Controlled Drugs and Substances Act
Schedule II
Source: Canadian Legal Information Institute (CanLII). Controlled Drugs and Substances Act, S.C. 1996, c. 19, as amended
3D rendering of ((3S)-2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl)-1-naphthalenyl-methanone
Effective 16 Jul 2015, SOR/2015-192 added:
2.
Synthetic cannabinoid receptor type 1 agonists, their salts, derivatives, isomers, and salts of derivatives and isomers—with the exception of ((3S)-2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl)-1-naphthalenyl-methanone (WIN 55,212-3) and its salts—including those that fall within the following core chemical structure classes:
3D rendering of 2-(Cyclohexyl)phenol
Effective 16 Jul 2015, SOR/2015-192 added:
(1)
Any substance that has a 2-(Cyclohexyl)phenol structure with substitution at the 1-position of the benzene ring by a hydroxy, ether or ester group and further substituted at the 5-position of the benzene ring, whether or not further substituted on the benzene ring to any extent, and substituted at the 3′-position of the cyclohexyl ring by an alkyl, carbonyl, hydroxyl, ether or ester, and whether or not further substituted on the cyclohexyl ring to any extent, including
3D rendering of Nabilone
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
Nabilone ((±)-trans-3-(1,1-Dimethylheptyl)-6,6a,7,8,10,10a-hexahydro-1-hydroxy-6,6-dimethyl-9H-dibenzo[b,d]pyran-9-one)
UK: MDA Part II Class B Section 1(c) Nabilone
US: CSA Schedule II Section f Subsection 1 Nabilone
CA: Previously at CDSA Schedule II Section 1 Subsection 5
⇒
PubChem: 5284592 39860; ChemSpider: 4447641; Wikipedia: Nabilone
3D rendering of Parahexyl
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
Parahexyl (3-Hexyl-6,6,9-trimethyl-7,8,9,10-tetrahydro-6H-dibenzo[b,d]pyran-1-ol)
UN: Psychotropics Schedule I Parahexyl
US: CSA Schedule I Section d Subsection 25 Parahexyl
CA: Previously at CDSA Schedule II Section 1 Subsection 6
⇒
PubChem: 8334; ChemSpider: 8031; Bluelight: Parahexyl; Wikipedia: Parahexyl
3D rendering of 3-(1,2-Dimethylheptyl)-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol
Effective 16 Jul 2015, SOR/2015-192 added:
(iii)
3-(1,2-Dimethylheptyl)-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo[b,d]pyran-1-ol (DMHP)
UN: Psychotropics Schedule I DMHP
CA: Previously at CDSA Schedule II Section 1 Subsection 7.1
⇒
PubChem: 36276; ChemSpider: 33359; Wikipedia: Dimethylheptylpyran
3D rendering of 5-(1,1-Dimethylheptyl)-2-(5-hydroxy-2-(3-hydroxypropyl)cyclohexyl)phenol
Effective 16 Jul 2015, SOR/2015-192 added:
(iv)
5-(1,1-Dimethylheptyl)-2-(5-hydroxy-2-(3-hydroxypropyl)cyclohexyl)phenol (CP 55,940)
⇒
PubChem: 104895; ChemSpider: 94668; Bluelight: CP 55,940; Wikipedia: CP 55,940
3D rendering of 5-(1,1-Dimethylheptyl)-2-(3-hydroxycyclohexyl)phenol
Effective 16 Jul 2015, SOR/2015-192 added:
(v)
5-(1,1-Dimethylheptyl)-2-(3-hydroxycyclohexyl)phenol (CP 47,497)
UK: MDA Part II Class B Section 1(c) CP 47,497
US: CSA Schedule I Section g Subsection 1 5-(1,1-Dimethylheptyl)-2-[(1R,3S)-3-hydroxycyclohexyl]-phenol
⇒
PubChem: 15942731; ChemSpider: 10205286; Drugs Forum: CP 47,497; Erowid: Spice Product; Wikipedia: CP 47,497
3D rendering of 3-(1-Naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(2)
Any substance that has a 3-(1-Naphthoyl)indole structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted on the naphthyl ring to any extent, including
UK: MDA Part II Class B Section 1(c) 3-(1-Naphthoyl)indole
US: CSA Schedule I Section ii Item ii 3-(1-Naphthoyl)indole
⇒
PubChem: 10355825; ChemSpider: 8531277
3D rendering of 1-Pentyl-3-(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
