数量结构-活动关系
萨萨
化学
广告
分子动力学
异柠檬酸脱氢酶
立体化学
回转半径
合理设计
虚拟筛选
计算化学
生物化学
纳米技术
酶
生物
材料科学
有机化学
体外
古生物学
聚合物
作者
Yifan Wang,Shunjiang Jia,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,Shuo Wang,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,Yuwei Wang
摘要
Isocitrate dehydrogenase 1 (IDH1) is a necessary enzyme for cellular respiration in the tricarboxylic acid cycle. Mutant isocitrate dehydrogenase 1 (mIDH1) has been detected overexpressed in a variety of cancers. mIDH1 inhibitor ivosidenib (AG-120) was only approved by the Food and Drug Administration (FDA) for marketing, nevertheless, a range of resistance has been frequently reported. In this study, several mIDH1 inhibitors with the common backbone pyridin-2-one were explored using the three-dimensional structure-activity relationship (3D-QSAR), scaffold hopping, absorption, distribution, metabolism, excretion (ADME) prediction, and molecular dynamics (MD) simulations. Comparative molecular field analysis (CoMFA, R
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