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Amb21795397

Amb21795397
Amb21795397 is a blocker of the MARV VP40 PPxY-host Nedd4 interaction.
Catalog No. T23715Cas No. 1797967-45-3

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Amb21795397

Catalog No. T23715Alias PPxY Budding Inhibitor 5, Amb-21795397, Amb 21795397Cas No. 1797967-45-3

Amb21795397 is a blocker of the MARV VP40 PPxY-host Nedd4 interaction.
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.
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
Amb21795397 is a blocker of the MARV VP40 PPxY-host Nedd4 interaction.
AliasPPxY Budding Inhibitor 5, Amb-21795397, Amb 21795397
Chemical Properties
Molecular Weight352.41
FormulaC18H16N4O2S
Cas No.1797967-45-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping 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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