception AM630 AM251 AM-1241 AM 1241 cannabinoids cbs synthetic 104.824301021262
11282 AM1248 Exclusive New 335160-66-2 ≥98% ✓ 2012-02-06 128.785932020974 am1248 CBs cannabinoids synthetic agonist AM-1248 AMs 1248 forensic sciences receptors CB1 CB2 1-pentyl-3-(1-adamantoyl)indole AM679 AM-679 679 128.785932020974
10707 AM2201 Exclusive 335161-24-5 ≥98% ✓ 2011-03-07 122.875871207581 am2201 cannabinoids CB1 CB2 receptors pain forensic sciences CBs AM-2201 AM 2201 122.875871207581
10862 AM2201 2'-naphthyl isomer Exclusive - ≥98% ✓ 2011-07-06 68.319292234126 am2201-2-naphthyl-isomer AM-2201 AM 2201 cannabinoids CBs isomers AMs forensics sciences cannabimimetics CB1 CB2 receptors agonists spices synthetics 68.319292234126
11193 AM2201 7-hydroxyindole metabolite New - ≥98% 2012-01-16 119.790823986937 am2201-7-hydroxyindole-metabolite forensics sciences AM-2201 AM 2201 isomers cannabinoids receptors pain CBs CB1 CB2 metabolites urinary urine metabolism synthetic central peripheral 119.790823986937
10706 AM2201-d5 Exclusive - ≥99% deuterated product ✓ 2011-05-16 41.327683482825 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 41.327683482825
9001031 AM2201 N-(2-fluoropentyl) isomer New - ≥95% 2011-12-15 125.960721783419 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 125.960721783419
9001030 AM2201 N-(3-fluoropentyl) isomer New - ≥98% 2011-11-22 95.664221144848 am2201-n-3-fluoropentyl-isomer forensics AM-2201 AM 2201 isomers cannabinoids CBs receptors pain CBs CB1 CB2 95.664221144848
9001029 AM2201 N-(4-fluoropentyl) isomer Exclusive - ≥98% ✓ 2011-08-11 65.690699556963 am2201-n-4-fluoropentyl-isomer forensics sciences AM-2201 AM 2201 isomers cannabinoids receptors pain CBs CB1 CB2 central peripheral 65.690699556963
10203 AM2201 N-(4-hydroxypentyl) metabolite Exclusive New - ≥98% ✓ 2011-10-11 105.795305348014 am2201-n-4-hydroxypentyl-metabolite AM-2201 AM 2201 cannabinoids cannabimimetic metabolites CB1 CB2 CBS receptors forensics synthetics smoking urinary urine potent synthetic 105.795305348014
11008 AM2233 New 444912-55-4 ≥98% 2011-10-24 100.230828316970 am2233 769958-75-0 forensic science cannabinoid receptors CB1 agonists WIN 55,212-2 WIN 55212-2 radioligands neuroscience 100.230828316970
71670 AM251 183232-66-8 >98% 76.381213014119 am251 cannabinoids receptors antagonists CB1 analogs selective SR-141716-A AM-251 SR141716A neuroscience neurochemistry endocrinology 76.381213014119
13452 AM3102 Exclusive 213182-22-0 ≥98% ✓ 2009-08-11 45.108392879067 am3102 KDS-5104 OEA PPARs PPARα KDS5104 antiobesity anti-obesity CB1 CB2 endocannabinoids obesity cannabinoids inhibitors agonists receptors cbs synthetic 45.108392879067
10006974 AM630 164178-33-0 ≥98% 2009-02-09 47.163132289748 am630 Iodopravadoline neurochemistry neuroscience cannabinoids CB1 CB2 antagonist inverse agonist antinociception pain receptors 47.163132289748
10567 AM694 Exclusive 335161-03-0 ≥95% ✓ 2011-01-31 55.781724575096 am694 cannabinoids CB1 CB2 receptors pain JWH neuroscience AM-694 AM 694 55.781724575096
10870 AM694 3-iodo isomer Exclusive New - ≥98% ✓ 2011-08-31 55.513620654394 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 55.513620654394
10869 AM694 4-iodo isomer Exclusive - ≥97% ✓ 2011-06-21 29.220392980301 am694-4-iodo-isomer cannabinoids CBs cannabimimetics CB1 CB2 pain spices forensics synthetic receptors agonists AM-694 AM 694 analogs neuroscience 29.220392980301
10008617 Arachidonic Acid Leelamide - ≥95% 2006-09-27 13.333687845304 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 13.333687845304
10007904 Arachidonoyl-1-thio-Glycerol Exclusive - >98% ✓ 2006-01-24 18.352375690608 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 18.352375690608
10011178 Arachidonoyl Ethanolamide-d4 946524-40-9 ≥99% deuterated product 2008-03-04 35.926298342541 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 35.926298342541
10180 Arachidonoyl Ethanolamide Phosphate 183323-26-4 >98% 2004-08-19 15.640524861879 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 15.640524861879
62170 Arachidonoyl Serinol 183718-70-9 >98% 32.943646408840 arachidonoyl-serinol endocannabinoids anandamides 2AG CB1 receptors neurochemistry neuroscience cannabinoids cbs synthetic 32.943646408840
13823 AX 048 Exclusive 873079-69-7 ≥98% ✓ 2010-09-15 9.193425414365 ax-048 Inflammation antihyperalgesia cPLA2 phospholipases inhibitors inhibition inhibits AX048 AX-048 signaling signalling group IVA PLA2 cannabinoids cbs synthetic Acids Octanoic Octanoic Acids 9.193425414365
10506 Bio-active Lipid I Screening Library (96-Well) - 2010-06-15 44.241464088397 bio-active-lipid-i-screening-library-96-well vasoconstriction bronchoconstriction prostaglandins endocrinology prostaglandins HTS high thoroughput screening cannabinoids cbs synthetic 44.241464088397
90080 Cannabidiol 13956-29-1 >99% 26.647332280978 cannabidiol CBD delta9-THC .DELTA.9-THC delta9THC .DELTA.9THC marijuana neuroprotective tetrahydrocannabidiol d9-THC d9THC neurochemistry neuroscience synthetic cbs cannabinoids 26.647332280978
13285 Cannabidiol dimethyl ether 1242-67-7 ≥98% 2009-05-19 12.557320441989 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 12.557320441989
90081 Cannabidiol (solution) 13956-29-1 ≥99% 2011-03-03 33.602882973380 cannabidiol-solution CBD delta9-THC .DELTA.9-THC delta9THC .DELTA.9THC marijuana neuroprotective tetrahydrocannabidiol d9-THC d9THC neurochemistry neuroscience synthetic cbs cannabinoids 33.602882973380
10508 Cannabinoid Agonist Screening Library (96-Well) - 2011-05-05 3.314917127072 cannabinoid-agonist-screening-library-96-well plates screening cannabinoids CBs libraries foresnics JWHs JWH-108 JWH-200 HU 210 CPs 3.314917127072
71652 CAY10401 288862-89-5 >98% 2005-02-02 8.948825046040 cay10401 FAAH inhibitors analgesics fatty acids amides hydrolases inhibits inhibition hydrolysis hydrolyze CAY-10401 inactivation anandamides AEA arachidonoyl ethanolamides neuroscience neurochemistry cannabinoids cbs synthetic 8.948825046040
10009523 CAY10429-d3 - ≥99% deuterated product 2007-10-02 1.414364640884 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 1.414364640884
10008669 CAY10508 878533-35-8 >98% 2006-08-04 27.353314917127 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 27.353314917127
