Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
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Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides Descriptor: 4-biphenylacetyl-Cys-(D)Arg-Tyr-N-(2-phenylethyl) amide, Cathepsin L Authors: Chowdhury, S, Sivaraman, J, Wang, J, Devanathan, G, Lachance, P, Qi, H, Menard, R, Lefebvre, J, Konishi, Y, Cygler, M, Sulea, T, Purisima, E.O. Deposit date: 2002-08-21 Release date: 2002-12-11 Last modified: 2024-11-20 Method: X-RAY DIFFRACTION (1.9 Å) Cite: Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides J.Med.Chem., 45, 2002
创建时间：
2002-08-21
