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

Research Area · Forensic Science

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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
9001133 2,3-Methylenedioxymethcathinone (hydrochloride) New - ≥98% 2012-01-26 188.724570602383 2-3-methylenedioxymethcathinone-hydrochloride 2,3-MDMC forensics phenethylamines cathinones designer drugs amphetamines bath salts party pills plants food hydrochloride HCl 188.724570602383
9001051 2,3-Methylenedioxy Pyrovalerone (hydrochloride) New - ≥98% 2011-11-28 93.296284591774 2-3-methylenedioxy-pyrovalerone-hydrochloride 2,3-MDPV designer drugs forensics bath salts psychoactive isomers plants food tablets 687603-66-3 93.296284591774
9001128 25I-NMBOMe New 1043868-97-8 ≥98% 2012-02-06 232.472329749104 25i-nmbome 919797-19-6 serotonin 5-HT2A hallucinogenic frontal cortex agonists forensic sciences phenethylamines neuroscience receptors brains memory schizophrenia hallucinogenic drugs 232.472329749104
11048 2-AI (hydrochloride) New 2338-18-3 ≥95% 2012-01-10 128.371991207437 2-ai-hydrochloride SU 8629; 2-Aminoindane 2975-41-9 MDAI 2-aminoindan phenethylamines phenylethylamines forensics indans indanes analgesia pain congeners psychoactive alkaloids synthesis stimulants SU 8629 SU-8629 SU8629 128.371991207437
10395 2C-E New 71539-34-9 ≥95% 2012-01-11 134.150318586106 2c-e 2,5-Dimethoxy-4-ethylphenethylamine forensics designer drugs phenethylamines serotonin norepinephrine dopamine monoamines oxidase inhibitors 2Cs psychoactive metabolism 4-ethyl-2,5-dimethoxy-phenethylamine 4-ethyl-2,5-dimethoxy-β-phenethylamine 134.150318586106
11113 2C-I (hydrochloride) New 64584-32-3 ≥98% 2012-01-17 204.681218637992 2c-i-hydrochloride forensics designer drugs phenethylamines serotonin norepinephrine dopamine monoamine oxidase inhibitors hydrochloride HCl psychoactive metabolism 2CI 2C I 204.681218637992
11199 2-Ethylethcathinone (hydrochloride) New - ≥98% 2012-02-10 48.152438155136 2-ethylethcathinone-hydrochloride 2-EEC forensics phenethylamines amphetamines cathinones designer drugs ethcathinones hydrochloride HCl 2EEC 2 EEC 48.152438155136
11419 2-Fluoroamphetamine (hydrochloride) New 1626-69-3 ≥98% 2012-02-07 168.532669142288 2-fluoroamphetamine-hydrochloride 2-FA 1716-60-5 designer drugs amphetamines phenethylamines bath salts monoamine neurotransmitters isomers 4-FA 4 FA 2 FA forensics hydrochloride HCl 168.532669142288
11229 2-Fluoroethcathinone (hydrochloride) Exclusive New - ≥98% 2012-01-27 134.362783009654 2-fluoroethcathinone-hydrochloride 2-FEC forensics phenethylamine cathinones designer drugs amphetamines hydrochloride HCl bath salts plants food pills 134.362783009654
11420 2-Fluoromethamphetamine (hydrochloride) Exclusive New - ≥98% 2012-02-09 127.104559268987 2-fluoromethamphetamine-hydrochloride 2-FMA methamphetamines forensic science stimulant 4-fluoromethamphetamine 4-FMA MDMA amphetamines 4FMA FMAs 127.104559268987
9001135 2-Fluoromethcathinone (hydrochloride) New - ≥98% 2011-12-07 154.594932677507 2-fluoromethcathinone-hydrochloride 2-FMC flephedrones cathinones analogs designer drugs plants feeders forensic analysis bath salts party pills food methcathinones designer psychoactive phenyl groups flephedrone hydrochloride 4FMC 4-FMC FMCs fluorines 154.594932677507
9001186 2-Methoxymethcathinone (hydrochloride) New - ≥98% 2012-02-06 263.450466910299 2-methoxymethcathinone-hydrochloride 2-MMC forensics phenethylamines amphetamines cathinones designer drugs isomers methedrone party pills bath salts hydrochloride HCl bronchodilator receptors agonists methoxyphenamine 2MMC 2 MMC 263.450466910299
