JWH-210
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Systematic (IUPAC) name | |
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4-ethylnaphthalen-1-yl-(1-pentylindol-3-yl)methanone
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Clinical data | |
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Identifiers | |
CAS Number | 824959-81-1 ![]() Template:CAS (JWH-182) |
PubChem | CID: 45270396 |
ChemSpider | 24617616 |
Chemical data | |
Formula | C26H27NO |
Molecular mass | 369.498 g/mol |
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JWH-210 is an analgesic chemical from the naphthoylindole family, which acts as a potent cannabinoid agonist at both the CB1 and CB2 receptors, with Ki values of 0.46nM at CB1 and 0.69nM at CB2. It is one of the most potent 4-substituted naphthoyl derivatives in the naphthoylindole series, having a higher binding affinity (i.e. lower Ki) at CB1 than both its 4-methyl and 4-n-propyl homologues JWH-122 (CB1 Ki 0.69nM) and JWH-182 (CB1 Ki 0.65nM) respectively, and than the 4-methoxy compound JWH-081 (CB1 Ki 1.2nM).[2] It was discovered by and named after Dr. John W. Huffman.
JWH-210 may be neurotoxic to animals when administered in high doses.[3]
Legal Status
JWH-210 and JWH-122 were banned in Sweden on 1 October 2010 as hazardous goods harmful to health, after being identified as ingredients in "herbal" synthetic cannabis products.[4][5] The substances JWH-210, JWH-122 and JWH-203 were classified as illegal drugs by the Swedish government as of 1 September 2011.[6]
As of October 2015 JWH-210 is a controlled substance in China.[7]
See also
References
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- ↑ Swedish Code of Statutes Regulation (2010:1086).
- ↑ Swedish Code of Statutes Regulation (2010:1086). (pdf)
- ↑ LVFS 2011:8
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