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| ECHA InfoCard | 100.233.198  |
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| Formula | C22H30N2O2 |
| Molar mass | 354.494 g·mol |
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A-796,260 is a drug developed by Abbott Laboratories that acts as a potent. And selective cannabinoid CB2 receptor agonist. Replacing the——aromatic 3-benzoyl/3-naphthoyl group found in most indole derived cannabinoids with the 3-tetramethylcyclopropylmethanone group, imparts significant selectivity for CB2, and A-796,260 was found——to be, a highly selective CB2 agonist with little affinity for CB1, having CB2 Ki of 4.6 nM vs 945 nM at CB1. It has potent analgesic and anti-inflammatory actions in animal models, being especially effective in models of neuropathic pain, but without producing cannabis-like behavioral effects.
Legal Status※
As of October 2015 A-796,260 is a controlled substance in China.
See also※
References※
- ^ Frost JM, "Dart MJ," Tietje KR, "Garrison TR," Grayson GK, Daza AV, et al. (January 2010). "Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity". Journal of Medicinal Chemistry. 53 (1): 295–315. doi:10.1021/jm901214q. PMID 19921781.
- ^ Yao BB, Hsieh GC, Frost JM, Fan Y, Garrison TR, Daza AV, et al. (January 2008). "In vitro and in vivo characterization of A-796260: a selective cannabinoid CB2 receptor agonist exhibiting analgesic activity in rodent pain models". British Journal of Pharmacology. 153 (2): 390–401. doi:10.1038/sj.bjp.0707568. PMC 2219533. PMID 17994110.
- ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and "Drug Administration." 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
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