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ADX68692

(Synonyms: ADX 68692) Copy Product Info
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Synonyms: ADX 68692

Catalog No. T217657 Copy Product Info
Purity: 99.59%
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ADX68692 is an orally active negative allosteric modulator that targets the follicle-stimulating hormone receptor (FSHR). ADX68692 exerts its regulatory effect primarily by inhibiting FSHR-mediated cAMP production and can be used in research into reproductive system disorders associated with abnormal FSH/FSHR signalling.
ADX68692
Cas No. 1067191-08-5
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Pack SizePriceEUR StockGlobal StockQuantity
1 mg175 €-In Stock
5 mg434 €-In Stock
10 mg621 €-In Stock
25 mg972 €-In Stock
50 mg1.341 €-In Stock
For In stock only · Estimated delivery: EUR 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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Purity:99.59%
Appearance:Solid
Color:Yellow
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Product Information

Bioactivity
Description
ADX68692 is an orally active negative allosteric modulator that targets the follicle-stimulating hormone receptor (FSHR). ADX68692 exerts its regulatory effect primarily by inhibiting FSHR-mediated cAMP production and can be used in research into reproductive system disorders associated with abnormal FSH/FSHR signalling.
In vivo
Method: Mature female rats received ADX68692 by oral gavage at 10 or 25 mg/kg. Estrous cycling and FSH-induced progesterone, estradiol, oocyte release and preovulatory follicle formation were evaluated.Result:
Both doses disrupted estrous cycling. At 25 mg/kg, ADX68692 reduced FSH-induced progesterone and estradiol production, oocyte release and formation of preovulatory follicles.[1]
SynonymsADX 68692
Chemical Properties
Molecular Weight401.4577
FormulaC24H23N3O3
Cas No.1067191-08-5
SmilesCOC1=C(OC)C=C(C=C1)C(=O)NC1=CC(C2=CN=CC=C2)=C(C=C1)C(C)(C)C#N
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 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:
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2 Enter the in vivo formulation:
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Related Tags: ADX68692 chemical structure | ADX68692 in vivo | ADX68692 formula | ADX68692 molecular weight