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  • Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors.

Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors.

Steroids (2007-09-22)
Vânia M A Moreira, Tadas S Vasaitis, Vincent C O Njar, Jorge A R Salvador
ABSTRACT

A series of novel 1H- and 2H-indazole derivatives of the commercially available dehydroepiandrosterone acetate have been synthesized and tested for inhibition of human cytochrome 17alpha-hydroxylase-C(17,20)-lyase (CYP17), androgen receptor (AR) binding affinity, and cytotoxic potential against three prostate cancer (PC) cell lines.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Dehydroisoandrosterone 3-acetate, 97%