Drug intelligence / Profile preview

BMS-193885

Development stage
Discontinued
Lead developer
Bristol Myers Squibb
Modality
Small Molecules
Administration
Intraperitoneal, Intravenous, Intracerebroventricular, Intrahypothalamic
01

Overview

BMS-193885 is a potent, selective, and competitive small molecule antagonist of the neuropeptide Y1 (NPY Y1) receptor, originally developed by Bristol Myers Squibb. It exhibits high affinity for the human Y1 receptor (Ki of 3.3 nM) with significant selectivity over other NPY receptor subtypes such as Y2, Y4, and Y5. Although the compound is brain-penetrant and demonstrated the ability to reduce food intake and body weight in animal models of obesity through central Y1 receptor inhibition, it lacks oral bioavailability. Consequently, BMS-193885 has primarily served as a pharmacological research tool and has not advanced into human clinical trials.

Other names
BMS-193885 L-Lactic acidBMS193885 L-Lactic acidBMS 193885 L-Lactic acidBMS-193885 lactateBMS193885 lactateBMS 193885 lactate
02

Targets

NPY1R (Neuropeptide Y receptor Y1)

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