作者:S.Y. Sit、Charles M. Conway、Kai Xie、Robert Bertekap、Clotilde Bourin、Kevin D. Burris
DOI:10.1016/j.bmcl.2009.11.080
日期:2010.2
A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition
一系列新的肟氨基甲酸酯已被确定为内源性大麻素信号系统关键调节酶脂肪酸酰胺水解酶(FAAH)的有效抑制剂。在这封信中,介绍了这种新型FAAH抑制剂的发现和生物学评估背后的原理。讨论了选定靶标的体外和体内结果,以及抑制动力学和分子模型研究。1个