11223 2-Methylmethcathinone (hydrochloride) New 1246815-51-9 ≥98% 2012-02-09 140.295513958342 2-methylmethcathinone-hydrochloride 2-MMC forensics science phenethylamines cathinones designer drugs amphetamines bath salts mephedrone 3MMC 4MMC MMCs 4-MMC 1246911-71-6 HCl cathinones 140.295513958342
11228 3,4-Dimethylethcathinone (hydrochloride) New - ≥95% 2012-01-23 126.364948789933 3-4-dimethylethcathinone-hydrochloride 3,4-DMEC hydrochloride HCl forensics phenethylamines cathinones designer drugs amphetamines psychoactive 126.364948789933
9001098 3,4-Dimethylmethcathinone (hydrochloride) New 1081772-06-6 ≥98% 2012-01-19 177.839535004769 3-4-dimethylmethcathinone-hydrochloride 3,4-DMMC 1082110-00-6 forensics phenethylamines cathinones designer drugs amphetamines hydrochloride HCl 4-methylmethcathinone 4-MMC 4 MMC 4MMC psychoactive bath salts plants food research 3,4 DMMC 3,4DMMC 177.839535004769
10437 3'4'-Methylenedioxy-α-pyrrolidinobutiophenone (hydrochloride) New 24622-60-4 ≥97% 2011-08-23 58.115568815438 3-4-methylenedioxy-pyrrolidinobutiophenone-hydrochloride MDPBP designer drugs forensics sciences stimulants PPP MDPV cathinones narcotics pyrrolidinoprophenone methylenedioxpyrovalerone 784985-33-7 58.115568815438
10439 3',4'-Methylenedioxy-α-pyrrolidinopropiophenone (hydrochloride) Exclusive New 24698-57-5 ≥97% 2011-08-24 42.097344748551 3-4-methylenedioxy-pyrrolidinopropiophenone-hydrochloride MDPPP designer drugs forensics sciences narcotics cathinones stimulants PPP MDPV Wistar rats methylenedioxypyrovalerone α-pyrrolidinopropiophenone 783241-66-7 42.097344748551
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
11198 3-Ethylethcathinone (hydrochloride) New - ≥98% 2012-01-24 156.618991201291 3-ethylethcathinone-hydrochloride 3-EEC 3EEC EECs forensics phenethylamines amphetamines cathinones designer drugs ethcathinones psychoactive 156.618991201291
9001082 3-Ethylmethcathinone (hydrochloride) New - ≥98% 2012-01-27 164.896184086192 3-ethylmethcathinone-hydrochloride 3-EMC designer drugs forensics hydrochloride HCl stimulants entactogen amphetamines phenethylamines cathinones mephedrone bath salts plants food tablets 164.896184086192
9001191 3-Fluoroamphetamine (hydrochloride) New 1716-59-2 ≥98% 2012-02-07 210.199335808955 3-fluoroamphetamine-hydrochloride 3-FA 1626-71-7 designer drugs amphetamines phenethylamines bath salts isomers 3 FA 4-FA 4 FA monoamine neurotransmitters hydrochloride HCl 210.199335808955
11230 3-Fluoroethcathinone (hydrochloride) New - ≥98% 2012-02-03 157.530908009654 3-fluoroethcathinone-hydrochloride 3-FEC forensics phenethylamine cathinones designer drugs amphetamines bath salts plants food pills hydrochloride HCl 157.530908009654
9001185 3-Fluoromethamphetamine (hydrochloride) New - ≥98% 2012-02-10 11.798895027624 3-fluoromethamphetamine-hydrochloride 3-FMA designer drugs amphetamines phenethylamines bath salts 4 FMA 4FMA stimulants methamphetamines powders isomers hydrochloride HCl forensics 3FMA 3 FMA 11.798895027624
10730 3-Fluoromethcathinone (hydrochloride) - ≥98% 2011-04-26 100.924141257072 3-fluoromethcathinone-hydrochloride 3-FMC flephedrones cathinones analogs designer drugs plant feeders forensic analysis CMF-3 1049677-77-1 100.924141257072
11222 3-Methylethcathinone (hydrochloride) New - ≥98% 2012-02-06 155.204106125184 3-methylethcathinone-hydrochloride 3-MEC forensics phenethylamines cathinones designer drugs amphetamines 3MEC 3 MEC hydrochloride HCl 155.204106125184
