A Unique Class of Duocarmycin and CC-1065 Analogues Subject to Reductive Activation-Reference-Cited by-同舟云学术

A Unique Class of Duocarmycin and CC-1065 Analogues Subject to Reductive Activation

Published:2007-11-17 Issue:49 Volume:129 Page:15391-15397
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Jin Wei¹,Trzupek John D.¹,Rayl Thomas J.¹,Broward Melinda A.¹,Vielhauer George A.¹,Weir Scott J.¹,Hwang Inkyu¹,Boger Dale L.¹

Affiliation:

1. Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, and Office of Therapeutics, Discovery and Development, University of Kansas Cancer Center, 3901 Rainbow Boulevard, Kansas City, Kansas 66160

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja075398e

Reference105 articles.

1. The structure of CC-1065, a potent antitumor agent and its binding to DNA

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4. Duocarmycins, Potent Antitumor Antibiotics Produced by Streptomyces sp. Structures and Chemistry.

5. Yatakemycin, a Novel Antifungal Antibiotic Produced by Streptomyces sp. TP-A0356.

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