生物信息学
数量结构-活动关系
部分
羟类固醇脱氢酶
醇脱氢酶
脱氢酶
化学
酒
生物化学
内科学
酶
医学
立体化学
基因
作者
Xiulian Yang,Shaowei Wang,Yunbing Tang,Yingfen Ying,Yang Zhu,Congde Chen,Ren‐Shan Ge,Miaoqing Liu
标识
DOI:10.1016/j.cbi.2024.111203
摘要
The use of salicylates as flavoring agents in food and beverages is common, but their potential to disrupt the endocrine system remains unclear. Human placental 3β-hydroxysteroid dehydrogenase 1 (h3β-HSD1) plays a role in progesterone synthesis and is the potential target. This study evaluated the inhibition of 13 salicylates on h3β-HSD1, structure-activity relationship (SAR) and compared with rat placental homolog r3β-HSD4. Salicylates inhibited h3β-HSD1, depending on carbon chain number in the alcohol moiety and the IC
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