Trimetrexate: a new antifol entering clinical trials

Invest New Drugs. 1985;3(1):71-5. doi: 10.1007/BF00176828.

Abstract

Trimetrexate, a 2,4-diaminoquinazoline derivative, is a new antifol recently introduced into clinical trials. It differs from methotrexate principally in its transport (not carrier-mediated), and its intracellular retention (not polyglutamylated). Trimetrexate is active against tumors which are methotrexate-resistant on the basis of impaired transport, and has a broader range of antitumor activity in preclinical models. Animal studies predict toxicity principally to the central nervous system, gastrointestinal tract and bone marrow.

Publication types

  • Clinical Trial

MeSH terms

  • Animals
  • Biological Availability
  • Biological Transport
  • Cells, Cultured
  • Clinical Trials as Topic
  • DNA / biosynthesis
  • Dogs
  • Drug Evaluation, Preclinical
  • Folic Acid Antagonists / metabolism
  • Folic Acid Antagonists / pharmacology*
  • Folic Acid Antagonists / toxicity
  • Mice
  • Neoplasms, Experimental / drug therapy
  • Nucleosides / metabolism
  • Quinazolines / metabolism
  • Quinazolines / pharmacology*
  • Quinazolines / toxicity
  • Trimetrexate

Substances

  • Folic Acid Antagonists
  • Nucleosides
  • Quinazolines
  • DNA
  • Trimetrexate