Design, Synthesis, and Biological Evaluation of Potent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2-Reference-Cited by-同舟云学术

Design, Synthesis, and Biological Evaluation of Potent Quinoline and Pyrroloquinoline Ammosamide Analogues as Inhibitors of Quinone Reductase 2

Published:2011-12-29 Issue:1 Volume:55 Page:367-377
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Reddy P. V. Narasimha¹,Jensen Katherine C.²,Mesecar Andrew D.²,Fanwick Phillip E.³,Cushman Mark¹

Affiliation:

1. Department of Medicinal Chemistry and Molecular Pharmacology, College of Pharmacy, and The Purdue University Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907, United States

2. Departments of Biological Sciences and Chemistry, and The Purdue University Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907, United States

3. Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm201251c

Reference41 articles.

1. The Ammosamides: Structures of Cell Cycle Modulators from a Marine-DerivedStreptomycesSpecies

2. Total Synthesis of the Ammosamides

3. Ammosamides A and B Target Myosin

4. Efficient Total Synthesis of Ammosamide B

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