11224 3-Methylmethcathinone (hydrochloride) New 1246816-62-5 ≥97% 2012-02-03 200.664023225790 3-methylmethcathinone-hydrochloride 3-MMC 1246911-86-3 forensics phenethylamines cathinones designer drugs amphetamines synthetic bath salts powders mephedrone 3 MMC 4-MMC 4 MMC 4-methylmethcathinone 200.664023225790
11197 4-Ethylethcathinone (hydrochloride) New - ≥98% 2011-12-20 127.393142048571 4-ethylethcathinone-hydrochloride 4-EEC forensics phenethylamine cathinones designer drugs recreational psyhoactive 10801 9001069 4-methylethcathinone 4-MEC 4-methylmethcathinone 4-MMC HCl hydrochloride 127.393142048571
9001078 4-Ethylmethcathinone (hydrochloride) New - ≥97% 2011-11-10 94.304660968968 4-ethylmethcathinone-hydrochloride 4-EMC 1225622-14-9 designer drugs forensics stimulants entactogen amphetamine cathinone mephedrone bath salts plant food tablets 94.304660968968
11207 4-ethyl-N,N-Dimethylcathinone (hydrochloride) New - ≥98% 2011-12-19 102.670832347481 4-ethyl-n-n-dimethylcathinone-hydrochloride designer drugs forensics cathinones stimulatory amphetamines bath salts plants food tablets mephedrone HCl 4-methylmethcathinone 4-MMC hydrochloride 102.670832347481
11156 4-FA (hydrochloride) New 64609-06-9 ≥98% 2011-12-12 123.456671861263 4-fa-hydrochloride p-FA; para-Fluoroamphetamine 459-01-8 p-fluoroamphetamine PFA forensics monoamine inhibitors uptake dopamine serotonin norepinephrine designer drugs amphetamines inhibits inhibition serum urine GC/MS GC-MS mass spectrometry hydrochloride hcl halogenated psychostimulatory methamphetamine fluoroamphetamine 123.456671861263
11231 4-Fluoroethcathinone (hydrochloride) New - ≥98% 2012-01-16 130.117004166755 4-fluoroethcathinone-hydrochloride 4-FEC forensics phenethylamine cathinones designer drugs amphetamines psychoactive plants feeder capsules analogs ehtyl groups methyl amino flephedrone 4 FMC 4 FEC 130.117004166755
9001070 4-Fluoromethamphetamine (hydrochloride) 52063-62-4 ≥98% 2011-08-08 68.252000772342 4-fluoromethamphetamine-hydrochloride 4-FMA methamphetamines forensic sciences stimulants 4 fluoromethamphetamine 4FMA FMA MDMA amphetamines 4-fluoroamphetamine 351-03-1 68.252000772342
10859 4-Fluoromethcathinone (hydrochloride) 7589-35-7 ≥98% 2011-05-31 102.008874562155 4-fluoromethcathinone-hydrochloride 4-FMC; Flephedrone flephedrones 4-FMC cathionones analogs 4 FMC 4FMC derivatives drugs plants feeders forensics 447-40-5 102.008874562155
9000895 4-methoxy DMT New 3965-97-7 ≥98% 2011-11-21 96.998213852581 4-methoxy-dmt 4-MeO DMT; 4-methoxy-N,N-Dimethyltryptamine hallucinogen DMT dimethyltryptamine 5-HT receptors agonists 5-hydroxytryptamine behavior neuroscience forensics 4-OMe DMT 4 OMe DMT 4OMe DMT tryptamine 96.998213852581
10449 4'-Methoxy-α-pyrrolidinopropiophenone (tosylate) Exclusive New - ≥98% 2011-08-29 38.094499899571 4-methoxy-pyrrolidinopropiophenone-tosylate MOPPP analogs MDPV forensics sciences 478243-09-3 cathinones designer drugs 38.094499899571
9001069 4-Methylethcathinone (hydrochloride) Exclusive 1266688-86-1 ≥98% 2011-07-18 83.281241722824 4-methylethcathinone-hydrochloride 4-MEC; 4-methyl-N-ethyl Cathinone forensic sciences designer drugs methamphetamines 4methylethcathinone 4 methylethcathinones mephedrones cathinones analogs MDMA amphetamines plant feeders 1225617-18-4 83.281241722824
10801 4-Methylmethcathinone (hydrochloride) 1189726-22-4 ≥98% 2011-06-17 83.647718190009 4-methylmethcathinone-hydrochloride 4-MMC; 4-Methylephedrone; Mephedrone designer drugs methcathinone cathinones methamphetamine bath salts plants food feeder forensics psychoactive analysis hallucinogen meow bounce bubbles mad cow 4MMC MMC methylephedrone 1189805-46-6 4-methyl-methcathinone 83.647718190009
