Lavendamycin Antitumor Agents: Structure-Based Design, Synthesis, and NAD(P)H:Quinone Oxidoreductase 1 (NQO1) Model Validation with Molecular Docking and Biological Studies-Reference-Cited by-同舟云学术

Lavendamycin Antitumor Agents: Structure-Based Design, Synthesis, and NAD(P)H:Quinone Oxidoreductase 1 (NQO1) Model Validation with Molecular Docking and Biological Studies

Published:2008-05-06 Issue:11 Volume:51 Page:3104-3115
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Hassani Mary¹,Cai Wen¹,Koelsch Katherine H.¹,Holley David C.¹,Rose Anthony S.¹,Olang Fatemeh¹,Lineswala Jayana P.¹,Holloway William G.¹,Gerdes John M.¹,Behforouz Mohammad¹,Beall Howard D.¹

Affiliation:

1. Center for Environmental Health Sciences, Department of Biomedical and Pharmaceutical Sciences, The University of Montana, Missoula, Montana 59812, Molecular Computational Core Facility, Center for Structural and Functional Neuroscience, Department of Biomedical and Pharmaceutical Sciences, The University of Montana, Missoula, Montana 59812, Department of Chemistry, Ball State University, Muncie, Indiana 47306

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm701066a

Reference69 articles.

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4. Structures of recombinant human and mouse NAD(P)H:quinone oxidoreductases: Species comparison and structural changes with substrate binding and release

5. The three-dimensional structure of NAD(P)H:quinone reductase, a flavoprotein involved in cancer chemoprotection and chemotherapy: mechanism of the two-electron reduction.

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