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・ JWH-133
・ JWH-147
・ JWH-148
・ JWH-149
・ JWH-161
・ JWH-164
・ JWH-167
・ JWH-175
・ JWH-176
・ JWH-184
・ JWH-185
・ JWH-193
・ JWH-196
・ JWH-198
・ JWH-200
JWH-203
・ JWH-210
・ JWH-249
・ JWH-250
・ JWH-251
・ JWH-302
・ JWH-307
・ JWH-359
・ JWH-398
・ JWH-424
・ Jwibulnori
・ Jwipo
・ Jwira-Pepesa language
・ JWK
・ JWL


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JWH-203 : ウィキペディア英語版
JWH-203

JWH-203 (1-pentyl-3-(2-chlorophenylacetyl)indole) is an analgesic chemical from the phenylacetylindole family that acts as a cannabinoid agonist with approximately equal affinity at both the CB1 and CB2 receptors, having a Ki of 8.0nM at CB1 and 7.0nM at CB2. It was originally discovered by, and named after, Dr. John W. Huffman, but has subsequently been sold without his permission as an ingredient of synthetic cannabis smoking blends. Similar to the related 2'-methoxy compound JWH-250, the 2'-bromo compound JWH-249, and the 2'-methyl compound JWH-251, JWH-203 has a phenylacetyl group in place of the naphthoyl ring used in most aminoalkylindole cannabinoid compounds, and has the strongest ''in vitro'' binding affinity for the cannabinoid receptors of any compound in the phenylacetyl group.
Unexpectedly despite its weaker CB1 Ki ''in vitro'', the 2-methylindole derivative JWH-204 is actually more potent than JWH-203 in animal tests for cannabinoid activity, though it is still weaker than JWH-249.
==Legal Status==

As of October 2015 JWH-203 is a controlled substance in China.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「JWH-203」の詳細全文を読む



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