Improved Feline Drugs as SARS-CoV-2 Mpro Inhibitors: Structure-Activity Studies & Micellar Solubilization for Enhanced Bioavailability
收藏Protein Data Bank Japan2023-10-18 更新2026-03-21 收录
下载链接：
https://pdbj.org/mine/summary/7lct
下载链接
链接失效反馈官方服务：
资源简介：
Improved Feline Drugs as SARS-CoV-2 Mpro Inhibitors: Structure-Activity Studies & Micellar Solubilization for Enhanced Bioavailability Descriptor: 3C-like proteinase, N-{(2S)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}-N~2~-{[(1S)-1-phenylethoxy]carbonyl}-L-leucinamide Authors: Khan, M.B, Arutyunova, E, Young, H.S, Lemieux, M.J. Deposit date: 2021-01-11 Release date: 2021-07-07 Last modified: 2023-10-18 Method: X-RAY DIFFRACTION (1.93 Å) Cite: Improved SARS-CoV-2 M pro inhibitors based on feline antiviral drug GC376: Structural enhancements, increased solubility, and micellar studies. Eur.J.Med.Chem., 222, 2021
创建时间：
2021-01-11