10010398 CB-13 432047-72-8 ≥98% 2009-06-30 30.332404939876 cb-13 CRA-13 cannabinoids CB1 CB2 central peripheral receptors agonists pains hyperalgesia blocks blocking CB13 CB 13 CRA13 CRA 13 30.332404939876
10006590 CB1 Receptor (C-Term) Polyclonal Antibody - 2005-05-10 58.365460405156 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 58.365460405156
10010116 CB-25 Exclusive 869376-63-6 >98% ✓ 2007-10-25 16.706774861878 cb-25 cannabinoids ligands receptors CB1 CB2 THC anandamides AEA inverse agonists cannabinoids cbs synthetic 16.706774861878
10010117 CB-52 Exclusive 869376-90-9 ≥98% ✓ 2007-10-25 16.798142265193 cb-52 cannabinoids ligands receptors CB1 CB2 THCs anandamides AEAs partial agonists neutral antagonists cannabinoids cbs synthetic 16.798142265193
13289 CB-86 Exclusive 1150586-64-3 ≥98% ✓ 2010-05-03 17.649021310181 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 17.649021310181
10917 (−)-CP 47, 497 114753-51-4 ≥98% 2011-05-05 14.108511156878 -cp-47-497 cannabinoids analgesia CB1 hypothermia motor deppressant anticonvulsant Δ9-THC analogs activity hypothermic effects cannabinoids cbs synthetic 13218 14.108511156878
10910 (+)-CP 47,497 134308-14-8 ≥98% 2011-05-05 13.627848173453 -cp-47-497 cannabinoid analgesia analgesic CB1 hypothermia motor depressant anticonvulsant Δ9-THC CBs analogs cbs synthetic cannabinoids 13.627848173453
10913 (±)-CP 47,497 70434-82-1 ≥98% 2011-05-05 29.260334883041 -cp-47-497 receptors agonist CB1 potent cannabinoid DELTA9-THC Δ9-THC CP47,497 CP-47,497 CP47497 CP-47497 cannabinoids cbs synthetic 16851 29.260334883041
9000774 (±)-CP 47,497 C-7-hydroxy metabolite New - ≥95% 2011-11-04 147.044459984460 -cp-47-497-c-7-hydroxy-metabolite cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic metabolites herbal adulterant CP47,497 CP-47,497 147.044459984460
10908 (±)-CP 47,497-C8-homolog Exclusive 70434-92-3 ≥98% ✓ 2011-05-06 33.211843073581 -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 33.211843073581
9000773 CP 47,497-C8-homolog C-8-hydroxy metabolite New - ≥98% 2012-01-03 78.095627948632 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 78.095627948632
10686 (±)-CP 47,497-C8-homolog-d7 (solution) Exclusive - ≥99% deuterated forms (d1-d7) ✓ 2011-03-14 21.771818898971 -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 21.771818898971
13216 (±)-CP 47,497-C8-homolog (solution) Exclusive 70434-92-3 ≥98% ✓ 2009-04-23 43.502412536909 -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 43.502412536909
10687 (±)-CP 47,497-d11 (solution) Exclusive - ≥99% deuterated forms (d1-d11) ✓ 2011-02-16 23.337757971923 -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 23.337757971923
10889 CP 47,497-para-quinone analog Exclusive - ≥90% ✓ 2011-07-13 13.459269521965 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 13.459269521965
13218 (−)-CP 47,497 (solution) 114753-51-4 ≥98% 2009-04-13 16.635470743702 -cp-47-497-solution cannabinoids analgesia CB1 hypothermia motor deppressant anticonvulsant Δ9-THC analogs activity hypothermic effects cannabinoids cbs synthetic 10917 16.635470743702
13219 (+)-CP 47,497 (solution) 134308-14-8 ≥98% 2009-04-13 17.680171898900 -cp-47-497-solution cannabinoid analgesia analgesic CB1 hypothermia motor depressant anticonvulsant Δ9-THC CBs analogs cbs synthetic cannabinoids 10910 17.680171898900
16851 (±)-CP 47,497 (solution) 70434-82-1 ≥98% 2008-12-10 40.643750448281 -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 40.643750448281
90084 (−)-CP 55,940 83002-04-4 ≥98% 2007-01-15 30.013067923302 -cp-55-940 CP 55940 CP-55940 CP-55,940 agonists cannabinoids CB1 CB2 THC receptors endocrinology cp55940 cp55,940 neurochemistry cbs synthetic 30.013067923302
13608 (+)-CP 55,940 Exclusive - ≥98% ✓ 2010-05-20 16.533217169570 -cp-55-940 Δ9-THC cannabinoids CB1 CB2 pain analgesic cannabinoids cbs synthetic 16.533217169570
13241 (±)-CP 55,940 Exclusive 83003-12-7 ≥98% ✓ 2009-05-20 24.597446286065 -cp-55-940 cannabinoids analgetic pain THC thermal mechanical chemicals receptors CB1 cannabimimetic potent non-selective CP55940 CP-55940 cbs synthetic 24.597446286065
10007534 Docosahexaenoyl Ethanolamide Exclusive 162758-94-3 ≥98% ✓ 2006-02-17 22.962016574585 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 22.962016574585
10964 Eicosapentaenoyl Ethanolamide 109001-03-8 ≥98% 2011-06-22 40.873259668508 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 40.873259668508
10919 (±)-epi CP 47, 497 - ≥98% 2011-05-05 13.604473642789 -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 13.604473642789
13801 (±)-epi CP 47,497 (solution) Exclusive - ≥98% ✓ 2010-08-04 11.620194114805 -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 11.620194114805
10004236 Fluprostenol serinol amide - ≥98% 2004-09-23 25.495878453039 fluprostenol-serinol-amide Flu-SA PGF2.alpha. PGF2alpha analogs agonists prostaglandins receptors amides cannabinoids CB1 CBs synthetic 25.495878453039
10011357 Glycerophospho-N-Oleoyl Ethanolamine Exclusive 201738-24-1 ≥98% ✓ 2009-02-20 22.960773480663 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 22.960773480663
10011356 Glycerophospho-N-Palmitoyl Ethanolamine Exclusive 100575-09-5 ≥98% ✓ 2009-03-12 11.982209944751 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 11.982209944751
10224 GPR55 Polyclonal Antibody - 2010-01-19 38.641258879242 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 38.641258879242
10010372 GW 842166X 666260-75-9 ≥98% 2008-05-23 35.737209944751 gw-842166x inflammatory pain arthritis neuropathic hyperalgesia CB2 cannabinoids agonists anandamide receptors neurochemistry cannabinoids cbs synthetic 35.737209944751
10011038 Hemopressin - 2009-08-13 32.880710339384 hemopressin peptides antagonist inhibitors inhibits inhibition hypertension binding asoactive vasoactive cannabinoids cbs synthetic 32.880710339384
90082 HU-210 112830-95-2 >98% 44.104514848065 hu-210 agonists analogs d9-THC marijuana CB1 CB2 receptors cannabinoids HU210 .DELTA.9-THC delta9-THC neuroscience neurochemistry endocrinology cannabinoids cbs synthetic 44.104514848065
90083 HU-210 (solution) 112830-95-2 ≥98% 2011-03-03 26.336929755327 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 26.336929755327
10005673 HU-331 137252-25-6 ≥95% 2005-09-09 28.665938203397 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 28.665938203397
