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Brinazarone

Catalog No. T88246Cas No. 89622-90-2
Alias SR 33287

Brinazarone (SR 33287) serves as an inhibitor of acid lysosomal sphingomyelinase, subsequently causing cellular lipidosis. It enhances the cytotoxic effects of anti-Thy 1.2 AT15E RTA-IT on T2 cells and anti-CD5 T101 on CEM cells.

Brinazarone

Brinazarone

Catalog No. T88246Alias SR 33287Cas No. 89622-90-2
Brinazarone (SR 33287) serves as an inhibitor of acid lysosomal sphingomyelinase, subsequently causing cellular lipidosis. It enhances the cytotoxic effects of anti-Thy 1.2 AT15E RTA-IT on T2 cells and anti-CD5 T101 on CEM cells.
Pack SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
Brinazarone (SR 33287) serves as an inhibitor of acid lysosomal sphingomyelinase, subsequently causing cellular lipidosis. It enhances the cytotoxic effects of anti-Thy 1.2 AT15E RTA-IT on T2 cells and anti-CD5 T101 on CEM cells.
AliasSR 33287
Chemical Properties
Molecular Weight392.53
FormulaC25H32N2O2
Cas No.89622-90-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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