10448 4'-Methyl-α-pyrrolidinohexanophenone (hydrochloride) New - ≥98% 2011-10-21 21.055398696870 4-methyl-pyrrolidinohexanophenone-hydrochloride MPHP 34138-58-4 designer drugs forensics pyrovalerone bath salts MPPP PPP α-PPP α PPP psychostimulant toxic liver damage rabdomyloysis 21.055398696870
10446 4'-Methyl-α-pyrrolidinopropiophenone (hydrochloride) Exclusive New 1313393-58-6 ≥97% 2011-08-25 53.996528357980 4-methyl-pyrrolidinopropiophenone-hydrochloride MPPP designer drugs forensics pyrrolidinyl narcotics cathinones PPP metabolism stimulants MDMA receptors agonists analogs 28117-80-8 53.996528357980
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
11134 5-APB (hydrochloride) New 286834-80-8 ≥95% 2012-01-13 82.780268199234 5-apb-hydrochloride 5-(2-aminopropyl)benzofuran 6-APB benzofurans amphetamines phenethylamines MDA 5-APDB forensics designer drugs analogs stimulants entactogens 1-benzofuran-5yl-propan-2-amine 82.780268199234
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
11035 5-IAI (hydrochloride) New - ≥98% 2011-12-09 115.824291554659 5-iai-hydrochloride 5-iodo-2-Aminoindan 132367-76-1 phenethylamines phenylethylamines forensics indans indanes analogs MDMA rats serotonin hi hydrochloride hcl AI 5IAI psychoactive alkaloids 3,4-methylenedioxymethamphetamine 115.824291554659
10729 5-methoxy DALT Exclusive 928822-98-4 ≥95% 2011-04-05 97.452586634441 5-methoxy-dalt N,N-Diallyl-5-Methoxytryptamine tryptamines neuroscience forensics designer drugs 5-MeO-DALT MeO TRYPTAMINE, n,n-DIALLYL-5-METHOXY N,N-DIALLYL-5-METHOXYTRYPTAMINE INDOLE, 3-[2-(DIALLYLAMINO)ETHYL]-5-METHOXY 3-[2-(DIALLYLAMINO)ETHYL]-5-METHOXYINDOLE 5-Methoxy-DALT 5-MeO-DALT DALT 97.452586634441
90375 9-Octadecenamide 301-02-0 >98% 4.123281767955 9-octadecenamide Oleamide; cis-9-octadecenamide CSF sleep 9Z-octadecenamide fatty acids neurochemistry neuroscience 4.123281767955
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
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
9001125 bk-DMBDB (hydrochloride) New 17763-12-1 ≥98% 2011-11-15 58.471204116066 bk-dmbdb-hydrochloride 802286-83-5 designer drugs forensics psychotropic phenethylamines amphetamines cathinones bath salts plants food and tablets bkDMBDB bk DMBDB methylone 58.471204116066
9001124 bk-MDDMA (hydrochloride) New 109367-07-9 ≥98% 2011-11-15 58.119012317859 bk-mddma-hydrochloride Dimethylone 765231-58-1 designer drugs forensics psychotropic phenethylamines amphetamines cathinones bath salts plants food tablets methylone bkMDDMA bk MDDMA 58.119012317859
9001123 bk-MDEA (hydrochloride) New - ≥98% 2011-11-15 50.300664343339 bk-mdea-hydrochloride MDEC 1112937-64-0 designer drugs forensics ethylone psychtropic phenethylamines amphetamines cathinones bath salts plants food tablets metabolites urine bkMDEA bk MDEA 50.300664343339
11283 Buphedrone (hydrochloride) New 166593-10-8 ≥98% 2012-01-23 147.413092335708 buphedrone-hydrochloride MABP; α-methylamino-Butyrophenone forensics phenethylamines amphetamines cathinones designer drugs ethcathinones psychoactive hydrochloride HCl stimulants 408332-79-6 147.413092335708
10393 Butylone (hydrochloride) New 17762-90-2 ≥97% 2011-08-17 63.857263276041 butylone-hydrochloride β-keto MBDB designer drugs forensics receptors agonists bath salts MBDB MDMA cathinone methylbenzodioxolylbutanamine methylenedioxymethamphetamine 802575-11-7 butylone 63.857263276041
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
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
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
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
