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Canertinib dihydrochloride

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产品价格:电议      采购度:1610      原产地:美洲

发布时间:2021/7/23 23:48:27      所属地区:上海 上海市

简要描述:

Canertinib dihydrochloride (CI-1033;PD-183805) 是有效地,不可逆的 EGFR 抑制剂;抑制细胞 EGFR 和 ErbB2 自身磷酸化的 IC50 值分别为 9 nM。

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标签:CI-1033   dihydrochloride   

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Canertinib dihydrochloride

CAS No. : 289499-45-2

MCE 站:Canertinib dihydrochloride

产品活性:Canertinib dihydrochloride (CI-1033;PD-183805) 是有效地,不可逆的 EGFR 抑制剂;抑制细胞 EGFRErbB2 自身磷酸化的 IC50 值分别为 7.4和 9 nM。

研究领域:JAK/STAT Signaling  |  Protein Tyrosine Kinase/RTK

作用靶点:EGFR

In Vitro: Canertinib dihydrochloride (CI-1033 dihydrochloride) significantly inhibits growth of cultured melanoma cells, RaH3 and RaH5, in a dose-dependent manner. IC50 is 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.
Canertinib dihydrochloride also is a potent activator of exosome secretion.

In Vivo: Canertinib dihydrochloride (CI-1033 dihydrochloride) shows superior in vivo antitumor activity, giving growth delays in A431 xenografts exceeding 50 days following oral administration. 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.

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更新时间:2024/1/2 10:14:29

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