二氢月桂酸脱氢酶
药物发现
可药性
特瑞氟米特
IC50型
化学
药品
计算生物学
生物化学
对接(动物)
药理学
李宾斯基五定律
喹唑啉
酶
生物
组合化学
医学
体外
生物信息学
芬戈莫德
免疫学
护理部
基因
多发性硬化
作者
William T. Higgins,Sandip Vibhute,Chad Bennett,Steffen Lindert
标识
DOI:10.1021/acs.jcim.3c01358
摘要
We used a structure-based drug discovery approach to identify novel inhibitors of human dihydroorotate dehydrogenase (DHODH), which is a therapeutic target for treating cancer and autoimmune and inflammatory diseases. In the case of acute myeloid leukemia, no previously discovered DHODH inhibitors have yet succeeded in this clinical application. Thus, there remains a strong need for new inhibitors that could be used as alternatives to the current standard-of-care. Our goal was to identify novel inhibitors of DHODH. We implemented prefiltering steps to omit PAINS and Lipinski violators at the earliest stages of this project. This enriched compounds in the data set that had a higher potential of favorable oral druggability. Guided by Glide SP docking scores, we found 20 structurally unique compounds from the ChemBridge EXPRESS-pick library that inhibited DHODH with IC
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