SGX-523

产品编号: DC7294
SGX-523
结构式
1022150-57-7
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中国地区超过5000个高品质化合物库存
应用领域
SGX-523 is a selective Met inhibitor with IC50 of 4 nM, no activity to BRAFV599E, c-Raf, Abl and p38α.
Cas No.: 1022150-57-7
名称: 6-(6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-ylthio)quinoline
别名: SGX523; SGX 523
SMILES: CN1N=CC(C2=NN3C(SC4=CC5=C(N=CC=C5)C=C4)=NN=C3C=C2)=C1
分子式: C18H13N7S
分子量: 359.41
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: SGX-523 belongs to the class of c-Met/hepatocyte growth factor receptor (HGFR) tyrosine kinase inhibitors. SGX-523 stabilizes MET in a unique inactive con Formation that is inaccessible to other protein kinases, suggesting an explanation For its selectiv
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
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MSDS_3421_DC7294_1022150-57-7
COA
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产品编号 产品名称 应用领域
DC7294 SGX-523 SGX-523 is a selective Met inhibitor with IC50 of 4 nM, no activity to BRAFV599E, c-Raf, Abl and p38α.
DC7177 JNJ 38877605 JNJ-38877605 is an ATP-competitive inhibitor of c-Met with IC50 of 4 nM, 600-fold selective for c-Met than 200 other tyrosine and serine-threonine kinases.
DC7081 PF-04217903 PF-04217903 is a selective ATP-competitive c-Met inhibitor with IC50 of 4.8 nM, susceptible to oncogenic mutations (no activity to Y1230C mutant).