EGF/FGF/PDGF受体酪氨酸激酶抑制剂结构式
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常用名 | EGF/FGF/PDGF受体酪氨酸激酶抑制剂 | 英文名 | EGF/FGF/PDGF receptor tyrosine kinase inhibitor |
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CAS号 | 1135256-66-4 | 分子量 | 405.28 | |
密度 | ~1.4 g/cm3(Predicted) | 沸点 | 594.56° C (Predicted) | |
分子式 | C18H18Cl2N6O | 熔点 | 256.77° C (Predicted) | |
MSDS | N/A | 闪点 | N/A |
EGF/FGF/PDGF受体酪氨酸激酶抑制剂用途EGF / FGF / PDGF受体酪氨酸激酶抑制剂是一种细胞可渗透且可逆的蛋白酪氨酸激酶抑制剂,可抑制人Flg(FGFR-1),PDGFR-β,c-Scr和EGFR,同时对InsR,PKC,或CDK4 / Cyclin D1。EGF / FGF / PDGF受体酪氨酸激酶抑制剂的抑制作用在c-Src情况下显示为非竞争性,在Flg(FGFR-1),PDGFR-β和EGFR情况下显示为ATP竞争性。 EGF/FGF/PDGF Receptor Tyrosine Kinase Inhibitor is a cell-permeable and reversible protein tyrosine kinase inhibitor that inhibits human Flg (FGFR-1), PDGFR-β, c-Scr, and EGFR, meanwhile exhibiting minimal activity against InsR, PKC, or CDK4/Cyclin D1. Inhibition by EGF/FGF/PDGF Receptor Tyrosine Kinase Inhibitor is shown to be noncompetitive in the case of c-Src, but ATP-competitive in the case of Flg (FGFR-1), PDGFR-β, and EGFR. |
中文名 | EGF/FGF/PDGF受体酪氨酸激酶抑制剂 |
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英文名 | EGF/FGF/PDGF receptor tyrosine kinase inhibitor |
英文别名 | 更多 |
密度 | ~1.4 g/cm3(Predicted) |
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沸点 | 594.56° C (Predicted) |
熔点 | 256.77° C (Predicted) |
分子式 | C18H18Cl2N6O |
分子量 | 405.28 |
精确质量 | 404.091919 |
LogP | 2.12 |
折射率 | n20D1.69 (Predicted) |
储存条件 | 2-8°C储存 |
水溶解性 | Soluble in DMSO (25 mg/ml), and ethanol (1 mg/ml). |
1-(2-Amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-yl)-3-tert-butyl urea |
PDGFR Tyrosine Kinase Inhibitor XIII |
PD 089828 |
Urea, N-[2-amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-yl]-N'-(1,1-dimethylethyl)- |
1-[2-amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea |
1-[2-Amino-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-7-yl]-3-(2-methyl-2-propanyl)urea |