10266 JWH 007 Exclusive 155471-10-6 ≥98% ✓ 2011-02-23 39.806735761424 jwh-007 agonists cannabinoids receptors CB1 CB2 Δ9-THC pain antinociception hypothermia catalepsy JWHs CBs JWH-007 JWH007 JWH-7 JWH 7 JWH7 39.806735761424
10486 JWH 007-d9 - ≥99% deuterated product 2010-10-11 42.265883416430 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 42.265883416430
9001058 JWH 011 Exclusive New 155471-13-9 ≥98% ✓ 2011-09-06 35.616664171055 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 35.616664171055
10009018 JWH 015 155471-08-2 ≥98% 2006-10-05 71.726170738024 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 71.726170738024
10660 JWH 015-d7 Exclusive - ≥99% deuterated product ✓ 2011-02-21 49.700773480663 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 49.700773480663
10849 JWH 016 Exclusive 155471-09-3 ≥95% ✓ 2011-07-13 46.194218095568 jwh-016 JWH016 JWH-016 cannabinoids CBs receptors isomers forensics sciences JWHs agonists cannabimimetics CB1 CB2 receptors agonists spices synthetics 46.194218095568
10900 JWH 018 209414-07-3 ≥98% 2011-05-05 39.860919038187 jwh-018 cannabinoids CB1 CB2 agonists selective receptors WIN 55212-2 JWH-018 JWH018 cbs synthetic JWH 18 JWH-018 JWH18 JWH-18 13169 39.860919038187
9000844 JWH 018 2-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-10-26 31.132379618776 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 31.132379618776
10711 JWH 018 2-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated product ✓ 2011-02-25 24.113084443524 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 24.113084443524
9001004 JWH 018 2'-naphthyl isomer Exclusive 1131605-25-8 ≥98% ✓ 2011-06-20 41.582030283835 jwh-018-2-naphthyl-isomer JWH018 JWH-018 CBs cannabinoids forensics sciences cannabimimetic CB1 CB2 receptors agonist spices synthetic 41.582030283835
9001006 JWH 018 2'-naphthyl-N-(1,2-dimethylpropyl) isomer Exclusive New - ≥98% ✓ 2011-10-11 22.875346781817 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 22.875346781817
9001009 JWH 018 2'-naphthyl-N-(1-methylbutyl) isomer - ≥98% 2011-06-20 25.662569449162 jwh-018-2-naphthyl-n-1-methylbutyl-isomer JWH018 JWH-018 CBs cannabinoids forensics sciences cannabimimetic CB1 CB2 receptor agonist spices synthetic 25.662569449162
9001008 JWH 018 2'-naphthyl-N-(2,2-dimethylpropyl) isomer - ≥98% 2011-06-28 31.105322736730 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 31.105322736730
9001010 JWH 018 2'-naphthyl-N-(2-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-13 27.775441093980 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 27.775441093980
9001005 JWH 018 2'-naphthyl-N-(3-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-13 26.411057887728 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 26.411057887728
9000851 JWH 018 4-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 46.814097970685 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 46.814097970685
10712 JWH 018 4-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated product ✓ 2011-02-25 33.195926243109 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 33.195926243109
9000852 JWH 018 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 69.338314927368 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 69.338314927368
10713 JWH 018 5-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated product ✓ 2011-03-11 27.502696454894 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 27.502696454894
9000853 JWH 018 6-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 42.598628357426 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 42.598628357426
10714 JWH 018 6-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated product ✓ 2011-03-25 47.737945073679 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 47.737945073679
10697 JWH 018 6-methoxyindole analog Exclusive - ≥98% ✓ 2011-02-15 30.978954958867 jwh-018-6-methoxyindole-analog analogs metabolites cannabinoids receptors agonists CBs JWH-018 JWH018 JWH18 JWH-18 JWH 18 30.978954958867
9000854 JWH 018 7-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 37.179710050102 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 37.179710050102
10715 JWH 018 7-hydroxyindole metabolite-d9 Exclusive - ≥99% deuterated product ✓ 2011-07-26 29.253143271526 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 29.253143271526
9000799 JWH 018 adamantyl analog Exclusive - ≥97% ✓ 2011-07-18 40.803083811230 jwh-018-adamantyl-analog AB-001 JWH 018 JWH-018 JWHs analogs forensics sciences cannabinoids CBs receptors WIN 55,212-2 CB1 CB2 cannabimimetics 40.803083811230
13824 JWH 018-d9 (solution) - ≥99% deuterated product 2010-06-21 54.097431772776 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 54.097431772776
9001000 JWH 018 N-(1,1-dimethylpropyl) isomer New - ≥98% 2011-11-16 37.203630991269 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 37.203630991269
9001003 JWH 018 N-(1,2-dimethylpropyl) isomer Exclusive New - ≥98% ✓ 2011-10-11 25.764946879970 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 25.764946879970
9001002 JWH 018 N-(1-methylbutyl) isomer Exclusive - ≥98% ✓ 2011-06-17 27.001535271697 jwh-018-n-1-methylbutyl-isomer JWH-018 JWH018 CBs cannasbinoids forensic sciences cannabimimetic CB1 CB2 receptors agonist spices synthetic 27.001535271697
9001001 JWH 018 N-(2,2-dimethylpropyl) isomer - ≥98% 2011-06-27 32.075737101371 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 32.075737101371
11119 (±)-JWH 018 N-(2-hydroxypentyl) metabolite New - ≥98% 2011-12-07 66.739667883151 -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 66.739667883151
10690 JWH 018 N-(2-methylbutyl) isomer Exclusive - ≥97% ✓ 2011-03-16 21.750250279686 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 21.750250279686
11118 JWH 018 N-(3-hydroxypentyl) metabolite New - ≥98% 2011-11-17 44.999861027700 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 44.999861027700
10691 JWH 018 N-(3-methylbutyl) isomer Exclusive - ≥97% ✓ 2011-02-07 25.015270666904 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 25.015270666904
11075 JWH 018 N-(4,5-epoxypentyl) analog New - ≥98% 2011-10-21 29.167137472777 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 29.167137472777
10921 (−)-JWH 018 N-(4-hydroxypentyl) metabolite New - ≥98% 2011-12-07 63.986504246787 -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 63.986504246787
