Crystal structure of HIV-1 protease inhibitor, KC32 complexed with wild-type protease
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Crystal structure of HIV-1 protease inhibitor, KC32 complexed with wild-type protease Descriptor: (5S)-N-{(1S,2R)-3-[(1,3-benzothiazol-6-ylsulfonyl)(2-methylpropyl)amino]-1-benzyl-2-hydroxypropyl}-2-oxo-3-[2-(trifluoromethyl)phenyl]-1,3-oxazolidine-5-carboxamide, ACETATE ION, HIV-1 protease, ... Authors: Nalam, M.N.L, Schiffer, C.A. Deposit date: 2010-05-07 Release date: 2010-11-10 Last modified: 2024-03-13 Method: X-RAY DIFFRACTION (1.85 Å) Cite: Structure-Based Design, Synthesis, and Structure-Activity Relationship Studies of HIV-1 Protease Inhibitors Incorporating Phenyloxazolidinones. J.Med.Chem., 53, 2010
创建时间：
2010-05-07
