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BAY-252

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Catalog No. T78148Cas No. 2639638-67-6
Alias BAY252

BAY-252 is a potent inhibitor of branched-chain amino acid transaminases 1 (BCAT1) and BCAT2, with IC50 of 2 μM for both enzymes. In addition to its inhibitory properties, BAY-252 serves as a chemical probe in cancer research, aiding in the investigation of metabolic pathways involving branched-chain amino acids.

BAY-252

BAY-252

😃Good
Catalog No. T78148Alias BAY252Cas No. 2639638-67-6
BAY-252 is a potent inhibitor of branched-chain amino acid transaminases 1 (BCAT1) and BCAT2, with IC50 of 2 μM for both enzymes. In addition to its inhibitory properties, BAY-252 serves as a chemical probe in cancer research, aiding in the investigation of metabolic pathways involving branched-chain amino acids.
Pack SizePriceAvailabilityQuantity
5 mgInquiry8-10 weeks
50 mgInquiry8-10 weeks
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
Description
BAY-252 is a potent inhibitor of branched-chain amino acid transaminases 1 (BCAT1) and BCAT2, with IC50 of 2 μM for both enzymes. In addition to its inhibitory properties, BAY-252 serves as a chemical probe in cancer research, aiding in the investigation of metabolic pathways involving branched-chain amino acids.
In vitro
BAY-252 inhibits the proliferation of MDA-MB-231 cells with an IC50 value of 2 μM [1].
SynonymsBAY252
Chemical Properties
Molecular Weight446.81
FormulaC22H14ClF3N2O3
Cas No.2639638-67-6
SmilesO=C1C=C(NC(=O)N1C2=CC(OC=3C=CC=CC3C)=C(Cl)C=4C=CC=CC42)C(F)(F)F
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 100 mg/mL (223.81 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2381 mL11.1904 mL22.3809 mL111.9044 mL
5 mM0.4476 mL2.2381 mL4.4762 mL22.3809 mL
10 mM0.2238 mL1.1190 mL2.2381 mL11.1904 mL
20 mM0.1119 mL0.5595 mL1.1190 mL5.5952 mL
50 mM0.0448 mL0.2238 mL0.4476 mL2.2381 mL
100 mM0.0224 mL0.1119 mL0.2238 mL1.1190 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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% Saline/PBS/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 μLSaline/PBS/ddH2OTargetMol | 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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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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