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 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 |
| 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) |
| InChIKey | HERLZBNILRVHQN-UHFFFAOYSA-N |
| SMILES | ClC(C=C1)=CC=C1NC(C(C2)CCCN2C(C3=CC(C4=CC=CO4)=CC=C3)=O)=O |
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 Germany | WGK 3 |
|---|---|
| 存储类别 | 11 - 可燃固体 |
| 危险性类别 | 急性毒性 类别4 经口 |
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2026/06/05 | HY-108361 | CCG-203971 | 1443437-74-8 | 5 mg | 330元 |
| 2026/06/05 | HY-108361 | 1443437-74-8 CCG-203971 | 1443437-74-8 | 10mM * 1mLin DMSO | 363元 |
