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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 8.0 nM at CB1 and 7.0 nM at CB2. It was originally discovered by, and named after, 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.

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  • JWH-203 (en)
  • JWH-203 (pl)
  • JWH-203 (ru)
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  • JWH-203 – organiczny związek chemiczny, syntetyczny kanabinoid zsyntezowany przez Johna W. Huffmana (stąd akronim JWH). W Polsce od 2011 roku jest w grupie I-N Ustawy o przeciwdziałaniu narkomanii. (pl)
  • JWH-203 (1-пентил-3-(2-хлорфенилацетил)индол) — анальгетик, , действующий как каннабиноидный агонист с практически равным сродством с CB1 и CB2 рецепторами. Так, ингибиторная константа, показывающая степень сродства к CB1, составляет 8 нМ. Был создан химиком Джоном Хаффманом в экспериментальных целях, откуда и сокращение «JWH». (ru)
  • 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 8.0 nM at CB1 and 7.0 nM at CB2. It was originally discovered by, and named after, 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. (en)
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legal DE
  • Anlage II (en)
legal status
  • I-N (en)
legal UK
  • Class B (en)
legal US
  • Schedule I (en)
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  • Clc2ccccc2CCc1cnc3ccccc13 (en)
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  • YDINKDBAZJOSLV-UHFFFAOYSA-N (en)
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