Drug intelligence / Profile preview

onalespib

Development stage
Phase 2
Lead developer
Astex Pharmaceuticals
Modality
Small Molecules
Administration
Intravenous
01

Overview

Onalespib is a synthetic, orally bioavailable small-molecule inhibitor of heat shock protein 90 (HSP90), a molecular chaperone involved in the maturation and stabilization of various client proteins critical for cell cycle control and signal transduction. By inhibiting HSP90, onalespib disrupts the function of multiple oncogenic proteins, leading to antineoplastic effects. It has been investigated primarily as an anticancer agent in several solid tumors, including non-small cell lung cancer, triple-negative breast cancer, prostate cancer, and glioblastoma. Onalespib was originally developed by Astex Therapeutics and further developed by Astex Pharmaceuticals (a subsidiary of Otsuka) and the National Cancer Institute[2][5][6][9].

Other names
AT13387AT-13387AT 13387onalespib
02

Targets

TRAP1 (Tumor necrosis factor receptor-associated protein 1)HSP90AB1 (Heat shock protein HSP 90-beta)HSP90AA1 (Heat shock protein HSP90-alpha)HSP90B1 (GRP94)

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