10920 (+)-JWH 018 N-(4-hydroxypentyl) metabolite New - ≥98% 2011-12-07 70.342867883151 -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 70.342867883151
10796 (±)-JWH 018 N-(4-hydroxypentyl) metabolite Exclusive - ≥97% ✓ 2011-05-31 44.595594023696 -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 44.595594023696
10926 (±)-JWH 018 N-(4-hydroxypentyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-06-28 51.336977083511 -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 51.336977083511
11047 JWH 018 N-(5-bromopentyl) analog New - ≥98% 2012-01-19 136.655819724129 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 136.655819724129
10521 JWH 018 N-(5-chloropentyl) analog New - ≥95% 2012-01-17 147.981840723864 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 147.981840723864
9000855 JWH 018 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2010-09-01 111.610033422934 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 111.610033422934
10933 JWH 018 N-(5-hydroxypentyl) metabolite-d5 Exclusive - ≥99% deuterated product ✓ 2011-06-22 79.757840793639 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 79.757840793639
10958 JWH 018 N-(5-hydroxypentyl) β-D-Glucuronide Exclusive New - ≥95% ✓ 2011-12-20 107.341983086389 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 107.341983086389
9000856 JWH 018 N-pentanoic acid metabolite Exclusive - ≥95% ✓ 2010-09-01 110.132510405829 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 110.132510405829
9000867 JWH 018 N-pentanoic acid metabolite-d4 Exclusive - ≥99% deuterated product ✓ 2010-09-15 280.977045593935 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 280.977045593935
13169 JWH 018 (solution) 209414-07-3 ≥98% 2009-03-12 68.923268613605 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 68.923268613605
13633 JWH 019 209414-08-4 ≥98% 2010-01-14 50.127632658708 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 50.127632658708
9000764 JWH 019 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-06 26.981218665814 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 26.981218665814
9000765 JWH 019 N-(6-hydroxyhexyl) metabolite Exclusive New - ≥98% ✓ 2011-10-13 30.547854892471 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 30.547854892471
10850 JWH 020 Exclusive 209414-09-5 ≥98% ✓ 2011-06-02 43.933702363359 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 43.933702363359
9001056 JWH 022 Exclusive 209414-16-4 ≥98% ✓ 2011-08-09 84.562414988077 jwh-022 JWH022 JWH-022 JWH22 JWH-22 JWHs cannabinoids CBs synthetic standards forensics sciences 84.562414988077
10831 JWH 030 Exclusive New 162934-73-8 ≥98% ✓ 2011-10-11 59.469825443952 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 59.469825443952
10904 JWH 073 208987-48-8 ≥97% 2011-05-06 40.353743785596 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 40.353743785596
10633 JWH 073 2-hydroxyindole metabolite - ≥98% 2011-01-11 37.668238301845 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 37.668238301845
10716 JWH 073 2-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated product ✓ 2011-03-10 19.228790996521 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 19.228790996521
10848 JWH 073 2-methylnaphthyl analog Exclusive New - ≥98% ✓ 2011-10-11 28.319358014608 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 28.319358014608
9001014 JWH 073 2'-naphthyl isomer Exclusive - ≥97% ✓ 2011-06-13 32.233909747710 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 32.233909747710
9001016 JWH 073 2'-naphthyl-N-(1-methylpropyl) isomer - ≥98% 2011-06-28 36.495676592606 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 36.495676592606
9001015 JWH 073 2'-naphthyl-N-(2-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-21 31.124385649001 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 31.124385649001
9000861 JWH 073 4-hydroxyindole metabolite - ≥98% 2010-09-01 43.375395282530 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 43.375395282530
10717 JWH 073 4-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated product ✓ 2011-02-21 19.579435563740 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 19.579435563740
9001076 JWH 073 4-methylnaphthyl analog New - ≥98% 2011-09-06 35.278436481376 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 35.278436481376
9000862 JWH 073 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2010-09-01 37.173574988467 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 37.173574988467
10718 JWH 073 5-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated product ✓ 2011-03-11 21.566729128299 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 21.566729128299
9000863 JWH 073 6-hydroxyindole metabolite Exclusive - ≥95% ✓ 2010-09-01 33.166485782090 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 33.166485782090
10719 JWH 073 6-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated product ✓ 2011-03-11 19.228790996521 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 19.228790996521
9000864 JWH 073 7-hydroxyindole metabolite Exclusive - 98% ✓ 2010-09-01 30.644219555686 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 30.644219555686
10720 JWH 073 7-hydroxyindole metabolite-d7 Exclusive - ≥99% deuterated product ✓ 2011-07-25 25.409004024282 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 25.409004024282
9000868 JWH 073-d7 (solution) Exclusive - ≥99% deuterated product ✓ 2010-08-10 35.952230308723 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 35.952230308723
9001013 JWH 073 N-(1,1-dimethylethyl) isomer New - ≥98% 2012-01-12 119.645204472316 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 119.645204472316
9001012 JWH 073 N-(1-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-22 34.836065991837 jwh-073-n-1-methylpropyl-isomer JWH073 JWH-073 JWH73 JWH-73 forensics sciences cannabinoids CBs JWHs cannabimimetics CB1 CB2 receptors agonists spices synthetic 34.836065991837
9001011 JWH 073 N-(2-methylpropyl) isomer Exclusive - ≥98% ✓ 2011-06-21 28.791133147191 jwh-073-n-2-methylpropyl-isomer JWH-073 JWH073 JWH-73 JWH73 JWHs CBs cannabinoids forensic sciences cannabimimetic CB1 CB2 receptors agonists spices synthetic 28.791133147191
10795 (±)-JWH 073 N-(3-hydroxybutyl) metabolite Exclusive - ≥98% ✓ 2011-05-31 53.345126292079 -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 53.345126292079
