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HSD17B13-IN-20

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Catalog No. T86627Cas No. 2919797-59-2

HSD17B13-IN-38 (Compound 18.02), an inhibitor of hydroxysteroid 17β-dehydrogenase 13 (HSD17B13), is utilized in the study of various liver diseases including hepatitis, liver fibrosis, liver cirrhosis, and hepatocellular carcinoma [1].

HSD17B13-IN-20

HSD17B13-IN-20

😃Good
Catalog No. T86627Cas No. 2919797-59-2
HSD17B13-IN-38 (Compound 18.02), an inhibitor of hydroxysteroid 17β-dehydrogenase 13 (HSD17B13), is utilized in the study of various liver diseases including hepatitis, liver fibrosis, liver cirrhosis, and hepatocellular carcinoma [1].
Pack SizePriceAvailabilityQuantity
10 mgInquiry10-14 weeks
50 mgInquiry10-14 weeks
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Product Introduction

Bioactivity
Description
HSD17B13-IN-38 (Compound 18.02), an inhibitor of hydroxysteroid 17β-dehydrogenase 13 (HSD17B13), is utilized in the study of various liver diseases including hepatitis, liver fibrosis, liver cirrhosis, and hepatocellular carcinoma [1].
Chemical Properties
Molecular Weight534.5
FormulaC21H23F5N6O3S
Cas No.2919797-59-2
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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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