CAS NO: | 694433-59-5 |
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 | SB-505124 is a selective inhibitor of TGF-β Receptortype I receptors(ALK4,ALK5,ALK7), with IC50s of 129 nM and 47 nM for ALK4,ALK5, respectively, but it does not inhibitALK1, 2, 3, or 6. | ||||||||||||||||
IC50& Target | IC50: 129 nM (ALK4), 47 nM (ALK5) | ||||||||||||||||
体外研究 (In Vitro) | SB-505124 demonstrates no toxicity to renal epithelial A498 cells at concentrations up to 100 μM for 48 h. 505124 inhibits the closely related ALK4 with an IC50value of 129±11 nM (about 2.5-fold less sensitive than ALK5) but does not inhibit ALK2 at concentrations up to 10 μM. SB-505124 (1 μM) inhibits the TGF-β-induced phosphorylation of Smad2 in all three of these cell lines in a concentration-dependent fashion. SB-505124 (1 or 5 μM) potently inhibits TGF-β-induced activation of JNK/SAP, extracellular signal-regulated kinase 1/2, and p38 despite the different patterns of activation in these cells[1]. SB-505124 (10 μM) impairs Smad2 phosphorylation and CTGF and α-SMA expression in vitro[2]. SB-505124 susspresses CTGF and α-SMA observed by immunofluorescence. Cell outgrowth from explants dissected from eyes to which SB-505124 is applied during GFS is robust while outgrowth is poor from those treated with MMC[3]. | ||||||||||||||||
体内研究 (In Vivo) | SB-505124 (5 mg/kg; i.p.) alone has no effect in C57Bl6 mice with A549 xenografts, but administration of SB-505124 with a single dose of Carboplatin (60 mg/kg) results in durable responses without the need for maintenance therapy in five animals[4].
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分子量 | 335.40 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H21N3O2 | ||||||||||||||||
CAS 号 | 694433-59-5 | ||||||||||||||||
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 : 113.33 mg/mL(337.90 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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