6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
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- CAS号:
- 453590-24-4
- 英文名:
- 6-(4-METHOXYPHENYL)FURO[2,3-D]PYRIMIDIN-4-AMINE
- 英文别名:
- Kinase IN-1;TIE-2/VEGFR-2 kinase-IN-1;6-(4-METHOXYPHENYL)FURO[2,3-D]PYRIMIDIN-4-AMINE;Furo[2,3-d]pyrimidin-4-amine, 6-(4-methoxyphenyl)-;6-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin-4-ylamine
- 中文名:
- 6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
- 中文别名:
- 化合物 T8817;6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
- CBNumber:
- CB92446346
- 分子式:
- C13H11N3O2
- 分子量:
- 241.25
- MOL File:
- 453590-24-4.mol
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6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺化学性质
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沸点:
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450.4±45.0 °C(Predicted)
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密度:
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1.308±0.06 g/cm3(Predicted)
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储存条件:
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Store at -20°C
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溶解度:
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DMSO: 5 mg/mL (20.73 mM; ultrasonic and warming and heat to 80°C)
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酸度系数(pKa):
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4.73±0.40(Predicted)
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6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺性质、用途与生产工艺
TIE-2/VEGFR-2 kinase-IN-1 用于合成 TIE-2 或者 VEGFR-2 抑制剂，从专利 WO2003022852 中获得，例 14。TIE-2/VEGFR-2 kinase-IN-1 用于研究不适当的血管生成相关疾病。
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.
6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
上下游产品信息
上游原料
下游产品
| 更新日期 | 产品编号 | 产品名称 | CAS编号 | 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 |
6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
生产厂家
453590-24-4, 6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺 相关搜索:
- 化合物 T8817
- 6-(4-甲氧基苯基)呋喃并[2,3-D]嘧啶-4-胺
- 453590-24-4
- Furo[2,3-d]pyrimidin-4-amine, 6-(4-methoxyphenyl)-
- TIE-2/VEGFR-2 kinase-IN-1
- Kinase IN-1
- 6-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin-4-ylamine
- 6-(4-METHOXYPHENYL)FURO[2,3-D]PYRIMIDIN-4-AMINE