10927 (±)-JWH 073 N-(3-hydroxybutyl) metabolite-d5 Exclusive - ≥99% deuterated forms (d1-d5) ✓ 2011-07-25 46.084455221335 -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 46.084455221335
9000865 JWH 073 N-(4-hydroxybutyl) metabolite Exclusive - ≥98% ✓ 2010-09-01 85.111283486231 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 85.111283486231
10934 JWH 073 N-(4-hydroxybutyl) metabolite-d5 Exclusive New - ≥99% deuterated product ✓ 2011-10-14 66.724011217090 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 66.724011217090
9000866 JWH 073 N-butanoic acid metabolite Exclusive - ≥98% ✓ 2010-09-01 94.707746633261 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 94.707746633261
9000870 JWH 073 N-butanoic acid metabolite-d5 Exclusive - ≥99% deuterated product ✓ 2010-09-20 88.435213297809 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 88.435213297809
13170 JWH 073 (solution) 208987-48-8 ≥97% 2009-03-02 44.560786731709 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 44.560786731709
10579 JWH 081 210179-46-7 ≥98% 2010-10-22 76.572986461864 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 76.572986461864
9001044 JWH 081 2-methoxynaphthyl isomer Exclusive New 824960-76-1 ≥98% ✓ 2011-08-23 75.399601443297 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 75.399601443297
9001045 JWH 081 3-methoxynaphthyl isomer New - ≥98% 2012-01-25 187.336528974017 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 187.336528974017
9001046 JWH 081 5-methoxynaphthyl isomer Exclusive New - ≥98% ✓ 2011-10-11 82.119364943219 jwh-081-5-methoxynaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic JWH-081 JWH081 JWH-18 JWH48 18 isomers 82.119364943219
9001047 JWH 081 6-methoxynaphthyl isomer New 824961-41-3 ≥98% 2012-01-19 167.038438607436 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 167.038438607436
9001048 JWH 081 7-methoxynaphthyl isomer Exclusive New 824961-61-7 ≥98% ✓ 2011-10-11 69.521328910252 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 69.521328910252
10511 JWH 081-d9 New - ≥99% deuterated product 2011-09-08 66.443078325278 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 66.443078325278
9000768 JWH 081 N-(5-hydroxypentyl) metabolite Exclusive - ≥95% ✓ 2011-08-05 95.818200155193 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 95.818200155193
10680 JWH 098 Exclusive 316189-74-9 ≥98% ✓ 2011-04-20 51.161757491380 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 51.161757491380
10591 JWH 122 619294-47-2 ≥98% 2010-12-15 86.826609729501 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 86.826609729501
9001032 JWH 122 2-methylnaphthyl isomer Exclusive New - ≥98% ✓ 2011-08-25 23.603525186488 jwh-122-2-methylnaphthyl-isomer JWH-122 JWH122 JWHs isomers forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics 23.603525186488
9001033 JWH 122 3-methylnaphthyl isomer New - ≥98% 2011-11-09 35.021365636895 jwh-122-3-methylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic synthetic herbal methyl naphthyl isomers JWH122 JWH-122 JWHs 35.021365636895
9001034 JWH 122 5-methylnaphthyl isomer New - ≥98% 2011-11-09 35.021365636895 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 35.021365636895
9001035 JWH 122 6-methylnaphthyl isomer Exclusive New - ≥95% ✓ 2011-10-11 39.803660502447 jwh-122-6-methylnaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetics herbal blends isomers JWH-122 JWH122 39.803660502447
9001036 JWH 122 7-methylnaphthyl isomer Exclusive New 824960-56-7 ≥98% ✓ 2011-10-11 33.349188957731 jwh-122-7-methylnaphthyl-isomer JWHs cannabinoids cannabimimetic CB1 CB2 CBs receptors agonists spices forensics synthetic herbal blends isomers JWH-122 JWH122 33.349188957731
9001037 JWH 122 8-methylnaphthyl isomer New - ≥98% 2011-11-30 53.893531714563 jwh-122-8-methylnaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic JWH-122 JWH122 herbalmethyl groups naphthyl rings herbal 53.893531714563
10512 JWH 122-d9 New - ≥99% deuterated product 2011-09-08 41.408151914141 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 41.408151914141
10925 JWH 122 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-06-17 50.501041928730 jwh-122-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 50.501041928730
10825 JWH 145 Exclusive New 914458-19-8 ≥95% ✓ 2011-11-10 26.667005378671 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 26.667005378671
11201 JWH 175 Exclusive New 619294-35-8 ≥98% ✓ 2012-02-09 130.536276661375 jwh-175 CBs JWH-175 JWH175 JWHs CB1 CB2 cannabinoids JWH018 JWH-018 JWH 018 receptors agonist spices synthetic 130.536276661375
10643 JWH 182 Exclusive New 824960-02-3 ≥97% ✓ 2011-10-11 53.435623815085 jwh-182 JWH-182 JWHs CB1 CB2 CBs receptors agonists pains spices forensics synthetics cannabinoids cells animals 53.435623815085
10902 JWH 200 103610-04-4 ≥98% 2011-05-05 47.054774727766 jwh-200 cannabinoids receptors agonists CB1 pain antinociception cannabinoids cbs synthetic JWH200 JWH-200 10902 47.054774727766
9000897 JWH 200 2'-naphthyl isomer Exclusive 133438-66-1 ≥98% ✓ 2011-06-20 22.689686475317 jwh-200-2-naphthyl-isomer JWH200 JWH-200 CBs cannabinoids forensics sciences cannabimimetic CB1 receptors agonist spices synthetic 22.689686475317
10744 JWH 200 4-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-04-15 36.781428004611 jwh-200-4-hydroxyindole-metabolite JWH-200 JWH200 cannabinoids receptors agonists pain antinociception CBs cannabimimetic metabolites CB1 CB2 spices forensics synthetic smoking urinary urine 36.781428004611
10745 JWH 200 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-06 25.218674674828 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 25.218674674828
10746 JWH 200 6-hydroxyindole metabolite Exclusive New - ≥98% ✓ 2011-10-11 29.421324798993 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 29.421324798993
10747 JWH 200 7-hydroxyindole metabolite New - ≥98% 2011-11-21 28.707235708190 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 28.707235708190
10903 JWH 200-d5 - ≥99% deuterated product 2011-05-06 10.563329852221 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 10.563329852221
10682 JWH 200-d5 (solution) - ≥99% deuterated product 2011-01-07 33.996941087390 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 33.996941087390