1-Pentyl-3-(1-naphthoyl)indole (JWH-018)
UK: MDA Part II Class B Section 1(c) JWH-018
US: CSA Schedule I Section g Subsection 3 1-Pentyl-3-(1-naphthoyl)indole
⇒
PubChem: 10382701; ChemSpider: 8558143; Bluelight: JWH-018; Drugs Forum: JWH-018; Erowid: Spice Product; Wikipedia: JWH-018
3D rendering of 1-Butyl-3-(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
1-Butyl-3-(1-naphthoyl)indole (JWH-073)
UK: MDA Part II Class B Section 1(c) JWH-073
US: CSA Schedule I Section g Subsection 4 1-Butyl-3-(1-naphthoyl)indole
⇒
PubChem: 10471670; ChemSpider: 8647081; Bluelight: JWH-073; Erowid: Spice Product; Wikipedia: JWH-073
3D rendering of 1-Pentyl-3-(4-methyl-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(iii)
1-Pentyl-3-(4-methyl-1-naphthoyl)indole (JWH-122)
UK: MDA Part II Class B Section 1(c) JWH-122
US: CSA Schedule I Section g Subsection 9 1-Pentyl-3-(4-methyl-1-naphthoyl)indole
⇒
PubChem: 44466638; ChemSpider: 24623066; Bluelight: JWH-122; Wikipedia: JWH-122
3D rendering of 1-Hexyl-3-(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
On 5 Feb 2016, 81 FR 6190 proposed to add:
(iv)
1-Hexyl-3-(1-naphthoyl)indole (JWH-019)
US: CSA Schedule I Section g Subsection 5 1-Hexyl-3-(1-naphthoyl)indole
⇒
PubChem: 52224389; ChemSpider: 24598813; Wikipedia: JWH-019
3D rendering of 1-(4-Pentenyl)-3-(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
On 5 Feb 2016, 81 FR 6190 proposed to add:
(v)
1-(4-Pentenyl)-3-(1-naphthoyl)indole (JWH-022)
⇒
Drugs Forum: JWH-022
3D rendering of 1-Butyl-3-(4-methoxy-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(vi)
1-Butyl-3-(4-methoxy-1-naphthoyl)indole (JWH-080)
3D rendering of 1-Butyl-3-(4-methoxy-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(vii)
1-Butyl-3-(4-methoxy-1-naphthoyl)indole (JWH-081)
UK: MDA Part II Class B Section 1(c) JWH-081
US: CSA Schedule I Section g Subsection 8 1-Pentyl-3-[1-(4-methoxynaphthoyl)]indole
⇒
PubChem: 10547208; ChemSpider: 8722599; Wikipedia: JWH-081
3D rendering of 1-(2-Morpholin-4-ylethyl)-3-(1naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(viii)
1-(2-Morpholin-4-ylethyl)-3-(1naphthoyl)indole (JWH-200)
UK: MDA Part II Class B Section 1(c) JWH-200
US: CSA Schedule I Section g Subsection 6 1-[2-(4-Morpholinyl)ethyl]-3-(1-naphthoyl)indole
⇒
PubChem: 10045570; ChemSpider: 8221134; Drugs Forum: JWH-200; Erowid: Spice Product; Wikipedia: JWH-200
3D rendering of 1-Pentyl-3-(4-ethyl-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
On 5 Feb 2016, 81 FR 6190 proposed to add:
(ix)
1-Pentyl-3-(4-ethyl-1-naphthoyl)indole (JWH-210)
⇒
PubChem: 45270396; ChemSpider: 24617616; Wikipedia: JWH-210
3D rendering of 1-Pentyl-3-(2-methoxy-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
On 5 Feb 2016, 81 FR 6190 proposed to add (and to renumber subsequent entries):
(x)
1-Pentyl-3-(2-methoxy-1-naphthoyl)indole (JWH-267)
3D rendering of 1-[(N-Methylpiperidin-2-yl)methyl]-3(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(xi)
1-[(N-Methylpiperidin-2-yl)methyl]-3(1-naphthoyl)indole (AM-1220)
⇒
PubChem: 9929889; ChemSpider: 8105520; Wikipedia: AM-1220
3D rendering of 1-(5-Fluoropentyl)-3-(1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(xii)
1-(5-Fluoropentyl)-3-(1-naphthoyl)indole (AM-2201)
UK: MDA Part II Class B Section 1(c) AM-2201
US: CSA Schedule I Section g Subsection 11 1-(5-Fluoropentyl)-3-(1-naphthoyl)indole
⇒
PubChem: 53393997; ChemSpider: 24751884; Drugs Forum: AM-2201; Wikipedia: AM-2201
3D rendering of 1-(5-Fluoropentyl)-3-(4-methyl-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(xiii)
1-(5-Fluoropentyl)-3-(4-methyl-1-naphthoyl)indole (MAM-2201)
