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CCG-203971

Chemical Structure : CCG-203971

CAS No.: 1443437-74-8

CCG-203971 (CCG203971)

Catalog No.: PC-62825Not For Human Use, Lab Use Only.

CCG-203971(CCG203971) is a potent Rho/MKL1/SRF transcriptional pathway inhibitor, suppresses PC-3 cell migration in scratch wound assays (IC50=4.2 uM), blocks nuclear localization and activity of MRTF-A in SK-Mel-147 cells.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

CCG-203971 (CCG203971) is a potent Rho/MKL1/SRF transcriptional pathway inhibitor, suppresses PC-3 cell migration in scratch wound assays (IC50=4.2 uM), blocks nuclear localization and activity of MRTF-A in SK-Mel-147 cells.
CCG-203971 selectively inhibits proliferation of SSc-derived dermal fibroblasts but not that of normal fibroblasts.
CCG-203971 inhibits expression of CTGF, α-SMA, and COL1A2 in SSc fibroblasts as well as in LPA and in TGFβ-stimulated fibroblasts.
CCG-203971 prevents bleomycin-induced skin thickening and collagen deposition in vivo.

Physicochemical Properties

M.Wt 408.88
Formula C23H21ClN2O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-(4-chlorophenyl)-1-[3-(2-furanyl)benzoyl]-3-piperidinecarboxamide

References

1. Bell JL, et al. Bioorg Med Chem Lett. 2013 Jul 1;23(13):3826-32.

2. Haak AJ, et al. J Pharmacol Exp Ther. 2014 Jun;349(3):480-6.

3. Haak AJ, et al. Mol Cancer Ther. 2017 Jan;16(1):193-204.

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