Conversion of 2-β-D-ribofuranosylselenazole-4-carboxamide to an analogue of nad with potent imp dehydrogenase-inhibitory properties-Reference-Cited by-同舟云学术

Conversion of 2-β-D-ribofuranosylselenazole-4-carboxamide to an analogue of nad with potent imp dehydrogenase-inhibitory properties

Published:1983-09 Issue:17 Volume:32 Page:2633-2636
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Jayaram Hiremagalur N.,Ahluwalia Gurpreet S.,Dion Robert L.,Gebeyehu Gulilat,Marquez Victor E.,Kelley James A.,Robins Roland K.,Cooney David A.,Johns David G.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference11 articles.

1. The invitro inhibition of purine nucleotide biosynthesis by 2-β-D-ribofuranosylthiazole-4-carboxamide

2. Studies on the mechanism of action of 2-β-d-ribofuranosylthiazole-4-carboxamide (NSC 286193)-II

3. The conversion of 2-β-D-ribofuranosylthiazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase-inhibitory properties

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