Design, Synthesis, and Structure−Activity Relationships of Haloenol Lactones: Site-Directed and Isozyme-Selective Glutathione S-Transferase Inhibitors-Reference-Cited by-同舟云学术

Design, Synthesis, and Structure−Activity Relationships of Haloenol Lactones: Site-Directed and Isozyme-Selective Glutathione S-Transferase Inhibitors

Published:2004-05-04 Issue:12 Volume:47 Page:3282-3294
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Wu Zhixing¹,Minhas Gurpreet Singh¹,Wen Dingyi¹,Jiang Hualiang¹,Chen Kaixian¹,Zimniak Piotr¹,Zheng Jiang¹

Affiliation:

1. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 200031, China, Department of Pharmaceutical Sciences, School of Pharmacy, Bouvé College of Health Sciences, Northeastern University, Boston, Massachusetts 02115, Biogen Idec, Cambridge, Massachusetts 02412, and Department of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0499615

Reference40 articles.

1. Characterization of melphalan-glutathione adducts whose formation is catalyzed by glutathione transferases

2. The Spontaneous and Glutathione S-Transferase-Mediated Reaction of Chlorambucil with Glutathione

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