3UXH
Design, Synthesis and Biological Evaluation of Potetent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2
Summary for 3UXH
Entry DOI | 10.2210/pdb3uxh/pdb |
Related | 3UXE |
Descriptor | Ribosyldihydronicotinamide dehydrogenase [quinone], ZINC ION, FLAVIN-ADENINE DINUCLEOTIDE, ... (5 entities in total) |
Functional Keywords | quinone reductase, cytosol, oxidoreductase-inhibitor complex, oxidoreductase/inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Cytoplasm: P16083 |
Total number of polymer chains | 2 |
Total formula weight | 53983.98 |
Authors | Cushman, M.,Mesecar, A.D.,Fanwick, P.E.,Narasimha, R.,Jensen, K.C. (deposition date: 2011-12-05, release date: 2012-01-18, Last modification date: 2024-05-22) |
Primary citation | Reddy, P.V.,Jensen, K.C.,Mesecar, A.D.,Fanwick, P.E.,Cushman, M. Design, synthesis, and biological evaluation of potent quinoline and pyrroloquinoline ammosamide analogues as inhibitors of quinone reductase 2. J.Med.Chem., 55:367-377, 2012 Cited by PubMed: 22206487DOI: 10.1021/jm201251c PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.53 Å) |
Structure validation
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