
Journal of Medicinal Chemistry p. 3660 - 3668 (1995)
Update date:2022-08-02
Topics:
Gangjee
Zaveri
Kothare
Queener
Twenty 6-substituted 2,4-diaminotetrahydroquinazolines were designed, synthesized, and biologically evaluated as novel nonclassical inhibitors of dihydrofolate reductase (DHFR) from Pneumocystis carinii and Toxoplasma gondii and as antitumor agents. The 6
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