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ABT 102

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Catalog No. T29522Cas No. 808756-71-0
Alias CHEMBL398338, ABT-102, ABT102

ABT 102 (CHEMBL398338) is a selective antagonist of transient receptor potential vanilloid 1 (TRPV1) receptor.

ABT 102

ABT 102

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Purity: 99.86%
Catalog No. T29522Alias CHEMBL398338, ABT-102, ABT102Cas No. 808756-71-0
ABT 102 (CHEMBL398338) is a selective antagonist of transient receptor potential vanilloid 1 (TRPV1) receptor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$117In StockIn Stock
5 mg$262In StockIn Stock
10 mg$388In StockIn Stock
25 mg$592In StockIn Stock
50 mg$828In StockIn Stock
100 mg$1,110In StockIn Stock
200 mg$1,480-In Stock
1 mL x 10 mM (in DMSO)$272In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Batch Information

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Purity:99.86%
ee:99.58%
Appearance:Solid
Color:White to Yellow
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Product Introduction

ABT 102 AI Summary
ABT 102 is a potent antagonist of the human TRPV1 receptor, exhibiting an IC50 of 4.0 nM for capsaicin-induced calcium flux and 0.7 nM for pH 5.5-induced activation. It also shows inhibitory activity against N-arachidonoyl-dopamine with an IC50 of 3.0 nM. The compound displays high permeability across human Caco-2 cells (Papp > 18.0 x 10^-6 cm/s) and demonstrates strong plasma protein binding (PPB 99.78%). In rats, ABT 102 has a half-life of 1.7 hours, a volume of distribution beta of 2.8 L/kg, and plasma clearance of 18.33 mL/min/kg when administered intravenously at 10 μmol/kg in PEG400. It exhibits a Cmax of 717.46 nM and an oral bioavailability of 70.0% under similar dosing conditions. Additionally, the compound decreases carrageenan-induced thermal hyperalgesia in Sprague-Dawley rats with an ED50 of 20.0 μmol/kg and shows a brain-to-plasma ratio of 0.32. The variable intrinsic clearance rates in human liver microsomes (8.32 mL/min/g) compared to rat (20.42 μL/min/(10^6 cells)) and its low intrinsic clearance in human assays suggest metabolic differences. ABT 102 demonstrates mixed effects on cell viability across different cell lines and induces hyperthermia in rats, increasing body temperature by 0.8°C. It also has varying oral bioavailability in dogs and monkeys depending on the administered dose and vehicle..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
ABT 102 (CHEMBL398338) is a selective antagonist of transient receptor potential vanilloid 1 (TRPV1) receptor.
SynonymsCHEMBL398338, ABT-102, ABT102
Chemical Properties
Molecular Weight348.44
FormulaC21H24N4O
Cas No.808756-71-0
SmilesN(C(NC1=C2C(NN=C2)=CC=C1)=O)[C@H]3C=4C(=CC(C(C)(C)C)=CC4)CC3
Relative Density.1.31g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 45 mg/mL (129.15 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2 mg/mL (5.74 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8699 mL14.3497 mL28.6993 mL143.4967 mL
5 mM0.5740 mL2.8699 mL5.7399 mL28.6993 mL
10 mM0.2870 mL1.4350 mL2.8699 mL14.3497 mL
20 mM0.1435 mL0.7175 mL1.4350 mL7.1748 mL
50 mM0.0574 mL0.2870 mL0.5740 mL2.8699 mL
100 mM0.0287 mL0.1435 mL0.2870 mL1.4350 mL

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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
μL
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

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