Carbocyclic Analogues of the Potent Cytidine Deaminase Inhibitor 1-(β-d-Ribofuranosyl)-1,2-dihydropyrimidin-2-one (Zebularine)-Reference-Cited by-同舟云学术

Carbocyclic Analogues of the Potent Cytidine Deaminase Inhibitor 1-(β-d-Ribofuranosyl)-1,2-dihydropyrimidin-2-one (Zebularine)

Published:1998-06-16 Issue:14 Volume:41 Page:2572-2578
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Jeong Lak Shin¹,Buenger Greg¹,McCormack John J.¹,Cooney David A.¹,Hao Zhang¹,Marquez Victor E.¹

Affiliation:

1. Laboratory of Medicinal Chemistry, Division of Basic Sciences, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, and Department of Pharmacology, College of Medicine, and Vermont Regional Cancer Center, University of Vermont, Burlington, Vermont 05401

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm980111x

Reference39 articles.

1. Inhibition of cytidine deaminase by 2-oxopyrimidine riboside and related compounds

2. Potent inhibitors for the deamination of cytosine arabinoside and 5-aza-2?-deoxycytidine by human cytidine deaminase

3. Cytidine Deaminase. The 2·3 Å Crystal Structure of an Enzyme: Transition-state Analog Complex

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