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BPR1K871
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BPR1K871图片
CAS NO:2443767-35-7
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
BPR1K871是一种高效选择性的 FLT3/AURKA 双重抑制剂,对 FLT3 和 AURKA 作用的 IC50 值分别为 19 nM 和 22 nM。可作为抗癌治疗临床前开发的候选药物。
Cas No.2443767-35-7
别名DBPR114
Canonical SMILESO=C(NC1=CC(Cl)=CC=C1)NC2=NC=C(S2)CCNC3=NC=NC4=C3C=CC(OCCCN(C)C)=C4
分子式C25H28ClN7O2S
分子量526.05
溶解度DMSO: 125 mg/mL (237.62 mM)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

BPR1K871 is a potent and selective dual FLT3/AURKA inhibitor with IC50s of 19 nM and 22 nM for FLT3 and AURKA, respectively, acts as a preclinical development candidate for anti-cancer therapy[1]. IC50: 19 nM (FLT3), 22 nM (AURKA)[1]

BPR1K871 shows potent anti-proliferative activities in MOLM-13 and MV4-11 AML cells with an EC50 of ~ 5 nM[1].

BPR1K871 is a multi-kinase inhibitor for the treatment of acute myeloid leukemia (AML) and solid tumors[1].

[1]. Hsu YC, et al. Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluation. 2016 Dec 27; 7(52): 86239-86256.