13171 JWH 200 (solution) 103610-04-4 ≥98% 2009-03-25 45.758690559580 jwh-200-solution cannabinoids receptors agonists CB1 pain antinociception cannabinoids cbs synthetic JWH200 JWH-200 10902 45.758690559580
10721 JWH 201 Exclusive 864445-47-6 ≥98% ✓ 2011-02-24 77.624510665918 jwh-201 cannabinoids CB1 CB2 receptors CBs JWH201 JWH-201 JWH250 JWH-250 JWH 250 77.624510665918
9000736 JWH 203 864445-54-5 ≥98% 2011-02-21 73.687547154631 jwh-203 cannabinoids receptors JWH 250 JWH203 JWH-203 CB1 CB2 cannabimimetics forensics pain CBs binding analgesic 73.687547154631
10868 JWH 203 3-chlorophenyl isomer Exclusive 864445-56-7 ≥98% ✓ 2011-06-03 31.132707182320 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 31.132707182320
10867 JWH 203 4-chlorophenyl isomer Exclusive 864445-58-9 ≥98% ✓ 2011-06-02 36.822909760589 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 36.822909760589
10644 JWH 210 824959-81-1 ≥98% 2011-02-01 119.609337313713 jwh-210 cannabimimetic cannabinoids alklyindoles CB1 CB2 receptors agonists CBs JWH-210 JWH210 119.609337313713
9001038 JWH 210 2-ethylnaphthyl isomer Exclusive New - ≥98% ✓ 2011-10-11 51.995035048691 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 51.995035048691
9001039 JWH 210 3-ethylnaphthyl isomer New - ≥98% 2011-11-30 74.802596125547 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 74.802596125547
9001040 JWH 210 5-ethylnaphthyl isomer New - ≥98% 2011-11-17 59.643329679629 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 59.643329679629
9000771 JWH 210 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-08-10 44.869743788179 jwh-210-5-hydroxyindole-metabolite JWH-210 JWH210 cannabinoids CBs cannabimimetic metabolites CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum 44.869743788179
9001041 JWH 210 6-ethylnaphthyl isomer New - ≥98% 2012-01-31 206.657795692826 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 206.657795692826
9001042 JWH 210 7-ethylnaphthyl isomer Exclusive New 824960-64-7 ≥98% ✓ 2011-10-11 51.995035048691 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 51.995035048691
9001043 JWH 210 8-ethylnaphthyl isomer New - ≥95% 2011-11-04 53.097465114314 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 53.097465114314
10510 JWH 210-d9 New - ≥99% deuterated product 2011-09-08 48.455738971633 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 48.455738971633
10940 JWH 210 N-(4-hydroxypentyl) metabolite New - ≥95% 2012-01-19 126.559825701640 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 126.559825701640
10941 JWH 210 N-(5-carboxypentyl) metabolite Exclusive New - ≥98% ✓ 2011-10-11 51.668749500666 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 51.668749500666
9000772 JWH 210 N-(5-hydroxypentyl) metabolite New - ≥98% 2011-11-04 51.094067501825 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 51.094067501825
11153 JWH 249 New 864445-60-3 ≥98% 2012-02-10 0E-12 jwh-249 cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic JWH249 JWH-249 JWHs central peripheral 0E-12
13634 JWH 250 864445-43-2 ≥98% 2010-01-14 76.881878954195 jwh-250 cannabinoids CB1 CB2 receptors THC JWH-250 JWH250 Δ9-THC Δ9-tetrahydrocannabinols delta 9 tetrahydrocannabinols indoles cbs synthetic 76.881878954195
9000766 JWH 250 5-hydroxyindole metabolite Exclusive - ≥98% ✓ 2011-07-20 35.722872928177 jwh-250-5-hydroxyindole-metabolite JWH250 JWH-250 cannabinoids CBs cannabimimetics metabolite CB1 CB2 receptors agonists spices forensics synthetic smoking urinary urine serum 35.722872928177
10661 JWH 250-d5 Exclusive - ≥99% deuterated product ✓ 2011-02-14 32.813926949452 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 32.813926949452
10939 JWH 250 N-(4-hydroxypentyl) metabolite Exclusive New - ≥98% ✓ 2011-10-24 46.770100893042 jwh-250-n-4-hydroxypentyl-metabolite JWHs JWH-250 JWH250 metabolites cannabinoids CB1 CB2 CBs herbal smoke smoking forensics receptors agonist cannabimimetic metabolite metabolism 46.770100893042
10938 JWH 250 N-(5-carboxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-19 77.234958111501 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 77.234958111501
9000767 JWH 250 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-08-05 63.171820525698 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 63.171820525698
10578 JWH 251 864445-39-6 ≥98% 2010-08-20 53.611618745255 jwh-251 cannabinoids receptors JWHs JWH-251 JWH251 WIN55212-2 WIN 55212-2 CB1 CB2 cannabimimetics urine forensics cannabinoids cbs synthetic 53.611618745255
9001021 JWH 251 3-methylphenyl isomer Exclusive New - ≥98% ✓ 2011-10-11 26.198148018386 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 26.198148018386
9001022 JWH 251 4-methylphenyl isomer Exclusive New 864445-41-0 ≥98% ✓ 2011-10-14 23.715191259040 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 23.715191259040
10722 JWH 302 Exclusive 864445-45-4 ≥95% ✓ 2011-03-04 77.296232569548 jwh-302 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine forensics CBs JWH302 JWH-302 indoles central peripheral GTPγS binding 77.296232569548
10797 JWH 307 New 914458-26-7 ≥96% 2011-12-15 96.786584949347 jwh-307 JWH307 JWH-307 cannabinoids CBs CB1 CB2 herbal smoking forensics receptors agonists JWHs cannabimimetic psychological neurological nuerology toxicological toxicology 96.786584949347
10829 JWH 368 New 914458-31-4 ≥98% 2011-12-14 77.487867180509 jwh-368 JWH368 JWH-368 cannabinoids CBs CB1 CB2 herbal smoking forensics sciences receptors agonists cannabimimetic JWHs 77.487867180509
10828 JWH 369 New 914458-27-8 ≥95% 2012-01-25 121.627138556643 jwh-369 JWH369 JWH-369 cannabinoids cannabimimetics CB1 CB2 CBs receptors agonists spices forensics synthetic central peripheral mouse research 121.627138556643
10827 JWH 370 New 914458-22-3 ≥95% 2011-11-10 31.736608786711 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 31.736608786711
13636 JWH 398 Exclusive - ≥95% ✓ 2010-10-22 73.228542786809 jwh-398 jwh398 cannabinoids receptors WIN 55,212-2 CB1 CB2 cannabimimetics urine forensics CBs JWH-398 cbs synthetic 73.228542786809
9001023 JWH 398 2-chloronaphthyl isomer New - ≥95% 2011-11-09 40.013311857133 jwh-398-2-chloronaphthyl-isomer cannabinoids CBs cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic herbal mixtures isomers chloro naphthyl JWH398 JWH-398 JWHs 40.013311857133
