Drug intelligence / Profile preview

M64

Development stage
Preclinical
Lead developer
Northeast Ohio Medical University
Modality
Small Molecules
Administration
Oral, Topical, Intravenous, Intraperitoneal
01

Overview

M64 (often studied as its water-soluble hydrochloride salt, M64HCl) is a novel, selective, small-molecule focal adhesion kinase (FAK) activator. Developed through structure-activity relationship (SAR) studies as a third-generation derivative of ZINC40099027, M64 directly interacts with the FAK kinase domain to stimulate FAK autophosphorylation (specifically at Tyr397) and downstream ERK1/2 signaling. This activation promotes epithelial sheet migration, cell motility, and angiogenesis. M64 is being investigated for its therapeutic potential in promoting gastrointestinal mucosal wound healing (such as in nonsteroidal anti-inflammatory drug [NSAID]-induced enteropathy, ischemic jejunal ulcers, and inflammatory bowel disease [IBD]), accelerating skin wound repair, and managing high bone mass disorders by promoting osteoclastogenesis and bone resorption.

Other names
1-(2-(dimethylamino)-2-(pyridin-4-yl)ethyl)-3-(2-morpholino-5-(trifluoromethyl)phenyl)urea1-(2-(dimethylamino)-2-(pyridin-4-yl)ethyl)-3-(2-morpholino-5-(trifluoromethyl)phenyl)urea hydrochlorideM64 hydrochlorideM-64 hydrochlorideM 64 hydrochloride
02

Targets

FAK (Focal adhesion kinase)

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