N10-substituted 5,8-dideazafolate inhibitors of glycinamide ribonucleotide transformylase

J Med Chem. 1987 Jul;30(7):1254-6. doi: 10.1021/jm00390a024.

Abstract

A series of 5,8-dideazafolates bearing ethyl, isopropyl, cyclopropylmethyl, propargyl, 3-cyanopropyl, carboxymethyl, 2-carboxyethyl, phenacyl, 3-fluorobenzyl, and 5-uracilylmethyl substituents at N10 were tested as inhibitors of purified L5178Y glycinamide ribonucleotide transformylase (GAR TFase), which requires 10-formyltetrahydrofolate as cofactor. All of these cofactor analogues exhibited competitive inhibition against N10-formyl-5,8-dideazafolate, with Ki's ranging from 2 to 32 microM.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acyltransferases / antagonists & inhibitors*
  • Folic Acid / analogs & derivatives*
  • Hydroxymethyl and Formyl Transferases*
  • Phosphoribosylglycinamide Formyltransferase
  • Structure-Activity Relationship

Substances

  • Folic Acid
  • Hydroxymethyl and Formyl Transferases
  • Phosphoribosylglycinamide Formyltransferase
  • Acyltransferases