Crystal structure of lopinavir bound to wild type HIV-1 protease
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Crystal structure of lopinavir bound to wild type HIV-1 protease Descriptor: N-{1-BENZYL-4-[2-(2,6-DIMETHYL-PHENOXY)-ACETYLAMINO]-3-HYDROXY-5-PHENYL-PENTYL}-3-METHYL-2-(2-OXO-TETRAHYDRO-PYRIMIDIN-1-YL)-BUTYRAMIDE, PHOSPHATE ION, Protease Authors: Schiffer, C.A, Nalam, M.N.L. Deposit date: 2007-06-01 Release date: 2007-09-04 Last modified: 2024-03-13 Method: X-RAY DIFFRACTION (1.95 Å) Cite: Design and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2' Ligands in Pseudosymmetric Dipeptide Isosteres. J.Med.Chem., 50, 2007
创建时间：
2007-06-01
