High-affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size

J Med Chem. 1996 Feb 16;39(4):892-903. doi: 10.1021/jm9505122.

Abstract

A series of 7,8-dialkylpyrrolo[3,2-f]quinazolines were prepared as inhibitors of dihydrofolate reductase (DHFR). On the basis of an apparent inverse relationship between compound size and antifungal activity, the compounds were designed to be relatively small and compact. Inhibitor design was aided by GRID analysis of the three-dimensional structure of Candida albicans DHFR, which suggested that relatively small, branched alkyl groups at the 7- and 8-positions of the pyrroloquinazoline ring system would provide optimal interactions with a hydrophobic region of the protein. The compounds were potent inhibitors of fungal and human DHFR, with K(i) values as low as 7.1 and 0.1 pM, respectively, and were highly active against C. albicans and an array of tumor cell lines. In contrast to known lipophilic inhibitors of DHFR such as trimetrexate and piritrexim, members of this series of pyrroloquinazolines were not susceptible to P-glycoprotein-mediated multidrug resistance and also showed significant distribution into lung and brain tissue. The compounds were active in lung and brain tumor models and displayed in vivo activity against Pneumocystis carinii and C. albicans.

Publication types

  • Comparative Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / drug effects
  • Animals
  • Anti-Infective Agents / chemical synthesis*
  • Anti-Infective Agents / pharmacology*
  • Anti-Infective Agents / toxicity
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Brain Neoplasms / drug therapy
  • Candidiasis / drug therapy
  • Cell Division / drug effects
  • Cell Line
  • Crystallography, X-Ray
  • Drug Design
  • Drug Resistance, Multiple
  • Enzyme Inhibitors / chemical synthesis*
  • Enzyme Inhibitors / pharmacology
  • Folic Acid Antagonists / chemistry
  • Humans
  • Lung Neoplasms / drug therapy
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Mice
  • Mice, Nude
  • Mice, SCID
  • Models, Molecular
  • Molecular Conformation
  • Molecular Structure
  • Molecular Weight
  • Pneumonia, Pneumocystis / drug therapy
  • Protein Structure, Secondary
  • Quinazolines / chemical synthesis*
  • Quinazolines / pharmacology*
  • Quinazolines / toxicity
  • Structure-Activity Relationship
  • Toxoplasma / drug effects
  • Tumor Cells, Cultured

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Anti-Infective Agents
  • Antineoplastic Agents
  • Enzyme Inhibitors
  • Folic Acid Antagonists
  • Quinazolines