9001024 JWH 398 3-chloronaphthyl isomer New - ≥98% 2012-01-11 109.267221717577 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 109.267221717577
9001025 JWH 398 5-chloronaphthyl isomer Exclusive New - ≥98% ✓ 2011-08-23 43.225616990506 jwh-398-5-chloronaphthyl-isomer JWH398 JWH-398 forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics central peripheral 43.225616990506
9001026 JWH 398 6-chloronaphthyl isomer New - ≥98% 2011-11-04 48.580300896462 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 48.580300896462
9001027 JWH 398 7-chloronaphthyl isomer New - ≥98% 2011-11-16 52.001222523293 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 52.001222523293
9001028 JWH 398 8-chloronaphthyl isomer New - ≥98% 2012-01-13 112.335403648117 jwh-398-8-chloronaphthyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic isomers herbal mixtures JWHs JWH-398 JWH398 central peripheral 112.335403648117
10514 JWH 398-d9 Exclusive New - ≥99% deuterated product ✓ 2011-08-25 50.086297295345 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 50.086297295345
9000770 JWH 398 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-06 58.087841707496 jwh-398-n-5-hydroxypentyl-metabolite JWH398 cannabinoids CBs JWH-398 forensic sciences JWHs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetics 58.087841707496
13158 JZL 184 1101854-58-3 ≥97% 2009-01-26 160.348107734806 jzl-184 2-AG 2AG MAGL inhibitors inhibits inhibition endocannabinoids pains analgesia MGL inhibitor JZL184 JZL-184 cannabinoids 160.348107734806
13668 JZL 195 - ≥98% 2010-02-10 120.234751381215 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 120.234751381215
10640 KM 233 Exclusive 628263-22-9 ≥98% ✓ 2011-07-07 35.974917127071 km-233 KM233 KM-233 CBs cannabinoids CB2 agonists recptors CB1 gliomas anti tumors cancers 35.974917127071
10009280 L-759,633 174627-50-0 >98% 2007-09-13 35.046546961326 l-759-633 L759633 cannabinoids receptors agonists CB1 CB2 endocrinology neurochemistry cannabinoids cbs synthetic 35.046546961326
10008618 Lauric Acid Leelamide - >98% 2006-09-05 0.520475138122 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 0.520475138122
10006148 Leelamine 1446-61-3 >98% 2006-05-10 0.520865561694 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 0.520865561694
10008614 Leelamine (hydrochloride) - ≥98% 2006-05-10 0.419208103131 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 0.419208103131
13453 LH 21 611207-11-5 ≥98% 2011-03-22 17.263738489871 lh-21 cannabimimetic CBs cannabinoids CB1 receptors antagonists pain weight gain obesity LH-21 LH21 central 17.263738489871
10563 MDA 19 1048973-47-2 ≥95% 2010-09-17 51.340761641673 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 51.340761641673
10639 MDA 77 Exclusive 1103774-21-5 ≥98% ✓ 2011-05-16 4.063591160221 mda-77 CB2 inverse agonists inflammation pain CB1 CBs cannabinoids peripheral MDA77 MDA-77 in vivo binds binding assay 4.063591160221
10979 MDMA methylene homolog (hydrochloride) Exclusive - ≥98% ✓ 2011-06-22 34.462629087627 mdma-methylene-homolog-hydrochloride 3,4-Methylenedioxymethamphetamine methyl homolog forensic sciences cannabinoids CBs pyrovalerones pentylones designer drugs forensics neuroscience psychoactive ecstasy HCl 34.462629087627
10007704 N-(3-hydroxyphenyl)-Arachidonoyl amide Exclusive 183718-75-4 >98% ✓ 2007-02-02 13.166132596685 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 13.166132596685
10007431 N-Arachidonoyl Dopamine-d8 - ≥99% deuterated product 2005-08-10 10.737403314917 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 10.737403314917
10005455 N-Arachidonoyl-L-Serine 187224-29-9 >98% 2004-08-11 7.638297338021 n-arachidonoyl-l-serine ARA-S endocannabinoids antagonists cannabidiols neuroprotective neurotransmitters hypotensive effects antagonize antagonist neurochemistry neuroscience cannabinoids cbs synthetic 7.638297338021
10005609 N-Oleoyl Taurine Exclusive 52514-04-2 ≥98% ✓ 2005-01-05 6.681187845304 n-oleoyl-taurine endocannibinoids fatty amides oleamides taurines amino-acyls lipidomics profiling fatty acids neurochemistry neuroscience TRPV1 TRPV4 FAAH cannabinoids cbs synthetic 6.681187845304
10006803 O-1602 317321-41-8 >98% 2005-09-12 10.751519337016 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 10.751519337016
10006804 O-1821 35482-50-9 >97% 2005-09-12 18.792081031307 o-1821 abnormal cannabidiol central cannabinoids peripheral CB1 CB2 receptors vasorelaxation neurochemistry neuroscience antagonists synthetic regioisomer endothelium dependent vasodilation cannabinoids cbs synthetic 18.792081031307
10004914 O-1918 536697-79-7 >98% 2005-09-09 9.388121546961 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 9.388121546961
10009195 O-2545 (hydrochloride) - >98% 2007-07-12 1.533701657459 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 1.533701657459
10007823 Oleoyl Ethanolamide-d2 - ≥99% deuterated product 2006-03-06 13.068480662984 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 13.068480662984
9000552 Oleoyl Ethanolamide-d4 Exclusive - ≥99% deuterated product ✓ 2010-01-12 10.002320441988 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 10.002320441988
10005459 Oleoyl Ethyl Amide Exclusive 85075-82-7 >98% ✓ 2004-07-21 21.423348066299 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 21.423348066299
10965 Palmitoleoyl Ethanolamide 94421-67-7 ≥98% 2011-06-27 20.597642725599 palmitoleoyl-ethanolamide POEA cannabinoids endocannabinoids CBs N-acylethanolamines signalling N-acylethanolamides NAEs signaling receptors pain lipid-derived 20.597642725599
13279 PF-3845 1196109-52-0 ≥98% 2010-01-27 37.992885205648 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 37.992885205648
71655 PHOP 288862-83-9 >98% 2005-02-02 10.937995264403 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 10.937995264403
10006973 Pravadoline 92623-83-1 ≥98% 2011-02-08 49.107296654389 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 49.107296654389
13621 Pristimerin Exclusive 1258-84-0 ≥98% ✓ 2010-03-08 42.875840568271 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 42.875840568271
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 35.607513812154 prostaglandin-d2-1-glyceryl-ester PGD2-1-glyceryl ester endocannabinoids anandamides 2AG fatty acids porcine brain isomerase moiety cannabinoids cbs synthetic 35.607513812154
