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Zofenopril calcium

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Catalog No. T5030Cas No. 81938-43-4
Alias Zofenopril (calcium), SQ26991

Zofenopril calcium (SQ26991) is an antioxidant that acts as an angiotensin-converting enzyme inhibitor. ACE Zofenopril is a pro-drug designed to undergo metabolic hydrolysis yielding the active free sulfhydryl compound zofenoprilat, which is an angiotensin converting enzyme (ACE) inhibitor . Zofenopril promotes the regeneration of peripheral nerve injuries in rat models . Zofenopril increases SR calcium cycling and stimulates active calcium uptake into the SR .

Zofenopril calcium

Zofenopril calcium

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Purity: 98.37%
Catalog No. T5030Alias Zofenopril (calcium), SQ26991Cas No. 81938-43-4
Zofenopril calcium (SQ26991) is an antioxidant that acts as an angiotensin-converting enzyme inhibitor. ACE Zofenopril is a pro-drug designed to undergo metabolic hydrolysis yielding the active free sulfhydryl compound zofenoprilat, which is an angiotensin converting enzyme (ACE) inhibitor . Zofenopril promotes the regeneration of peripheral nerve injuries in rat models . Zofenopril increases SR calcium cycling and stimulates active calcium uptake into the SR .
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$34In StockIn Stock
10 mg$59In StockIn Stock
25 mg$131In StockIn Stock
50 mg$243In StockIn Stock
100 mg$353In StockIn Stock
200 mg$495InquiryInquiry
1 mL x 10 mM (in DMSO)$59In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.37%
Appearance:Solid
Color:White
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Product Introduction

Zofenopril calcium AI Summary
Zofenopril calcium exhibits antiviral activity against SARS-CoV-2 by multiple mechanisms. It inhibits the viral-induced cytotoxicity in Caco-2 and VERO-6 cells at a concentration of 10 µM after 48 hours, showing inhibition rates of -2.97% and -0.09%, respectively, as determined by high content imaging. Additionally, it shows moderate effectiveness against the SARS-CoV-2 (USA-WA1/2020 strain) in HRCE cells at a MOI of 0.4 after 96 hours, with a hit score of 0.2305. Moreover, the compound inhibits the SARS-CoV-2 3CL-Pro protease by approximately 2.577% at a concentration of 20 µM, based on a FRET response from a peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Zofenopril calcium (SQ26991) is an antioxidant that acts as an angiotensin-converting enzyme inhibitor. ACE Zofenopril is a pro-drug designed to undergo metabolic hydrolysis yielding the active free sulfhydryl compound zofenoprilat, which is an angiotensin converting enzyme (ACE) inhibitor . Zofenopril promotes the regeneration of peripheral nerve injuries in rat models . Zofenopril increases SR calcium cycling and stimulates active calcium uptake into the SR .
SynonymsZofenopril (calcium), SQ26991
Chemical Properties
Molecular Weight897.17
FormulaC44H44CaN2O8S4
Cas No.81938-43-4
Smiles[Ca++].C[C@H](CSC(=O)c1ccccc1)C(=O)N1C[C@H](C[C@H]1C([O-])=O)Sc1ccccc1.C[C@H](CSC(=O)c1ccccc1)C(=O)N1C[C@H](C[C@H]1C([O-])=O)Sc1ccccc1
Relative Density.1.34 g/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: 8.98 mg/mL (10.01 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.1146 mL5.5731 mL11.1462 mL55.7308 mL
5 mM0.2229 mL1.1146 mL2.2292 mL11.1462 mL
10 mM0.1115 mL0.5573 mL1.1146 mL5.5731 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:
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2 Enter the in vivo formulation:
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