作者:N. M. Gretskaya、A. A. Druzhinina、M. Yu. Bobrov、V. V. Bezuglov
DOI:10.1007/s10600-013-0566-4
日期:2013.5
Thiourethane analogs of anandamide and arachidonic acid amides with cyclopropylamine, dopamine, and serotonin that were capable of inhibiting hydrolysis of fatty-acid amides and interacting with cannabinoid receptor type 1 were synthesized for the first time.
首次合成了酰胺的硫脲醇类类似物,包括大麻素和花生四烯酸酰胺,带有环丙胺、多巴胺和血清素,能够抑制脂肪酸酰胺的水解并与大麻素受体类型1相互作用。