SAR131675 (b)
CAS No. 1092539-44-0
SAR131675 (b) ( SAR131675 | SAR 131675 | SAR-131675 )
产品货号. M17805 CAS No. 1092539-44-0
SAR131675 是一种有效且特异性的 VEGFR-3 抑制剂。它分别抑制 HEK 细胞中的 VEGFR-3 酪氨酸激酶活性 (IC50: 20 nmol/L) 和 VEGFR-3 自磷酸化 (IC50: 45 nmol/L)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥252 | 有现货 |
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| 10MG | ¥370 | 有现货 |
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| 25MG | ¥597 | 有现货 |
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| 50MG | ¥898 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称SAR131675 (b)
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SAR131675 是一种有效且特异性的 VEGFR-3 抑制剂。它分别抑制 HEK 细胞中的 VEGFR-3 酪氨酸激酶活性 (IC50: 20 nmol/L) 和 VEGFR-3 自磷酸化 (IC50: 45 nmol/L)。
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产品描述SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine kinase activity and VEGFR-3 autophosphorylation in HEK cells with IC(50) values of 20 and 45 nmol/L, respectively. SAR131675 was found to be highly selective for VEGFR-3 versus 107 receptors, enzymes, ion channels, and 65 kinases. SAR131675 is the first highly specific VEGFR-3-TK inhibitor described to date, displaying significant antitumoral and antimetastatic activities in vivo through inhibition of lymphangiogenesis and TAM invasion.
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体外实验SAR131675 is a potent and selective VEGFR3 inhibitor with an IC50 of 23 nM.
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体内实验——
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同义词SAR131675 | SAR 131675 | SAR-131675
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通路Others
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靶点Other Targets
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受体VEGFR3
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研究领域Cancer
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适应症——
化学信息
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CAS Number1092539-44-0
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分子量358.16
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分子式C18H22N4O4
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纯度>98% (HPLC)
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溶解度——
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SMILESCCn1c(c(c(=O)c2c1nc(cc2)C#CC(C)(COC)O)C(=O)NC)N
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化学全称2-amino-1-ethyl-7-(3-hydroxy-4-methoxy-3-methylbut-1-yn-1-yl)-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Yu J, et al. Biochem Biophys Res Commun. 2016 Mar 25;472(1):182-8.
产品手册
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