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BPR1K871

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Catalog No. T10592Cas No. 2443767-35-7
Alias DBPR114

BPR1K871, a preclinical development candidate for anti-cancer therapy [1], is a potent, selective dual inhibitor targeting FLT3 and AURKA, with IC50 values of 19 nM and 22 nM, respectively.

BPR1K871

BPR1K871

😃Good
Catalog No. T10592Alias DBPR114Cas No. 2443767-35-7
BPR1K871, a preclinical development candidate for anti-cancer therapy [1], is a potent, selective dual inhibitor targeting FLT3 and AURKA, with IC50 values of 19 nM and 22 nM, respectively.
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10 mg$1,2407-10 days
25 mg$2,1307-10 days
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Product Introduction

Bioactivity
Description
BPR1K871, a preclinical development candidate for anti-cancer therapy [1], is a potent, selective dual inhibitor targeting FLT3 and AURKA, with IC50 values of 19 nM and 22 nM, respectively.
Targets&IC50
AURKA:22 nM , FLT3:19 nM
In vitro
BPR1K871 demonstrates strong anti-proliferative effects on MOLM-13 and MV4-11 AML cells, achieving an EC50 of approximately 5 nM [1].
In vivo
BPR1K871, a multi-kinase inhibitor, is utilized for the treatment of acute myeloid leukemia (AML) and solid tumors [1].
AliasDBPR114
Chemical Properties
Molecular Weight526.05
FormulaC25H28ClN7O2S
Cas No.2443767-35-7
Relative Density.1.387 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 125 mg/mL (237.62 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9010 mL9.5048 mL19.0096 mL95.0480 mL
5 mM0.3802 mL1.9010 mL3.8019 mL19.0096 mL
10 mM0.1901 mL0.9505 mL1.9010 mL9.5048 mL
20 mM0.0950 mL0.4752 mL0.9505 mL4.7524 mL
50 mM0.0380 mL0.1901 mL0.3802 mL1.9010 mL
100 mM0.0190 mL0.0950 mL0.1901 mL0.9505 mL

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