CCG 1423
Chemical Name: N-[2-[(4-Chlorophenyl)amino]-1-methyl-2-oxoethoxy]-3,5-bis(trifluoromethyl)benzamide
Purity: ≥99%
Biological Activity
CCG 1423 is a Rho/SRF pathway inhibitor; stimulates apoptosis of a melanoma cell line overexpressing RhoC (A375M2). Suppresses Rho-dependent invasion of PC-3 prostate cancer cells in vitro and inhibits lysophosphatidic acid-induced DNA synthesis in PC-3 prostate cancer cells. When used in combination with Retinoic acid, LY 294002 and Pyridone 6, it induces intermediate mesoderm differentiation from ESCs.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Combination of small molecules enhances differentiation of mouse embryonic stem cells into intermediate mesoderm through BMP7-positive cells.
Mae et al.
Biochem.Biophys.Res.Commun., 2010;393:877 -
CCG-1423: a small-molecule inhibitor of RhoA transcriptional signaling.
Evelyn et al.
Mol.Cancer Ther., 2007;6:2249
Product Datasheets
Citations for CCG 1423
The citations listed below are publications that use Tocris products. Selected citations for CCG 1423 include:
4 Citations: Showing 1 - 4
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Inhibitors of Venezuelan Equine Encephalitis Virus Identified Based on Host Interaction Partners of Viral Non-Structural Protein 3.
Authors: Aarthi Et al.
Viruses 2021;13
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Cell Type Dependent Suppression of Inflammatory Mediators by Myocardin Related Transcription Factors.
Authors: Li Et al.
Front Physiol 2021;12:732564
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Regulation of the Muscarinic M3 Receptor by Myocardin-Related Transcription Factors.
Authors: Li Et al.
Front Physiol 2021;12:710968
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Narciclasine, an isocarbostyril alkaloid, has preferential activity against primary effusion lymphoma.
Authors: Preet M Et al.
Sci Rep 2020;10:5712
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