溶解性 | Soluble in DMSO (2 mg/ml), methanol, ethanol (9 mg/ml), and water (<1 mg/ml). |
存贮条件 | 储存温度-20°C |
应用 | An irreversible pan-erbB tyrosine kinase inhibitor. |
产品介绍 | Canertinib (CI-1033)是一种pan-ErbB抑制剂,同时抑制EGFR和ErbB2,IC50分别为1.5 nM和9.0 nM,但对PDGFR, FGFR, InsR, PKC,和CDK1/2/4等均无抑制活性。 |
备注 | Canertinib (CI-1033) is a pan-ErbB inhibitor for EGFR and ErbB2 with IC50 of 1.5 nM and 9.0 nM, no activity to PDGFR, FGFR, InsR, PKC, or CDK1/2/4. Phase 3. |
生化机理 | Canertinib is a potent and selective inhibitor of tyrosine residue phosphorylation of EGFR, blocking signal transgression and ceasing angiogenisis. Canertinib displays an IC50 = 1.5nM. Additionally, Canertinib’s action in inhibiting EGFR increases apoptosis in cancerous cell lines in a titratable fashion. |
别名 | PD-183805;卡奈替尼; 卡耐替尼;N-[4-[(3-氯-4-氟苯基)氨基]-7-(3-吗啉-4-基丙氧基)喹唑啉-6-基]丙-2-烯酰胺;卡那替尼;;CI-1033;CI1033;CI 1033;PD183805;PD 183805;N-[4-(3-Chloro-4-fluoroanilino)-7-(3-morpholinopropoxy)quinazolin-6-yl]acrylamide |