化学
吡咯烷
前药
羧酸
立体化学
化学合成
氨基酸
有机化学
生物化学
体外
作者
Scott N. Mlynarski,Brian Aquila,Susan Cantin,Steve Cook,Aatman S. Doshi,M. Raymond V. Finlay,Eric T. Gangl,Tyler Grebe,Chungang Gu,Sameer Kawatkar,Jens Petersen,Petar Pop-Damkov,Alwin G. Schuller,Wenlin Shao,Jason D. Shields,Iain Simpson,Siavash Tavakoli,Sharon Tentarelli,Scott Throner,Haixia Wang,Jianyan Wang,Dedong Wu,Qing Ye
标识
DOI:10.1021/acs.jmedchem.4c02309
摘要
Arginase is a promising immuno-oncology target that can restore the innate immune response. However, it's highly polar active site often requires potent inhibitors to mimic amino acids, leading to poor passive permeability and low oral exposure. Using structure-based drug design, we discovered a novel proline-based arginase inhibitor (
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