Glumetinib, also known as SCC244, is a novel, potent and highly selective inhibitor of c-Met in MET-dependent cancer models. SCC244 showed subnanomolar potency against c-Met kinase activity and high selectivity versus 312 other tested protein kinases, making it one of the most selective c-Met inhibitors described to date. Moreover, this inhibitor profoundly and specifically inhibits c-Met signal transduction and thereby suppresses the c-Met-dependent neoplastic phenotype of tumor and endothelial cells.
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名称 | Glumetinib |
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Iupac 化学名称 | 6-(1-Methyl-1H-pyrazol-4-yl)-1-[[6-(1-methyl-1H-pyrazol-4-yl)imidazo[1,2-a]pyridin-3-yl]sulfonyl]-1H-pyrazolo[4,3-b]pyridine |
同义词 | Glumetinib; SCC244; SC-C244; SCC 244. |
英文同义词 | Glumetinib; SCC244; SC-C244; SCC 244. |
分子式 | C21H17N9O2S |
分子量 | 459.12 |
Smile | O=S(N1N=CC2=NC=C(C3=CN(C)N=C3)C=C21)(C4=CN=C5C=CC(C6=CN(C)N=C6)=CN54)=O |
InChiKey | RYBLECYFLJXEJX-UHFFFAOYSA-N |
InChi | InChI=1S/C21H17N9O2S/c1-27-11-16(7-24-27)14-3-4-20-23-10-21(29(20)13-14)33(31,32)30-19-5-15(6-22-18(19)9-26-30)17-8-25-28(2)12-17/h3-13H,1-2H3 |
Cas号 | 1642581-63-2 |
相关CAS号 |
包装 | 价格 | 库存 | 纯度 | 备货期 |
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大货 | 询价 | 询价 | 询价 |
外观性状 | crystalline solid |
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纯度 | 98% Min. |
存储 | 短期可在0-4度保存,数天至数月;长期可在-20度保存三年。 |
可溶性 | 可溶于DMSO;不溶于水 |
处理方式 | |
运输条件 | 可在常温下运输 |
海关编码 |
Targets | |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |
1: Ai J, Chen Y, Peng X, Ji Y, Xi Y, Shen Y, Yang X, Su Y, Sun YM, Gao Y, Ma Y,
Xiong B, Shen J, Ding J, Geng M. Preclinical evaluation of SCC244 (Glumetinib), a
novel, potent and highly selective inhibitor of c-Met in MET-dependent cancer
models. Mol Cancer Ther. 2017 Dec 13. pii: molcanther.0368.2017. doi:
10.1158/1535-7163.MCT-17-0368. [Epub ahead of print] PubMed PMID: 29237805.