CAS NO: | 267243-28-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
1 g | 电议 |
生物活性 |
Canertinib (CI-1033;PD-183805) is a potent and irreversibleEGFRinhibitor; inhibits cellularEGFRandErbB2autophosphorylation withIC50s of 7.4 and 9 nM. Canertinib is active against vaccinia virus respiratoryinfectionin mice[1][2][3][4]. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
Canertinib significantly inhibits growth of cultured melanoma cells, RaH3 and RaH5, in a dose-dependent manner. IC50is approximately 0.8 μM and by 5μM both cell lines are completely growth-arrested within 72 h of treatment. Incubation of exponentially growing RaH3 and RaH5 with 1 μM canertinib accumulated the cells in the G1-phase of the cell cycle within 24 h of treatment without induction of apoptosis. 1 μM canertinib inhibits ErbB1-3 receptor phosphorylation with a concomitant decrease of Akt-, Erk1/2- and Stat3 activity in both cell lines[2].
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体内研究 (In Vivo) |
Canertinib shows superiorin vivoantitumor activity, giving growth delays in A431 xenografts exceeding 50 days following oral administration[1]. The growth of human malignant melanoma xenografts, RaH3 and RaH5, in nude mice is significantly inhibited by i.p. injections of 40 mg/kg/day canertinib (Fig. 4). The anti-proliferative effect on melanoma xenografts is visible already within 4 days of treatment and further increased throughout the treatment period as observed through the differences in tumor volumes, reaching statistical significance within 18 days of treatment[2].
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Clinical Trial |
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分子量 |
485.94 |
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性状 |
Solid |
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Formula |
C24H25ClFN5O3 |
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CAS 号 |
267243-28-7 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
Ethanol : 12.5 mg/mL(25.72 mM;Need ultrasonic) DMSO : 4.9 mg/mL(10.08 mM;Need warming)
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In Vivo:
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