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- SD-208 627536-09-8

- SD-208 627536-09-8
SD-208 627536-09-8
产品描述 描述 SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, >100-fold selectivity over TGF-βRII.
纯度 >98%储存/保存方法 Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.基本信息 别名 SD 208;SD208;TGF-β RI Kinase Inhibitor V外观 off-white to tan solid可溶性/溶解性 DMSO : 7.1 mg/mL (20 mM), with gentle warming生物活性 靶点 TGF-βRI (ALK5)In vitro(体外研究) SD-208 inhibits the cell growth and constitutive and TGF-beta-evoked migration and invasion, and enhances immunogenicity in murine SMA-560 and human LN-308 glioma cells. SD-208 blocka TGF-beta-induced phosphorylation of the receptor-associated Smads, Smad2 and Smad3, and stimulates epithelial-to-mesenchymal transdifferentiation, migration, and invasiveness into Matrigel in vitro. SD-208 also abolishes the promoting effect of TGF-β on neointimal smooth muscle-like cell (SMLC) proliferation and migration in vitro.In vivo(体内研究) SD-208 (1 mg/mL, p.o.) significantly prolongs the median survival of SMA-560 glioma-bearing mice. In syngeneic 129S1 mice, SD-208 (60 mg/kg/d, p.o.) inhibits primary R3T tumor growth, and reduces the number and the size of lung metastases. In the murine aortic allograft model, SD-208 effectively reduces the formation of intimal hyperplasia of transplant arteriosclerosis (TA).参考文献 参考文献 研究领域 研究领域 CancerCancer MetabolismCancerTumor biomarkersDrug DiscoverySmall Molecule DrugLead Compound DiscoverySD-208 627536-09-8温馨提示:本产品仅作科研实验使用,不支持临床等研究