11160 D2PM (hydrochloride) New 172152-19-1 ≥98% 2012-01-03 75.067234383303 d2pm-hydrochloride Diphenylproplinol; Diphenyl-2-pyrrolidinemethanol designer drugs forensics cathinones hydrochloride HCl toxic humans organic synthesis Corey-Bakshi-Shibata catalysts Corey Bakshi Shibata psychoactive 75.067234383303
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
11241 Ethcathinone (hydrochloride) New 51553-17-4 ≥98% 2012-01-18 139.642585869217 ethcathinone-hydrochloride RMI 8201A; N-Ethylcathinone 71276-46-5 forensics phenethylamines cathinones designer drugs psychoactive recreational hydrochloride HCl amphetamines rats capsules tablets research N-monoethylcathinone RMI8201A RMI-8201A 139.642585869217
9001103 Eutylone (hydrochloride) New 17764-18-0 ≥98% 2011-12-15 91.020297925948 eutylone-hydrochloride β-keto-Ethylbenzodioxolylbutanamine; bk-EBDB designer drugs forensics cathinones bkEBDB bk EBDB amphetamines pyrovalerone psychotropic hydrochloride HCl entactogenic psychotropic butanamine ethylbenzodioxolyl 91.020297925948
10995 Harmaline New 304-21-2 ≥98% 2011-10-11 1.790779319947 harmaline inhibitors monoamine oxidases MAOI receptor agonists inverse agonists NMDA herbal mixtures forensics bath salts spices plants N-methyl-D-aspartate inhibits inhibition adulterant CBs cannabinoids hallucinogenic tryptamines 1.790779319947
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
10006350 HU-211 112924-45-5 ≥98% 2005-03-30 58.790282381829 hu-211 Dexanabinol HU211 endocannabinoids cannabis CB2 pain inflammation NF-kB NF-.kappa.B inhibition antioxidants neurochemistry terpene-based psychomotor DELTA9-THC .DELTA.9-THC D9-THC neuroprotective cannabidiols CB1 inflammatory pharmacology neuroscience neurochemistry 58.790282381829
90086 HU-308 256934-39-1 >98% 2005-03-16 35.176025663875 hu-308 endocannabinoids CB2 pain inflammation G-protein coupled receptors agonists hypotensives analgesics anti-inflammatory phenolic .DELTA.9-THC D9-THC CB1 FAAH fatty acid hydrolases substrates selective neuroscience neurochemistry GPCRs HU308 HU 308 cannabinoids 35.176025663875
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
9001007 JWH 018 2'-naphthyl-N-(1,1-dimethylpropyl) isomer New - ≥98% 2012-01-13 129.938282085955 jwh-018-2-naphthyl-n-1-1-dimethylpropyl-isomer cannabinoids CBs cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic isomers JWH018 JWH-018 JWH 18 JWH-18 JWH18 JWHs pejntyl chains indoles naphthyl moiety herbal blends central peripheral 129.938282085955
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
9001017 JWH 073 2'-naphthyl-N-(1,1-dimethylethyl) isomer New - ≥98% 2012-01-12 119.645204472316 jwh-073-2-naphthyl-n-1-1-dimethylethyl-isomer cannabinoids cannabimimetics CB1 CB2 receptors agonists spices forensics synthetic CBs herbal blends research applications isomers JWH073 JWH-073 JHW 73 JWH73 JWH-73 JWHs naphthyl groups butyl chains central peripheral 119.645204472316
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
9001049 JWH 081 8-methoxynaphthyl isomer New - ≥98% 2012-01-11 148.684279342982 jwh-081-8-methoxynaphthyl-isomer cannabinoids cannabimimetic CB1 CB2 receptors agonists spices forensics synthetic CBs ten-fold ten fold reduced reduces affinity isomers methoxy groups naphthyl rings central peripheral 148.684279342982
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
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
9001102 MDAI New 13274-81-2 ≥95% 2011-11-04 27.510141190915 mdai 5,6-Methylenedioxy-2-aminoindane designer drugs forensics MDA MDMA neuroscience neurotoxicity analogs amphetamine serotonin neurotoxin methamphetamine 12440-03-9 27.510141190915
