Synthesis and biological activities of a novel class of azole-containing antifungal agents

Bioorganic & Medicinal Chemistry Letters
1996.0

Abstract

A series of novel 1,2,3,4-tetrahydroisoquinoline derived azoles has been designed and synthesized as antifungal agents which might function as inhibitors of cytochrome P-450 dependent lanosterol 14ct-demethylase. In vitro tests showed that some of these compounds, especially 5b and 6b, effectively inhibit the growth of several strains of yeasts as well as molds.

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