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VAP-1-IN-2

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Catalog No. T218652 Copy Product Info
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VAP-1-IN-2 is an orally active VAP-1 inhibitor, with an IC50 value of 0.025 μM for humans and 0.015 μM for rats. It reduces urinary protein excretion and the progression of proteinuria in diabetic rats. VAP-1-IN-2 inhibits VAP-1 activity in rats and is applicable in research related to diabetes and kidney disease.

VAP-1-IN-2

Cas No. 1279026-89-9
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
VAP-1-IN-2 is an orally active VAP-1 inhibitor, with an IC50 value of 0.025 μM for humans and 0.015 μM for rats. It reduces urinary protein excretion and the progression of proteinuria in diabetic rats. VAP-1-IN-2 inhibits VAP-1 activity in rats and is applicable in research related to diabetes and kidney disease.
In vitro
VAP-1-IN-2 (Compound 1/17hd) is a potent inhibitor of recombinant human VAP-1, with an IC50 of 0.025 μM, and also effectively inhibits recombinant rat VAP-1, with an IC50 of 0.015 μM.
In vivo
VAP-1-IN-2, administered orally at doses of 0.3-1 mg/kg as a single treatment, is capable of inhibiting VAP-1 activity in rats. Additionally, VAP-1-IN-2, given orally at 0.3-1 mg/kg once daily for 4 weeks, significantly reduces the progression of proteinuria and plasma VAP-1 activity in rats with Streptozotocin-induced diabetes.
Chemical Properties
Molecular Weight494.97
FormulaC25H27ClN6O3
Cas No.1279026-89-9
SmilesO=C(O)C1=CC=C(C(Cl)=C1)N2CCN(C=3N=CC(=CN3)C4=CC=CC(=C4)CN(C(=O)CN)C)CC2
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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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 µL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 µL Tween 80 and mix well until fully clarified.

3) Add 450 µL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: VAP-1-IN-2 in vivo | VAP-1-IN-2 in vitro | VAP-1-IN-2 formula | VAP-1-IN-2 molecular weight