Drug intelligence / Profile preview

CCG-1423

Development stage
Preclinical
Lead developer
Kyoto University
Modality
Small Molecules
Administration
Intravitreal, Intraperitoneal, Oral
01

Overview

CCG-1423 is a small-molecule inhibitor of the Rho/MRTF/SRF transcriptional signaling pathway. Originally developed by Kyoto University, it functions by inhibiting Serum Response Factor (SRF)-mediated transcription, which is critical for the expression of genes involved in cell proliferation, migration, and myofibroblast differentiation. The compound has been shown to bind directly to Pirin, an iron-dependent cotranscription factor, which is essential for its inhibitory activity. In preclinical studies, CCG-1423 has demonstrated efficacy in models of melanoma, prostate cancer, cardiac fibrosis, and atherosclerosis. It is widely used as a research tool to study Rho-dependent signaling but has not yet entered clinical trials.

02

Targets

PIR (Pirin)MICAL2 (Microtubule associated monooxygenase, calponin and LIM domain containing 2)TIRAP (TIRAP / MAL)MRTFA (Myocardin-related transcription factor A)

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