⇒
PubChem: 66570720; ChemSpider: 28289977; Bluelight: MAM-2201; Drugs Forum: MAM-2201; Wikipedia: MAM-2201
3D rendering of 1-(5-Fluoropentyl)-3-(4-ethyl-1-naphthoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(xiv)
1-(5-Fluoropentyl)-3-(4-ethyl-1-naphthoyl)indole (EAM-2201)
3D rendering of ((3R)-2,3-Dihydro-5-methyl-3(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl)-1-naphthalenyl-methanone
Effective 16 Jul 2015, SOR/2015-192 added:
(xv)
((3R)-2,3-Dihydro-5-methyl-3(4-morpholinylmethyl)pyrrolo[1,2,3-de]-1,4-benzoxazin-6-yl)-1-naphthalenyl-methanone (WIN 55212-2)
⇒
PubChem: 5311501; ChemSpider: 4470978; Bluelight: WIN 55,212-2; Drugs Forum: WIN 55,212-2; Wikipedia: WIN_55,212-2
3D rendering of 3-(1-Naphthoyl)pyrrole
Effective 16 Jul 2015, SOR/2015-192 added:
(3)
Any substance that has a 3-(1-Naphthoyl)pyrrole structure with substitution at the nitrogen atom of the pyrrole ring, whether or not further substituted on the pyrrole ring to any extent and whether or not substituted on the naphthyl ring to any extent, including
UK: MDA Part II Class B Section 1(c) 3-(1-Naphthoyl)pyrrole
US: CSA Schedule I Section iii Item iii 3-(1-Naphthoyl)pyrrole
⇒
PubChem: 15832251; ChemSpider: 10506445
3D rendering of 1-Pentyl-5-(2-fluorophenyl)-3-(1-naphthoyl)pyrrole
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
1-Pentyl-5-(2-fluorophenyl)-3-(1-naphthoyl)pyrrole (JWH-307)
⇒
PubChem: 16049783; ChemSpider: 13178178; Drugs Forum: JWH-307; Wikipedia: JWH-307
3D rendering of 3-Phenylacetylindole
Effective 16 Jul 2015, SOR/2015-192 added:
(4)
Any substance that has a 3-Phenylacetylindole structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted on the phenyl ring to any extent, including
UK: MDA Part II Class B Section 1(c) 3-Phenylacetylindole
US: CSA Schedule I Section v Item v 3-Phenylacetylindole
⇒
PubChem: 266609; ChemSpider: 234313; Drugs Forum: Phenylacetylindoles
3D rendering of 1-Pentyl-3-(2-methoxyphenylacetyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
1-Pentyl-3-(2-methoxyphenylacetyl)indole (JWH-250)
UK: MDA Part II Class B Section 1(c) JWH-250
US: CSA Schedule I Section g Subsection 7 1-Pentyl-3-(2-methoxyphenylacetyl)indole
⇒
PubChem: 44397540; ChemSpider: 23256117; Drugs Forum: JWH-250; Wikipedia: JWH-250
3D rendering of 1-Pentyl-3-(2-methylphenylacetyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
1-Pentyl-3-(2-methylphenylacetyl)indole (JWH-251)
⇒
PubChem: 11616723; ChemSpider: 9791472; Drugs Forum: JWH-251; Wikipedia: JWH-251
3D rendering of 1-Pentyl-3-(3-methoxyphenylacetyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(iii)
1-Pentyl-3-(3-methoxyphenylacetyl)indole (JWH-302)
3D rendering of 3-Benzoylindole
Effective 16 Jul 2015, SOR/2015-192 added:
(5)
Any substance that has a 3-Benzoylindole structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted on the phenyl ring to any extent, including
UK: MDA Part II Class B Section 1(c) 3-Benzoylindole
US: CSA Schedule I Section v Item v 3-Benzoylindole
⇒
PubChem: 84845; ChemSpider: 76537
3D rendering of 1-(1-Methylpiperidin-2-ylmethyl)-3-(2-iodobenzoyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
1-(1-Methylpiperidin-2-ylmethyl)-3-(2-iodobenzoyl)indole (AM-2233)
⇒
PubChem: 10226340; ChemSpider: 8401830; Drugs Forum: AM-2233; Wikipedia: AM-2233
3D rendering of 3-Methanone(cyclopropyl)indole
Effective 16 Jul 2015, SOR/2015-192 added:
(6)
Any substance that has a 3-Methanone(cyclopropyl)indole structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted on the cyclopropyl ring to any extent, including
