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BI-4924

Catalog No. T14564Cas No. 2244452-09-1
Alias BI4924, BI 4924

BI-4924 is a selective and potent inhibitor of phosphoglycerate dehydrogenase (PHGDH) (IC50=3 nM) that disrupts serine biosynthesis by intracellular trapping, and can be used in the study of diseases caused by dysfunction.

BI-4924

BI-4924

Purity: 99.55%
Catalog No. T14564Alias BI4924, BI 4924Cas No. 2244452-09-1
BI-4924 is a selective and potent inhibitor of phosphoglycerate dehydrogenase (PHGDH) (IC50=3 nM) that disrupts serine biosynthesis by intracellular trapping, and can be used in the study of diseases caused by dysfunction.
Pack SizePriceAvailabilityQuantity
25 mg$1,6706-8 weeks
50 mg$2,1806-8 weeks
100 mg$2,8006-8 weeks
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Purity:99.55%
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Product Introduction

Bioactivity
Description
BI-4924 is a selective and potent inhibitor of phosphoglycerate dehydrogenase (PHGDH) (IC50=3 nM) that disrupts serine biosynthesis by intracellular trapping, and can be used in the study of diseases caused by dysfunction.
Targets&IC50
PHGDH:3 nM
In vitro
BI-4924 is a potent NADH/NAD+-competitive PHGDH inhibitor, demonstrating high selectivity against most other dehydrogenase targets[1].
AliasBI4924, BI 4924
Chemical Properties
Molecular Weight499.36
FormulaC21H20Cl2N2O6S
Cas No.2244452-09-1
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 100 mg/mL (200.26 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0026 mL10.0128 mL20.0256 mL100.1282 mL
5 mM0.4005 mL2.0026 mL4.0051 mL20.0256 mL
10 mM0.2003 mL1.0013 mL2.0026 mL10.0128 mL
20 mM0.1001 mL0.5006 mL1.0013 mL5.0064 mL
50 mM0.0401 mL0.2003 mL0.4005 mL2.0026 mL
100 mM0.0200 mL0.1001 mL0.2003 mL1.0013 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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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