Inhibition of uridine phosphorylase: synthesis and structure-activity relationships of aryl-substituted 5-benzyluracils and 1-[(2-hydroxyethoxy)methyl]-5-benzyluracils.-Reference-Cited by-同舟云学术

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Inhibition of uridine phosphorylase: synthesis and structure-activity relationships of aryl-substituted 5-benzyluracils and 1-[(2-hydroxyethoxy)methyl]-5-benzyluracils.

Published:1995-09 Issue:19 Volume:38 Page:3850-3856
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Orr G. Faye,Musso David L.,Boswell G. Evan,Kelley James L.,Joyner Suzanne S.,Davis Stephen T.,Baccanari David P.

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm00019a015

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Cytotoxicity Studies of 5-Arylaminouracil Derivatives;Molecular Biology;2024-04

2. Design and synthesis of 4-piperazinyl quinoline derived urea/thioureas for anti-breast cancer activity by a hybrid pharmacophore approach;Journal of Enzyme Inhibition and Medicinal Chemistry;2019-01-01

3. Flexible Nucleobase Analogues: Novel Tools for Exploring Nucleic Acids;Chemical Biology of Nucleic Acids;2014

4. Synthesis of Novel 2-(Substituted amino)alkylthiopyrimidin-4(3H)-ones as Potential Antimicrobial Agents;Molecules;2013-12-27

5. Exploring new inhibitors of Plasmodium falciparum purine nucleoside phosphorylase;European Journal of Medicinal Chemistry;2010-11

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