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
9001140 Meconin New 569-31-3 ≥95% 2012-02-03 134.949305555555 meconin NSC 35547; Opianyl meconine opium heroin urinary urine metabolites forensics science opiates NSC-35547 NSC35547 134.949305555555
10529 Methedrone (hydrochloride) New 879665-92-6 ≥98% 2011-10-11 63.140864465314 methedrone-hydrochloride 4-Methedrone; Methoxyphedrine; PMMC; para-Methoxymethcathinone cathinone analogs MAO inhibitors PMMC mephedrone PMMA 530-54-1 inhibits inhibition phenethylamines amphetamines cathinones derivatives psychoactive MDMA hydrochloride HCl 63.140864465314
10624 Methylenedioxy Pyrovalerone Exclusive 687603-66-3 ≥98% 2011-01-07 41.186211080622 methylenedioxy-pyrovalerone MDPV 3,4-methylenedioxypyrovalerone inhibitors neurotransmitters dopamine norepinephrine MDMA ecstasy forensics designer drugs Hemihydrate Apomorphine Hydrochloride Anhydrous Apomorphine Hydrochloride Chloride Apomorphine Apomorphin Teclapharm Apomorphine Chloride Berberine Alkaloids Camptothecine Camptothecin Umbellatine Apomorphine Britaject Berberine Alkaloids Berbines Apokinon 41.186211080622
10679 Methylenedioxy Pyrovalerone-d8 (hydrochloride) 1246820-09-6 ≥99% deuterated product 2011-02-15 37.891464123511 methylenedioxy-pyrovalerone-d8-hydrochloride MDPV-d8 3,4-methylenedioxypyrovalerone inhibitors neurotransmitters dopamine norepinephrine MDMA ecstasy neuroscience forensics designer drugs deuterateds deuteriums GC/MS GC-MS LC/MS LC-MS mass spectrometry MS standards 37.891464123511
10684 Methylenedioxy Pyrovalerone (hydrochloride) 24622-62-6 ≥98% 2011-01-07 56.786631573859 methylenedioxy-pyrovalerone-hydrochloride MDPV 3,4-methylenedioxypyrovalerone inhibitors neurotransmitters dopamine norepinephrine MDMA ecstasy neuroscience forensics designer drugs 56.786631573859
10749 Methylhexanamine (hydrochloride) New 13803-74-2 ≥98% 2011-10-07 23.506575020663 methylhexanamine-hydrochloride Forthane; NSC 1106; DMAA; Geranamine; Floradrene; Dimethylamylamine stimulants designer drugs forensics sciences amphetamines amines nasal decongestant cerebral hemorrhage forthan methylhexaneamine 105-41-9 HCl allphatic floradrene 23.506575020663
10986 Methylone (hydrochloride) 186028-80-8 ≥98% 2011-07-13 53.463591850528 methylone-hydrochloride M1; bk-MDMA; 3,4-Methylenedioxy-N-methylcathinone forensics sciences M-1 M 1 amphetamines cathinones stimulants psychoactive designer drugs 186028-79-5 HCl bkMDMA MDMA ecstasy bath salts plants foods tablets monoaminergic systems 53.463591850528
11151 Mitragynine New 4098-40-2 ≥95% 2011-12-01 96.260735880908 mitragynine 9-methoxy Corynantheidine alkaloids forensics Mitragyna pain neuroscience opioids receptors agonists incense indoles plants noradreneric serotonergic metabolites 11047-39-5 36455-45-5 1383-32-0 6202-22-8 96.260735880908
11240 Naphyrone 1-naphthyl isomer (hydrochloride) New - ≥95% 2012-01-24 169.534477911646 naphyrone-1-naphthyl-isomer-hydrochloride designer drugs forensics pyrovalerone cathinones dopamine serotonin norepinephrine bath salts isomers hydrochloride HCl analogs party pills 169.534477911646
10517 Naphyrone (hydrochloride) New 850352-11-3 ≥97% 2011-08-29 119.314385553262 naphyrone-hydrochloride O-2482; NRG-1; Naphpyrovalerone; β-Naphyrone analogs MDPV forensics sciences designer drugs 850352-53-3 pyrovalerones cathinones dopamine serotonins norepinephrines bath salts 119.314385553262