10192 Prostaglandin D2 serinol amide - >98% 2004-05-13 39.763292817680 prostaglandin-d2-serinol-amide PGD2-SA PGD2 vasodilation prostaglandins brain sleep platelets aggregation anandamides serinols amides cannabinoids AEA 39.763292817680
10140 Prostaglandin E2-1-glyceryl ester 37497-47-5 >98% (as a 85:15 mixture of the 1- and 2-glyceryl esters) 48.040865561694 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 48.040865561694
14012 Prostaglandin E2 Ethanolamide Exclusive 194935-38-1 >98% ✓ 40.204841160221 prostaglandin-e2-ethanolamide PGE2-EA; Dinoprostone Ethanolamide; Prostamide E2 anandamides ethanolamides cannabinoids PGE2 prostaglandins AEA analogs neurochemistry neuroscience ethanolamines prostamides 40.204841160221
10193 Prostaglandin E2 serinol amide Exclusive - ≥98% ✓ 2004-03-03 36.258397790055 prostaglandin-e2-serinol-amide PGE2-SA PGE2SA cannabinoids agonists CB1 receptors analogs 2-glyceryl neurochemistry neuroscience 36.258397790055
10139 Prostaglandin F2α-1-glyceryl ester 43042-79-1 >98% (as a 9:1 mixture of the 2- and 1-glyceryl esters) 16.060359116022 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 16.060359116022
10194 Prostaglandin F2α serinol amide - >98% 2004-02-23 13.622338858195 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 13.622338858195
10004281 R-1 Methanandamide Phosphate - >98% 2004-08-20 17.891049723757 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 17.891049723757
10645 RCS-4 - ≥98% 2010-11-24 127.480315197521 rcs-4 cannabinoids receptors JWHs 018 CB1 CB2 cannabimimetics forensics CBs neurochemistry cannabinoids cbs synthetic 127.480315197521
10865 RCS-4 2-methoxy isomer - ≥98% 2011-06-15 54.039667490549 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 54.039667490549
10866 RCS-4 3-methoxy isomer Exclusive - ≥98% ✓ 2011-06-15 45.111948033066 rcs-4-3-methoxy-isomer cannabinoids receptors JWH 018 CB1 CB2 CBs cannabimimetics forensics synthetic bath salts JWH-018 JWH018 45.111948033066
10798 RCS-4-C4 homolog Exclusive - ≥98% ✓ 2011-04-21 58.428009777551 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 58.428009777551
10513 RCS-4-d9 New - ≥99% deuterated product 2011-09-12 44.447019892911 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 44.447019892911
10936 RCS-4 N-(4-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-07-29 38.576552595231 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 38.576552595231
10937 RCS-4 N-(5-carboxypentyl) metabolite - ≥98% 2011-06-28 44.108639866240 rcs-4-n-5-carboxypentyl-metabolite RCS4 RCS 4 forensics sciences cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices synthetics 44.108639866240
10935 RCS-4 N-(5-hydroxypentyl) metabolite Exclusive - ≥98% ✓ 2011-06-17 45.618204419889 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 45.618204419889
10636 RCS-8 Exclusive - ≥98% ✓ 2010-11-02 110.680693566903 rcs-8 SR-18 cannabinoids receptors JWH 250 CB1 CB2 cannabimimetics forensics cannabinoids cbs synthetic Rabbit Aorta Contracting Substance A2 Thromboxane Thromboxane A2 110.680693566903
10864 RCS-8 3-methoxy isomer Exclusive - ≥98% ✓ 2011-07-13 31.955627180866 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 31.955627180866
10863 RCS-8 4-methoxy isomer Exclusive - ≥95% ✓ 2011-07-13 38.326258650771 rcs-8-4-methoxy-isomer RCS8 RCS 8 isomers forensics sciences RCS4 RCS-4 CBs cannabinoids cannabimimetics CB1 CB2 receptors agonists spices synthetics 38.326258650771
9000484 Rimonabant 168273-06-1 ≥98% 2009-06-17 70.164019337016 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 70.164019337016
10899 (R)-(−)-JWH 073 N-(3-hydroxybutyl) metabolite New - ≥98% 2011-11-18 32.857078514426 -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 32.857078514426
10898 (S)-(+)-JWH 073 N-(3-hydroxybutyl) metabolite New - ≥98% 2011-11-18 31.907078514426 -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 31.907078514426
10009226 (±)-SLV 319 Exclusive 362519-49-1 >98% ✓ 2007-01-16 21.822596685082 -slv-319 CB1 CB2 Receptors Cannabinoids Antagonists Inflammations inflammatory neurochemistry lipophilic ligands cannabinoids cbs synthetic 21.822596685082
9000491 SR 144528 192703-06-3 ≥98% 2009-08-05 71.692483118478 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 71.692483118478
13830 Synthetic Cannabinoid HPLC Mixture I - ≥95% for each compound 2010-05-13 39.243082614455 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 39.243082614455
13850 Synthetic Cannabinoid HPLC Mixture II - ≥95% for each compound 2010-12-21 39.551017802333 synthetic-cannabinoid-hplc-mixture-ii cannabinoids CBs synthetics mixtures receptors agonists synthetic 39.551017802333
11337 Synthetic Cannabinoid HPLC Mixture V (AM Series) New - ≥95% for each compound 2012-02-02 101.640890116636 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 101.640890116636
13261 URB447 Exclusive 1132922-57-6 ≥98% ✓ 2009-06-18 32.550309392265 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 32.550309392265
10046 URB597 546141-08-6 >98% 54.148442993470 urb597 FAAH fatty acid amide hydrolases inhibitors URB-597 anandamides lipids inhibition selective selectivity AEA inhibits hydrolysis hydrolyze arachidonoyl cannabinoids ethanolamides neuroscience neurochemistry 54.148442993470
10007457 URB602 565460-15-3 >98% 2005-09-06 40.770787292817 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 40.770787292817
10007691 URB754 86672-58-4 >98% 2005-11-04 24.893955801105 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 24.893955801105
10674 URB937 Exclusive - ≥98% ✓ 2011-03-08 17.586224677716 urb937 FAAH anandamide AEA inhibitors peripheral pain Cannabinoids 17.586224677716
10009023 (+)WIN 55212-2 (mesylate) 131543-23-2 >98% 2006-10-05 47.709641060716 -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 47.709641060716
10736 (±)WIN 55212 (mesylate) New 137795-17-6 ≥98% 2012-01-11 110.382203395478 -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 110.382203395478
90215 α-Linolenoyl Ethanolamide Exclusive 57086-93-8 >98% ✓ 10.168516179952 -linolenoyl-ethanolamide cannabinoids neurotransmitters ethanolamides fatty acids CB alpha-linolenoyl .alpha.-linolenoyl cannabinergic neurochemistry neuroscience ethanolamines, cbs, synthetic 10.168516179952
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