Crystal Structure of Rhodesain in complex with a Macrolactam Inhibitor
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Crystal Structure of Rhodesain in complex with a Macrolactam Inhibitor Descriptor: (3~{S})-19-chloranyl-~{N}-(1-cyanocyclopropyl)-5-oxidanylidene-9-(trifluoromethyl)-12,17-dioxa-4-azatricyclo[16.2.2.0^{6,11}]docosa-1(21),6(11),7,9,18(22),19-hexaene-3-carboxamide, 1,2-ETHANEDIOL, Cysteine protease Authors: Dietzel, U, Kisker, C. Deposit date: 2017-11-07 Release date: 2018-04-11 Last modified: 2025-02-26 Method: X-RAY DIFFRACTION (1.6 Å) Cite: Repurposing a Library of Human Cathepsin L Ligands: Identification of Macrocyclic Lactams as Potent Rhodesain and Trypanosoma brucei Inhibitors. J. Med. Chem., 61, 2018
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2017-11-07
