JWH-167
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| Names | |
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| IUPAC name
2-phenyl-1-(1-pentylindol-3-yl)ethanone
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| Other names
1-(1-pentyl-1H-indol-3-yl)-2-phenylethanone
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| Identifiers | |
864445-37-4  |
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| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL365878  |
| ChemSpider | 23256084 |
| PubChem | 44397502 |
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| Properties | |
| C21H23NO | |
| Molar mass | 305.42 g·mol−1 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 verify (what is ?) |
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| Infobox references | |
JWH-167 (1-pentyl-3-(phenylacetyl)indole) is a synthetic cannabinoid from the phenylacetylindole family, which acts as a cannabinoid agonist with about 1.75x selectivity for CB1 with a Ki of 90nM ± 17 and 159nM ± 14 at CB2. Similar to the related 2'-methoxy compound JWH-250, and the 2'-chloro compound JWH-203, JWH-167 has a phenylacetyl group in place of the naphthoyl ring used in most aminoalkylindole cannabinoid compounds.[1][2]
References[edit]
- ^ Huffman JW, Szklennik PV, Almond A, Bushell K, Selley DE, He H, Cassidy MP, Wiley JL, Martin BR (2005). "1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles". Bioorganic & Medicinal Chemistry Letters. 15 (18): 4110–3. doi:10.1016/j.bmcl.2005.06.008. PMID 16005223.
- ^ Manera C, Tuccinardi T, Martinelli A (2008). "Indoles and related compounds as cannabinoid ligands". Mini reviews in medicinal chemistry. 8 (4): 370–87. doi:10.2174/138955708783955935. PMID 18473928.
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