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BMS-214662

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Catalog No. T10567Cas No. 195987-41-8

BMS-214662 is a potent and selective farnesyl transferase inhibitor that induces mitochondrial apoptosis in primitive CD34+ chronic myeloid leukemia (CML) stem cells/progenitors and selectively targets CML stem cells/progenitors with antitumor activity.

BMS-214662

BMS-214662

😃Good
Catalog No. T10567Cas No. 195987-41-8
BMS-214662 is a potent and selective farnesyl transferase inhibitor that induces mitochondrial apoptosis in primitive CD34+ chronic myeloid leukemia (CML) stem cells/progenitors and selectively targets CML stem cells/progenitors with antitumor activity.
Pack SizePriceAvailabilityQuantity
25 mg$2,27010-14 weeks
50 mg$2,98010-14 weeks
100 mg$4,00010-14 weeks
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Product Introduction

Bioactivity
Description
BMS-214662 is a potent and selective farnesyl transferase inhibitor that induces mitochondrial apoptosis in primitive CD34+ chronic myeloid leukemia (CML) stem cells/progenitors and selectively targets CML stem cells/progenitors with antitumor activity.
Targets&IC50
KRas:2.3 μM , Ras-CVLL:1.3 μM , FTase:1.35 nM
Chemical Properties
Molecular Weight489.61
FormulaC25H23N5O2S2
Cas No.195987-41-8
Relative Density.1.45 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: 100 mg/mL (204.24 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0424 mL10.2122 mL20.4244 mL102.1221 mL
5 mM0.4085 mL2.0424 mL4.0849 mL20.4244 mL
10 mM0.2042 mL1.0212 mL2.0424 mL10.2122 mL
20 mM0.1021 mL0.5106 mL1.0212 mL5.1061 mL
50 mM0.0408 mL0.2042 mL0.4085 mL2.0424 mL
100 mM0.0204 mL0.1021 mL0.2042 mL1.0212 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
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
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