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BPR1J-097 hydrochloride (1327167-19-0(free base))

🥰Excellent
Catalog No. T4261

BPR1J-097, a new-type small molecule FLT-3 inhibitor(IC50=11±7 nM), is with great anti-tumor activities in vivo.

BPR1J-097 hydrochloride (1327167-19-0(free base))

BPR1J-097 hydrochloride (1327167-19-0(free base))

🥰Excellent
Purity: 98.73%
Catalog No. T4261
BPR1J-097, a new-type small molecule FLT-3 inhibitor(IC50=11±7 nM), is with great anti-tumor activities in vivo.
Pack SizePriceAvailabilityQuantity
1 mg$43In Stock
2 mg$60In Stock
5 mg$96In Stock
10 mg$157In Stock
25 mg$285In Stock
50 mg$482In Stock
100 mg$689In Stock
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Purity:98.73%
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Product Introduction

Bioactivity
Description
BPR1J-097, a new-type small molecule FLT-3 inhibitor(IC50=11±7 nM), is with great anti-tumor activities in vivo.
Targets&IC50
MOLM-13 and MV4-11 cells:21±7 and 46±14 nM, FLT3 (D835Y):3 nM, FLT3:11±7 Nm
In vivo
In FLT3-driven AML murine xenograft models, BPR1J-097 inhibited FLT3/signal transducer and activator of transcription 5 phosphorylation and triggered apoptosis in FLT3-driven AML cells and pronounced dose-dependent tumour growth inhibition and regression.
Kinase Assay
Cells are treated with THZ531 for 6 hours.After treatment cells are washed 2-fold with cold PBS and then lysed in the following lysis buffer: Hepes(50 mM, pH 7.4), NaCl(150 mM), 1% Nonidet P40 substitute, EDTA(5 mM), DTT(1 mM), and protease/phosphatase cocktails.Lysates are treated with bio-THZ1 or bio-TH531 for pulldown overnight at 4°C.
Chemical Properties
Molecular Weight553.07
FormulaC27H29ClN6O3S
SmilesCl.CN1CCN(CC1)c1ccc(cc1)C(=O)Nc1cc([nH]n1)-c1cccc(NS(=O)(=O)c2ccccc2)c1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 5.53 mg/mL (10 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8081 mL9.0404 mL18.0809 mL90.4045 mL
5 mM0.3616 mL1.8081 mL3.6162 mL18.0809 mL
10 mM0.1808 mL0.9040 mL1.8081 mL9.0404 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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