BCR-ABL-IN-3

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

BCR-ABL-IN-3 

BCR-ABL-IN-3 是一种有效且不可逆的 Bcr-Abl 抑制剂,对于 Ba/F3Bcr-AblT3151IC50 为 ≤100 nM。BCR-ABL-IN-3 具有抗癌活性。

BCR-ABL-IN-3

BCR-ABL-IN-3 Chemical Structure

CAS No. : 2240191-12-0

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生物活性

BCR-ABL-IN-3 is a potent and irreversible Bcr-Abl inhibitor with an IC50 of ≤100 nM for Ba/F3Bcr-AblT3151. BCR-ABL-IN-3 has anti-cancer activity[1].

IC50 & Target[1]

Ba/F3Bcr-AblT3151

≤100 nM (IC50)

体内研究
(In Vivo)

BCR-ABL-IN-3 (compound 7; 15 mg/kg; twice a day; for 19 days) has good antitumor effect in female NOD/SCID mice of 7-8 weeks weighing 21.8 g with Ba/F3Bcr-AblT3151 cells[1].
BCR-ABL-IN-3 (2 mg/kg for IV or 20mg/kg for PO) has a Cmax of 5485 ng/mL and an AUC of 5450 h•ng/mL for IV in male Sprague Dawley rats of 7-8 weeks old weighing 210 g[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

466.89

Formula

C20H17ClF2N4O3S

CAS 号

2240191-12-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Hanyi Wang, et al. (hetero)arylamide compound for inhibiting protein kinase activity. WO2018133826A1.

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