The Open Parser for Systematic IUPAC nomenclature (OPSIN), a superlative work of software design and engineering in my view, quite properly says “3-methanone(cyclopropyl)indole” circumvents the rules and offends the language of chemistry: “3-methanone(cyclopropyl)indole has no tokens unknown to OPSIN but does not conform to its grammar. From left to right it is unparsable due to the following being uninterpretable:(cyclopropyl)indole”
3D rendering of (1-Pentyl-1H-indol-3-yl)(2,2,3,3- tetramethylcyclopropyl)-methanone
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
(1-Pentyl-1H-indol-3-yl)(2,2,3,3- tetramethylcyclopropyl)-methanone (UR-144)
UK: MDA Part II Class B Section 1(c) UR-144
US: CSA Schedule I Section h Subsection 1 (1-Pentyl-1H-indol-3-yl)(2,2,3,3- tetramethylcyclopropyl)methanone
US: [proposed] CSA Schedule I Section g Subsection 16 (1-Pentyl-1H-indol-3-yl)(2,2,3,3- tetramethylcyclopropyl)methanone
⇒
PubChem: 44626619; ChemSpider: 24634882; Bluelight: UR-144; Drugs Forum: UR-144; Wikipedia: UR-144
3D rendering of [1-(5-Fluoro-pentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-methanone
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
[1-(5-Fluoro-pentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)-methanone (5F-UR-144)
UK: MDA Part II Class B Section 1(c) XLR11
US: CSA Schedule I Section h Subsection 2 [1-(5-Fluoro-pentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
US: [proposed] CSA Schedule I Section g Subsection 17 [1-(5-Fluoro-pentyl)-1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone
⇒
PubChem: 57501498; ChemSpider: 28537382; Bluelight: XLR11; Wikipedia: XLR-11 (drug)
3D rendering of (1-(2-(4-Morpholinyl)ethyl)-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)-methanone
Effective 16 Jul 2015, SOR/2015-192 added:
(iii)
(1-(2-(4-Morpholinyl)ethyl)-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)-methanone (A-796,260)
⇒
PubChem: 11584525; ChemSpider: 9759290; Wikipedia: A-796,260
3D rendering of Quinolin-8-yl 1H-indole-3-carboxylate
Effective 16 Jul 2015, SOR/2015-192 added:
(7)
Any substance that has a Quinolin-8-yl 1H-indole-3-carboxylate structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted on the quinolin-8-yl ring to any extent, including
3D rendering of 1-Pentyl-8-quinolinyl ester-1H-indole-3-carboxylic acid
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
1-Pentyl-8-quinolinyl ester-1H-indole-3-carboxylic acid (PB-22)
The Open Parser for Systematic IUPAC nomenclature (OPSIN), a superlative work of software design and engineering in my view, quite properly says “1-Pentyl-8-quinolinyl ester-1H-indole-3-carboxylic acid” circumvents the rules and offends the language of chemistry: “1-Pentyl-8-quinolinyl ester-1H-indole-3-carboxylic acid could be parsed but OPSIN was unsure of the meaning of the words. This error will occur, by default, if a name is just a substituent”
US: CSA Schedule I Section h Subsection 7 Quinolin-8-yl 1-pentyl-1H-indole-3-carboxylate
⇒
PubChem: 71604304; ChemSpider: 29339966; Drugs Forum: QUPIC; Wikipedia: QUPIC
3D rendering of 1-(5-Fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
1-(5-Fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid (5F-PB-22)
The Open Parser for Systematic IUPAC nomenclature (OPSIN), a superlative work of software design and engineering in my view, quite properly says “1-(5-Fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid” circumvents the rules and offends the language of chemistry: “1-(5-Fluoropentyl)-8-quinolinyl ester-1H-indole-3-carboxylic acid could be parsed but OPSIN was unsure of the meaning of the words. This error will occur, by default, if a name is just a substituent”
