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2-(2-bromophenylamino)-5-(3-fluorophenyl)-1,3,4-thiadiazole

Development stage
Preclinical
Modality
Small Molecules
01

Overview

2-(2-bromophenylamino)-5-(3-fluorophenyl)-1,3,4-thiadiazole (Compound B3) is a synthetic small molecule and a nonsteroidal aromatase inhibitor. It features a 1,3,4-thiadiazole scaffold substituted with 2-bromophenylamino and 3-fluorophenyl groups. In preclinical studies, the compound demonstrated selective cytotoxicity against estrogen-dependent breast cancer cell lines (MCF-7) compared to estrogen-independent lines (MDA-MB-231), suggesting its potential for treating hormone-responsive malignancies. Molecular modeling and dynamics simulations indicate that it binds to the active site of the aromatase enzyme in a manner similar to native inhibitors, effectively blocking the biosynthesis of estrogen.

Other names
N-(2-bromophenyl)-5-(3-fluorophenyl)-1,3,4-thiadiazol-2-amineCompound B3
02

Targets

CYP19A1 (Aromatase)

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