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CCG-203971

SIGMA/SML1422 - ≥98% (HPLC)

Synonym: N-(4-Chlorophenyl)-1-[3-(2-furanyl)benzoyl]-3-piperidinecarboxamide

CAS Number: 1443437-74-8
Empirical Formula (Hill Notation): C23H21ClN2O3
Molecular Weight: 408.88
MDL Number: MFCD28166491
Linear Formula: C23H21ClN2O3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML1422-5MG 5 mg
$78.00
1/EA
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45-SML1422-25MG 25 mg
$318.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
InChI 1S/C23H21ClN2O3/c24-19-8-10-20(11-9-19)25-22(27)18-6-2-12-26(15-18)23(28)17-5-1-4-16(14-17)21-7-3-13-29-21/h1,3-5,7-11,13-14,18H,2,6,12,15H2,(H,25,27)
InChI key HERLZBNILRVHQN-UHFFFAOYSA-N
Quality Level 100 
SMILES string ClC(C=C1)=CC=C1NC(C(C2)CCCN2C(C3=CC(C4=CC=CO4)=CC=C3)=O)=O
storage temp. 2-8°C
Biochem/physiol Actions: CCG-203971 is an inhibitor of the Rho/MKL1/SRF transcriptional pathway, which has been shown to play a role in metastasis of melanoma and breast cancer and clinically associated with castration-resistant prostate cancer. CCG-203971 is a second-generation analog of CCG-1423 (SML0987) with an IC50 of 4.2 μM vs 1 μM for CCG-1423, but less cytotoxicity. In mouse studies, CCG-203971 inhibited invasion of PC-3 prostate cancer cells and was well tolerated up to doses of 100 mg/kg IP over 5 days.

The Rho/MRTF/SRF pathway has also been shown to be involved in multiple types of solid organ fibrosis. CCG-203971 repressed both matrix-stiffness and TGF-β-mediated fibrogenesis in human colonic myofibroblasts and showed antifibrotic activity in a murine model of skin injury and in pulmonary fibrosis lung fibroblasts.
Biochem/physiol Actions: CCG-203971 is an inhibitor of the Rho/MKL1/SRF transcriptional pathway.
Packaging: 5, 25 mg in glass bottle
Symbol GHS07  GHS07
Signal word Warning
Hazard statements H302
Precautionary statements P301 + P312 + P330
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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