SAR125844
产品编号: DC7672
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应用领域
SAR125844 是一种有效的、高度选择性的、可逆的、ATP竞争性的 MET受体酪氨酸激酶 (RTK) 的抑制剂,其IC50 值为4.2 nM。能抑制细胞中MET的自磷酸化。
Cas No.: |
1116743-46-4 |
名称: |
1-(6-((6-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)thio)benzo[d]thiazol-2-yl)-3-(2-morpholinoethyl)urea |
别名: |
SAR125844; SAR 125844; SAR-125844 |
SMILES: |
O=C(NCCN1CCOCC1)NC2=NC3=CC=C(SC4=NN=C5C=CC(C6=CC=C(F)C=C6)=NN54)C=C3S2 |
分子式: |
C25H23FN8O2S2 |
分子量: |
550.63 |
纯度: |
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保存条件: |
2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: |
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In Vivo: |
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In Vitro: |
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References: |
SAR125844 is inhibitor of the proto-oncogene c-Met (also known as hepatocyte growth factor receptor [HGFR]) with potential antineoplastic activity. Upon intravenous administration, c-Met inhibitor SAR125844 binds to c-Met, thereby disrupting c-Met-mediat |
Kinase Assay: |
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Cell Assay: |
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Animal Administration: |
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References: |
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MSDS
COA
LOT NO. |
DOWNLOAD |
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2018-0101 |
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