CAS NO: | 627536-09-8 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | SD-208 is a selective TGF-βRI (ALK5) inhibitor with IC50 of 48 nM, and >100-fold selectivity over TGF-βRII. | ||||||||||||||||
IC50& Target | IC50: 48 nM (TGF-βRI) | ||||||||||||||||
体外研究 (In Vitro) | 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[1]. SD-208 blocks 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[2]. SD-208 also abolishes the promoting effect of TGF-β on neointimal smooth muscle-like cell (SMLC) proliferation and migration in vitro[3]. | ||||||||||||||||
体内研究 (In Vivo) | SD-208 (1 mg/mL, p.o.) significantly prolongs the median survival of SMA-560 glioma-bearing mice[1]. 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[2]. In the murine aortic allograft model, SD-208 effectively reduces the formation of intimal hyperplasia of transplant arteriosclerosis (TA)[3]. | ||||||||||||||||
分子量 | 352.75 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H10ClFN6 | ||||||||||||||||
CAS 号 | 627536-09-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 9.09 mg/mL(25.77 mM;Need ultrasonic) 配制储备液
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