1443437-74-8

1443437-74-8

中文名称1443437-74-8
中文同义词化合物CCG203971;N-(4-氯苯基)-1-(3-(2-呋喃基)苯甲酰基)-3-哌啶甲酰胺;CCG 203971,抑制MRTF / SRF基因转录通路;PERFEMIKER]CCG-203971,98%;化合物CCG203971,10 MM DMSO 溶液;1443437-74-8;CCG 203971;CCG 203971【CAS:1443437-74-8】【规格:1ml】【纯度:10mM in DMSO】;CCG 203971【CAS:1443437-74-8】【规格:1ml】【纯度:10mM in DMSO】
英文名称CCG-203971
英文同义词CCG-203971;CCG 203971;CCG203971;CCG-203971;N-(4-Chlorophenyl)-1-[3-(2-furanyl)benzoyl]-3-piperidinecarboxamide;N-(4-chlorophenyl)-1-[3-(furan-2-yl)benzoyl]piperidine-3-carboxamide;203971;3-Piperidinecarboxamide, N-(4-chlorophenyl)-1-[3-(2-furanyl)benzoyl]-;Rho,Ras,Inhibitor,SRF,CCG 203971,CCG-203971,MKL1,inhibit,MRTF,anti-metastasis,PC-3,migration;CC 203971
CAS号1443437-74-8
分子式C23H21ClN2O3
分子量408.88
EINECS号
相关类别抑制剂
Mol文件1443437-74-8.mol
结构式1443437-74-8 结构式

1443437-74-8 性质

沸点656.0±55.0 °C(Predicted)
密度1.305±0.06 g/cm3(Predicted)
储存条件2-8°C
溶解度DMSO:81.0(最大浓度 mg/mL);198.1(最大浓度 mM)
形态粉末
酸度系数(pKa)13.69±0.70(Predicted)
颜色白色至米色
InChI1S/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)
InChIKeyHERLZBNILRVHQN-UHFFFAOYSA-N
SMILESClC(C=C1)=CC=C1NC(C(C2)CCCN2C(C3=CC(C4=CC=CO4)=CC=C3)=O)=O

1443437-74-8 用途与合成方法

CCG-203971 是第二代 Rho/MRTF/SRF 通路抑制剂。CCG-203971 有效靶向 RhoA/C 激活的 SRE 荧光素酶 (IC50=6.4 μM)。CCG-203971 抑制 PC-3 细胞迁移,IC50 为 4.2 μM。CCG-203971 具有潜在的抗转移作用。

RhoA/MRTF-A

CCG-203971, a second-generation Ras homolog gene family, member A (RhoA)/myocardin-related transcription factor A (MRTF-A)/serum response factor (SRF) pathway inhibitor, represses both matrix-stiffness and transforming growth factor beta–mediated fibrogenesis as determined by protein and gene expression in a dose-dependent manner. CCG-203971 significantly represses TGF-β- induced MKL1 expression at 25 μM concentration. Human dermal fibroblasts are plated onto 96-well plates and allowed to grow for 3 days in the presence of 30 μM CCG-203971 or DMSO vehicle. Viable cell density is assessed through enzymatic reduction of the water-soluble tetrazolium dye WST-1. Scleroderma dermal fibroblasts proliferate faster than normal cells, and this is inhibited by CCG-203971.

CCG-203971 is tested in a Bleomycin skin injury model. Bleomycin is administered in 50 μL of DMSO intraperitoneally. Preliminary studies show that Bleomycin administered in this manner is well tolerated at 100 mg/kg twice a day. Intradermal Bleomycin for 2 weeks along with the DMSO control (50 μL i.p.) results in marked dermal thickening (P<0.0001) compared with the PBS+DMSO group, which does not receive Bleomycin. CCG-203971 treatment strongly and significantly (P<0.001) suppresses the Bleomycin-induced skin thickening in this model. Skin collagen amounts, assessed by measurement of hydroxyproline content, show similar results. Bleomycin injections promote collagen deposition (P<0.01) and CCG-203971 is able to block this effect (P<0.05).

安全信息

WGK GermanyWGK 3
存储类别11 - 可燃固体
危险性类别急性毒性 类别4 经口

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2026/06/05HY-108361CCG-2039711443437-74-85 mg330元
2026/06/05HY-1083611443437-74-8
CCG-203971
1443437-74-810mM * 1mLin DMSO363元

1443437-74-8 上下游产品信息

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