Beng-Thong Ho

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 synthetase †‡

Analogs of Tetrahydrofolic Acid XXVII: Hydrophobic Bonding to Dihydrofolic Reductase by 2-Amino-4,6-disubstituted-5-alkylpyrimidines and 1-Alkyl-4,6-diamino-1,2-dihydro-s-triazines

Analogs of Tetrahydrofolic Acid XXXII:Hydrophobic Bonding to Dihydrofolic Reductase IV. Inhibition by p-Substituted Benzoic and Benzoyl-l-glutamic Acids

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‐triazines

Differential Inhibition of Dihydrofolic Reductase from Different Species

Analogs of tetrahydrofolic acid. XIII. On the mode of binding of the anilino group of 2-amino-5-(3-anilinopropyl)-6-methyl-4-pyrimidinol to dihydrofolic reductase and thymidylate synthetase †‡

Analogs of tetrahydrofolic acid XXXV: Hydrophobic bonding to dihydrofolic reductase VII. Species differences with substituted 4,6-diamino-1,2-dihydro-s-triazines

Analogs of tetrahydrofolic acid XXXIII. Hydrophobic bonding to dihydrofolic reductase V. Inhibition by some pyrimidines bridged to benzoic acid

Analogs of Tetrahydrofolic Acid XV: Mode of Binding of 2,4-Diaminopyrimidines to Folic Reductase and Thymidylate Synthetase

Analogs of tetrahydrofolic acid. XXIII. 1-(ω-phenylalkyl)-4,6-diamino-1,2-dihydro-s-triazines as inhibitors of dihydrofolic reductase†‡