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Y08175

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Catalog No. T62713Cas No. 2223014-57-9

Y08175 is a potent inhibitor of CBP Bromodomain. y08175 has an IC50 of 37 and 178.15 nM against CBP in the AlphaScreen and HTRF assays, respectively. y08175 can be used to study prostate cancer.

Y08175

Y08175

😃Good
Catalog No. T62713Cas No. 2223014-57-9
Y08175 is a potent inhibitor of CBP Bromodomain. y08175 has an IC50 of 37 and 178.15 nM against CBP in the AlphaScreen and HTRF assays, respectively. y08175 can be used to study prostate cancer.
Pack SizePriceAvailabilityQuantity
25 mg$1,5206-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
Y08175 is a potent inhibitor of CBP Bromodomain. y08175 has an IC50 of 37 and 178.15 nM against CBP in the AlphaScreen and HTRF assays, respectively. y08175 can be used to study prostate cancer.
Chemical Properties
Molecular Weight450.42
FormulaC23H19FN4O5
Cas No.2223014-57-9
Storage & Solubility Information
StorageShipping with blue ice.

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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% 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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