Comparison of biochemical parameters of benzamide riboside, a new inhibitor of IMP dehydrogenase, with tiazofurin and selenazofurin-Reference-Cited by-同舟云学术

Comparison of biochemical parameters of benzamide riboside, a new inhibitor of IMP dehydrogenase, with tiazofurin and selenazofurin

Published:1994-10 Issue:7 Volume:48 Page:1413-1419
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Gharehbaghi Kamran,Sreenath Ajay,Hao Zhang,Paull Kenneth D.,Szekeres Thomas,Cooney David A.,Krohn Karsten,Jayaram Hiremagalur N.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference23 articles.

1. Initial studies on the mechanism of action of a new oncolytic thiazole nucleoside, 2-β-D-ribofuranosylthiazole-4-carboxamide;Jayaram;Biochem Pharmacol,1982

2. Conversion of 2-β-D-ribofuranosyl-selenazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase inhibitory properties;Jayaram;Biochem Pharmacol,1983

3. Studies on the mechanism of action of 2-β-D-ribofuranosylthizole-4-carboxamide. V. Factors governing the response of murine tumors to tiazofurin;Ahluwalia;Drug Metab Dispos,1984

4. Relationship between the cytotoxicity and tiazofurin and its metabolism by cultured human lung cancer cells;Carney;J Clin Invest,1985

5. Cytotoxicity of a new IMP dehydrogynase inhibitor, benzamide riboside, to human myelogenous leukemia K562 cells;Jayaram;Biochem Biophys Res Commun,1992

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