Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA059612-01A2
Application #
2100208
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Project Start
1996-04-02
Project End
1999-03-31
Budget Start
1996-04-02
Budget End
1997-03-31
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Chemistry
Type
Schools of Medicine
DUNS #
003255213
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Zheng, Zhe-Bin; Zhu, Guozhang; Tak, Heekyung et al. (2005) N-(2-hydroxypropyl)methacrylamide copolymers of a glutathione (GSH)-activated glyoxalase i inhibitor and DNA alkylating agent: synthesis, reaction kinetics with GSH, and in vitro antitumor activities. Bioconjug Chem 16:598-607
Joseph, Erin; Ganem, Bruce; Eiseman, Julie L et al. (2005) Selective inhibition of MCF-7(piGST) breast tumors using glutathione transferase-derived 2-methylene-cycloalkenones. J Med Chem 48:6549-52
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Hamilton, Diana S; Zhang, Xiyun; Ding, Zhebo et al. (2003) Mechanism of the glutathione transferase-catalyzed conversion of antitumor 2-crotonyloxymethyl-2-cycloalkenones to GSH adducts. J Am Chem Soc 125:15049-58
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Sharkey, E M; O'Neill, H B; Kavarana, M J et al. (2000) Pharmacokinetics and antitumor properties in tumor-bearing mice of an enediol analogue inhibitor of glyoxalase I. Cancer Chemother Pharmacol 46:156-66
Kavarana, M J; Kovaleva, E G; Creighton, D J et al. (1999) Mechanism-based competitive inhibitors of glyoxalase I: intracellular delivery, in vitro antitumor activities, and stabilities in human serum and mouse serum. J Med Chem 42:221-8

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