Irreversible enzyme inhibitors. CLVIII. Effect of bridge modification on the selective irreversible inhibition of a dihydrofolic reductase from L1210 mouse leukemia and liver by 2,4-diamino-5-(3,4-dichlorophenyl)-6-[p-[m-(fluorosulfonyl)benzamidomethyl]phenoxymethyl]pyrimidine. II
Author:
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm00304a028
Cited by 7 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. Repositioning of DHFR Inhibitors;Current Topics in Medicinal Chemistry;2016-05-30
2. Structure-activity relationships of dihydrofolated reductase inhibitors;Chemical Reviews;1984-08-01
3. Formulation of De Novo Substituent Constants in Correlation Analysis: Inhibition of Dihydrofolate Reductase by 2,4‐Diamino‐5‐ (3,4‐dichlorophenyl)‐6‐substituted Pyrimidines;Journal of Pharmaceutical Sciences;1975-07
4. Irreversible enzyme inhibitors. CLXXV. Irreversible inhibition of purifed dihydrofolic reductase;Journal of Medicinal Chemistry;1970-11
5. Irreversible enzyme inhibitors. CLXVI. Active-site-directed irreversible inhibitors of dihydrofolic reductase derived from 2,4-diamino-5-(3,4-dichlorophenyl)pyrimidine with 6 substituents and some factors in their cell wall transport;Journal of Medicinal Chemistry;1970-01
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