Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition-Reference-Cited by-同舟云学术

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Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition

Published:1999-06 Issue:11 Volume:9 Page:1477-1480
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Guerin David J.,Mazeas Daniel,Musale Manoj S.,Naguib Fardos N.M.,Al Safarjalani Omar N.,el Kouni Mahmoud H.,Panzica Raymond P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference6 articles.

1. Synthesis of a new class of uridine phosphorylase inhibitors

2. 5-Benzylbarbituric acid derivatives, potent and specific inhibitors of uridine phosphorylase

3. Structure-activity relationship of ligands of the pyrimidine nucleoside phosphorylases

4. Preparation of 5-substituted benzylbarburituric acids and investigation of the effect of the benzyl and substituted benzyl groups on the acidity of barbituric acid

5. Substituent and solvent effects on tautomeric equilibria of barbituric acid derivatives and isoterically related compounds

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3. Synthesis and Herbicidal Activity of 5-(1-Amino-2-phenoxyethylidene)barbituric Acid Derivatives;Chinese Journal of Organic Chemistry;2021

4. Bentonite Catalyzed an Efficient and Green Synthesis of Arylidene Meldrum's Acid Derivatives in Aqueous Media;Letters in Organic Chemistry;2020-08-07

5. Synthesis and antitumor activity of some nitrogen heterocycles bearing pyrimidine moiety;Journal of Heterocyclic Chemistry;2020-07-19

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