US: CSA Schedule I Section h Subsection 8 Quinolin-8-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate
⇒
PubChem: 72710774; ChemSpider: 29341631; Drugs Forum: 5F-PB-22; Wikipedia: 5F-PB-22
3D rendering of 3-Carboxamideindazole
Effective 16 Jul 2015, SOR/2015-192 added:
(8)
Any substance that has a 3-Carboxamideindazole structure with substitution at the nitrogen atom of the indazole ring, whether or not further substituted on the indazole ring to any extent and whether or not substituted at the carboxamide group to any extent, including
The Open Parser for Systematic IUPAC nomenclature (OPSIN), a superlative work of software design and engineering in my view, quite properly says “3-Carboxamideindazole” circumvents the rules and offends the language of chemistry: “3-Carboxamideindazole was uninterpretable due to the following section of the name: 3-Carboxamide The following was not understandable in the context it was used: oxamide”
3D rendering of N-(Adamantan-1-yl)-1-pentyl-1H-indazole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
N-(Adamantan-1-yl)-1-pentyl-1H-indazole-3-carboxamide (AKB48)
US: CSA Schedule I Section h Subsection 3 N-(1-Adamantyl)-1-pentyl-1H-indazole-3-carboxamide
US: [proposed] CSA Schedule I Section g Subsection 18 N-(1-Adamantyl)-1-pentyl-1H-indazole-3-carboxamide
⇒
PubChem: 57404063; ChemSpider: 28189076; Bluelight: AKB48; Drugs Forum: AKB48; Wikipedia: AKB48 (drug)
3D rendering of N-(Adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
N-(Adamantan-1-yl)-1-(5-fluoropentyl)-1H-indazole-3-carboxamide (5F-AKB48)
⇒
PubChem: 71711119; ChemSpider: 29339965; Drugs Forum: 5F-AKB48
3D rendering of N-(1-(Aminocarbonyl)-2-methylpropyl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(iii)
N-(1-(Aminocarbonyl)-2-methylpropyl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide (AB-FUBINACA)
US: CSA Schedule I Section h Subsection 9 N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide
⇒
PubChem: 58124325; ChemSpider: 28537614; Wikipedia: AB-FUBINACA
3D rendering of N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(iv)
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide (AB-PINACA)
US: CSA Schedule I Section h Subsection 22 N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide
⇒
PubChem: 71301472; ChemSpider: 28537615; Wikipedia: AB-PINACA
3D rendering of 3-Carboxamideindole
Effective 16 Jul 2015, SOR/2015-192 added:
(9)
Any substance that has a 3-Carboxamideindole structure with substitution at the nitrogen atom of the indole ring, whether or not further substituted on the indole ring to any extent and whether or not substituted at the carboxamide group to any extent, including
The Open Parser for Systematic IUPAC nomenclature (OPSIN), a superlative work of software design and engineering in my view, quite properly says “3-carboxamideindole” circumvents the rules and offends the language of chemistry: “3-carboxamideindole was uninterpretable due to the following section of the name: 3-carboxamide The following was not understandable in the context it was used: oxamide”
3D rendering of N-(Adamantan-1-yl)-1-fluoropentylindole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(i)
N-(Adamantan-1-yl)-1-fluoropentylindole-3-carboxamide (STS-135)
⇒
PubChem: 57404059; ChemSpider: 28189067; Bluelight: STS-135; Drugs Forum: STS-135; Wikipedia: STS-135 (drug)
3D rendering of N-(Adamantan-1-yl)-1-pentylindole-3-carboxamide
Effective 16 Jul 2015, SOR/2015-192 added:
(ii)
N-(Adamantan-1-yl)-1-pentylindole-3-carboxamide (APICA)
⇒
PubChem: 71308155; ChemSpider: 29341717; Drugs Forum: SDB-001; Wikipedia: SDB-001
11 March 2016 · Creative Commons BY-NC-SA ·