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WAY-230563

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Catalog No. T202246Cas No. 93326-70-6
Alias WAY230563, WAY 230563, Oprea1_852430, Oprea1_826310, CBMicro_008038, Benzimidazole, 1-(1-naphthylsulfonyl)-

WAY-230563 is a serine/threonine kinase inhibitor.

WAY-230563

WAY-230563

😃Good
Catalog No. T202246Alias WAY230563, WAY 230563, Oprea1_852430, Oprea1_826310, CBMicro_008038, Benzimidazole, 1-(1-naphthylsulfonyl)-Cas No. 93326-70-6
WAY-230563 is a serine/threonine kinase inhibitor.
Pack SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
WAY-230563 is a serine/threonine kinase inhibitor.
AliasWAY230563, WAY 230563, Oprea1_852430, Oprea1_826310, CBMicro_008038, Benzimidazole, 1-(1-naphthylsulfonyl)-
Chemical Properties
Molecular Weight308.35
FormulaC17H12N2O2S
Cas No.93326-70-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice./Shipping at ambient temperature.

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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.
1 Enter information below:
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2 Enter the in vivo formulation:
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