Drug intelligence / Profile preview

Wuhan Univ. ERα/ARO compound 18c

Development stage
Preclinical
Lead developer
Wuhan University
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
01

Overview

Wuhan Univ. ERα/ARO compound 18c: sourced facts only. name: "Among them, compound 18c bifunctionally degrades and inhibits ERα/ARO, thus effectively suppressing the proliferation of MCF-7 cells while showing negligible cytotoxicity to normal cells."; target: "Among them, compound 18c bifunctionally degrades and inhibits ERα/ARO, thus effectively suppressing the proliferation of MCF-7 cells while showing negligible cytotoxicity to normal cells."; target: "Among them, compound 18c bifunctionally degrades and inhibits ERα/ARO, thus effectively suppressing the proliferation of MCF-7 cells while showing negligible cytotoxicity to normal cells."; developer: "Department of Hematology, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China."; modality: "Herein, we present a new category of dual-targeting PROTAC degraders designed to specifically target ERα and ARO."; stage: "In vivo, 18c promotes the degradation of ERα and ARO and inhibits the growth of MCF-7 xenograft tumors."

02

Targets

Source types: Peer-reviewed publication. Sources are available to Gosset users. Log in to see them.

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