6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
中文名称 | 6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺 |
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中文同义词 | 6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺;化合物 T8817 |
英文名称 | 6-(4-METHOXYPHENYL)FURO[2,3-D]PYRIMIDIN-4-AMINE |
英文同义词 | 6-(4-METHOXYPHENYL)FURO[2,3-D]PYRIMIDIN-4-AMINE;6-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin-4-ylamine;Kinase IN-1;TIE-2/VEGFR-2 kinase-IN-1;Furo[2,3-d]pyrimidin-4-amine, 6-(4-methoxyphenyl)- |
CAS号 | 453590-24-4 |
分子式 | C13H11N3O2 |
分子量 | 241.25 |
EINECS号 | |
相关类别 | |
Mol文件 | 453590-24-4.mol |
结构式 |
6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺 性质
沸点 | 450.4±45.0 °C(Predicted) |
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密度 | 1.308±0.06 g/cm3(Predicted) |
储存条件 | Store at -20°C |
溶解度 | DMSO:5 mg/mL(20.73 mM;超声加热并加热至 80°C) |
形态 | 固体 |
酸度系数(pKa) | 4.73±0.40(Predicted) |
颜色 | 黄至棕色 |
Angiopoieten 1 is a ligand for the endotheiium-specific receptor tyrosine kinase, TIE-2 is a novel angiogenic factor.Inhibition of TIE-2 is expected to serve to disrupt remodeling and maturation of new vasculature initiated by angiogenesis thereby disrupting the angiogenic process. Inhibition at the kinase domain binding site of VEGFR-2 would block phosphorylation of tyrosine residues and serve to disrupt initiation of angiogenesis.
安全信息
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/04/30 | HY-112294 | TIE-2/VEGFR-2 kinase-IN-1 | 10 mM * 1 mLin DMSO | 6050元 | |
2024/01/25 | HY-112294 | TIE-2/VEGFR-2 kinase-IN-1 | 453590-24-4 | 1mg | 2500元 |