9001144 N,N-Dimethylcathinone (hydrochloride) New 10105-90-5 ≥98% 2011-12-12 106.814633073045 n-n-dimethylcathinone-hydrochloride Metamfepramone forensics cathinone phenylethylamine phenethylamine neuroscience dimethylpropion dimepropion rats psychotropic hydrochloride hcl 106.814633073045
9000940 nor-Mephedrone (hydrochloride) Exclusive New 6941-17-9 ≥98% 2011-08-25 89.306772431460 nor-mephedrone-hydrochloride NSC 60487; Mephedrone Metabolite metabolites mephedrone NSC60487 NSC-60487 forensics sciences 31952-47-3 metabolism urine detection designer drugs 89.306772431460
11011 Pentedrone (hydrochloride) Exclusive New 879669-95-1 ≥98% 2011-08-23 85.426574239466 pentedrone-hydrochloride α-methylamino-Valerophenone analogs MDPV forensics sciences 879722-57-3 cathinones alkaloids psychotropics bath salts neurological HCl monoamine alkaloids methcathinone 85.426574239466
9000746 Pentylone (hydrochloride) 17763-01-8 ≥98% 2011-04-20 50.368140286714 pentylone-hydrochloride mephedrone MDMA ecstasy neuroscience forensics designer drugs MDPV valerophenone 1-pentanone pentanone 698963-77-8 50.368140286714
9000849 Phenazepam 51753-57-2 ≥98% 2011-02-14 12.435635359116 phenazepam Fenazepam; BD 98 benzodiazepine agonists GABAA receptors anxiolytic sedative anticonvulsive anti-convulsive anti convulsive hypnotic tranquilizers 12.435635359116
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
10817 Pyrovalerone Exclusive 3563-49-3 ≥95% 2011-05-25 40.680014376032 pyrovalerone Thymergix; Centroton; Valerophenone inhibitors neurotransmitters dopamine norepinephrine controlled substances forensic analysis forensics bath salts 10836 valerophenone 40.680014376032
10836 Pyrovalerone (hydrochloride) 1147-62-2 ≥95% 2011-05-24 45.364385875727 pyrovalerone-hydrochloride Centroton; Thymergix inhibitors neurotransmitters dopamine norepinephrine controlled substances forensic analysis forensics bath salts inhibition 10817 free base inhibits 3563-49-3 45.364385875727
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
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
9001095 (S)-2-Diphenylmethylpyrrolidine (hydrochloride) New 188398-87-0 ≥98% 2011-12-02 90.111953773925 -s-2-diphenylmethylpyrrolidine-hydrochloride (S)-Desoxy-D2PM NMR analysis dopamine transporter inhibitors stimulants psychoactive forensics 119237-64-8 inhibits inhibition desoxypipradrol 2-diphenylmethylpiperidine 90.111953773925
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
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
9001195 α-Pyrrolidinobutiophenone (hydrochloride) New 13415-54-8 ≥95% 2012-01-27 142.495838792477 -pyrrolidinobutiophenone-hydrochloride α-PBP 13415-82-2 hydrochloride HCl forensics phenethylamines amphetamines cathinones designer drugs butyrophenones ketones MPBP party pills synthetic anti-psychotic anti-emetic antipsychotic antiemetic anti psychtic anti emetic α-pyrrolidinobutyrophenone 142.495838792477
9001083 α-Pyrrolidinopentiphenone (hydrochloride) Exclusive New 5485-65-4 ≥98% 2011-10-11 60.351186131782 -pyrrolidinopentiphenone-hydrochloride α-PVP; 2-(1-pyrrolidinyl)-Valerophenone; O-2387 14530-33-7 designer drugs forensics pyrovalerone bath salts inhibits inhibitors inhibition transporters neurotransmitters dopamine norepinephrine uptake monoamine analogs alpha PVP APVP hydrochloride HCl psychoactive stimulant 60.351186131782
10445 α-Pyrrolidinopropiophenone (hydrochloride) Exclusive New 92040-10-3 ≥97% 2011-08-24 45.101250382089 -pyrrolidinopropiophenone-hydrochloride ɑ-PPP designer drugs forensics analogs diethylcathinone Wistar rats cathinone appetite suppressants PPP MPPP MDPPP αPPP alphaPPP alpha-pyrrolidinopropiophenone 19134-50-0 45.101250382089
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