CAS NO: | 614749-78-9 |
生物活性 | SM 16 is aALK5/ALK4kinase inhibitor withKis of 10 and 1.5 nM, respectively. | ||||||||||||||||
IC50& Target | Ki: ALK5 (10 nM), ALK4 (1.5 nM)[1] | ||||||||||||||||
体外研究 (In Vitro) | SM 16 inhibits TGFβ-induced plasminogen activator inhibitor-luciferase activity (IC50=64 nM) and TGFβ- or activin-induced Smad2 phosphorylation at concentrations between 100 and 620 nM. SM 16 is tested against >60 related and unrelated kinases and shows moderate off-target activity only against Raf (IC50=1 μM) and p38/SAPKa (IC50=0.8 μM). SM 16 exhibits no inhibitory activity against ALK family members ALK1 and ALK6[1]. | ||||||||||||||||
体内研究 (In Vivo) | SM 16 penetrates tumor cellsin vivo, suppressing tumor phosphorylated Smad2/3 levels for at least 3 h following treatment of tumor-bearing mice with a single i.p. bolus of 20 mg/kg SM 16. The growth of established AB12 tumors is significantly inhibited by 5 mg/kg/d SM 16 (P<0.001) delivered via s.c. miniosmotic pumps over 28 days[1]. | ||||||||||||||||
分子量 | 430.50 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H26N4O3 | ||||||||||||||||
CAS 号 | 614749-78-9 | ||||||||||||||||
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 : 65 mg/mL(150.99 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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