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Candoxatril

(Synonyms: UK 79300) Copy Product Info
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Synonyms: UK 79300

Catalog No. T10671 Copy Product Info
Purity: 99.94%
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Candoxatril (UK 79300) is a small-molecule inhibitor and a neutral endopeptidase (NEP) inhibitor with oral activity and cell permeability, used for the treatment of chronic heart failure and capable of improving exercise capacity in patients receiving angiotensin-converting enzyme inhibitor therapy.
Candoxatril
Cas No. 123122-55-4
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$293In StockIn Stock
5 mg$719In StockIn Stock
10 mg$987-In Stock
25 mg$1,490-In Stock
50 mg$1,980-In Stock
100 mg$2,750-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.94%
ee:99.84%
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Product Introduction

Bioactivity
Description
Candoxatril (UK 79300) is a small-molecule inhibitor and a neutral endopeptidase (NEP) inhibitor with oral activity and cell permeability, used for the treatment of chronic heart failure and capable of improving exercise capacity in patients receiving angiotensin-converting enzyme inhibitor therapy.
In vivo
Methods: A unilateral ureteral obstruction (UUO)-induced renal fibrosis mouse model was used. Candoxatril was administered orally daily at an unspecified dose for 1 consecutive week.
Results: Compared with the vehicle control group, Candoxatril significantly increased urinary cGMP levels, reduced renal cortical collagen deposition (from 1.8% to 0.8%) and α-SMA expression (from 8.3% to 4.9%), demonstrating anti-fibrotic effects. [1]
Methods: An anesthetized mouse model was used. Candoxatril (5 mg/kg, dissolved in 0.9% NaCl) was administered by intravenous injection, followed by GLP-1(9-36)NH₂ injection 2 minutes later.
Results: Compared with the vehicle control group, the Candoxatril pretreatment group showed significantly elevated immunoreactive GLP-1 concentration, indicating effective inhibition of NEP 24.11-mediated degradation of GLP-1 metabolites. [2]
SynonymsUK 79300
Chemical Properties
Molecular Weight515.64
FormulaC29H41NO7
Cas No.123122-55-4
SmilesC([C@H](C(OC=1C=C2C(=CC1)CCC2)=O)COCCOC)C3(C(N[C@H]4CC[C@@H](C(O)=O)CC4)=O)CCCC3
Relative Density.1.21g/cm3
Storage & Solubility Information
StorageStore at low temperature Pure form: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 50 mg/mL (96.97 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Saline: 5 mg/mL (9.7 mM), Suspension.
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 mM1.9393 mL9.6967 mL19.3934 mL96.9669 mL
5 mM0.3879 mL1.9393 mL3.8787 mL19.3934 mL
10 mM0.1939 mL0.9697 mL1.9393 mL9.6967 mL
20 mM0.0970 mL0.4848 mL0.9697 mL4.8483 mL
50 mM0.0388 mL0.1939 mL0.3879 mL1.9393 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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

Keywords

Related Tags: Candoxatril chemical structure | Candoxatril in vivo | Candoxatril formula | Candoxatril molecular weight