Irreversible Enzyme Inhibitors LXX
- 1 January 1967
- journal article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 56 (1) , 28-32
- https://doi.org/10.1002/jps.2600560105
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Analogs of Tetrahydrofolic Acid XXXIIJournal of Pharmaceutical Sciences, 1966
- Analogs of tetrahydrofolic acid. XXXI. Hydrophobic bonding to dihydrofolic reductase. III. Further observations on conformational aspects of hydrophobic bonding with some 5‐alkyl‐2,4‐diamino‐6‐pyrimidinolsJournal of Heterocyclic Chemistry, 1965
- Analogs of tetrahydrofolic acid. XXIX. Hydrophobic bonding to dihydrofolic reductase. II. On the mode of phenyl binding of 1‐aryl‐4,6‐diamino‐1,2‐dihydro‐2,2‐dimethyl‐s‐triazinesJournal of Heterocyclic Chemistry, 1965
- Analogs of Tetrahydrofolic Acid XXVIIIJournal of Pharmaceutical Sciences, 1965
- Analogs of Tetrahydrofolic Acid XXVIIJournal of Pharmaceutical Sciences, 1965
- Analogs of tetrahydrofolic acid. XXI. Synthesis of 6‐bromomethyl‐5‐(p‐chlorophenyl)‐2,4‐diaminopyrimidine and its evaluation as a dihydrofolic reductase inhibitorJournal of Heterocyclic Chemistry, 1965
- Differential Inhibition of Dihydrofolic Reductase from Different SpeciesJournal of Pharmaceutical Sciences, 1964
- Nonclassical Antimetabolites XV.Journal of Pharmaceutical Sciences, 1964
- Factors in the Design of Active-Site-Directed Irreversible InhibitorsJournal of Pharmaceutical Sciences, 1964
- Analogs of tetrahydrofolic acid. XII. On the relative contribution by the 2‐amino and 4‐hydroxy groups of 2‐amino‐5‐(3‐anilinopropyl)‐6‐methyl‐4‐pyrimidinol to inhibition of folic reductase and thymidylate synthetaseJournal of Heterocyclic Chemistry, 1964