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Structure paper

TitleDesign, synthesis, and biological evaluation of potent quinoline and pyrroloquinoline ammosamide analogues as inhibitors of quinone reductase 2.
Journal, issue, pagesJ. Med. Chem., Vol. 55, Page 367-377, Year 2012
Publish dateDec 5, 2011 (structure data deposition date)
AuthorsReddy, P.V. / Jensen, K.C. / Mesecar, A.D. / Fanwick, P.E. / Cushman, M.
External linksJ. Med. Chem. / PubMed:22206487
MethodsX-ray diffraction
Resolution1.5 - 1.53 Å
Structure data

PDB-3uxe:
Design, Synthesis and Biological Evaluation of Potent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors for Quinone Reductase 2
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

PDB-3uxh:
Design, Synthesis and Biological Evaluation of Potetent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2
Method: X-RAY DIFFRACTION / Resolution: 1.53 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-FAD:
FLAVIN-ADENINE DINUCLEOTIDE / FAD*YM

ChemComp-465:
8-amino-7-chloro-1-methyl-6-(methylideneamino)-2-oxo-1,2-dihydropyrrolo[4,3,2-de]quinoline-4-carboxamide

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

ChemComp-UXH:
6,8-diamino-7-chloro-1-methyl-2-oxo-1,2-dihydropyrrolo[4,3,2-de]quinoline-4-carboxamide

Source
  • homo sapiens (human)
KeywordsOXIDOREDUCTASE/INHIBITOR / Flavoprotein / quinone reductase / cytosol / OXIDOREDUCTASE-INHIBITOR complex

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