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Captopril

🥰Excellent
Catalog No. T1462Cas No. 62571-86-2
Alias SQ-14534, SQ 14225, SA333

Captopril (SA333) is a potent and specific inhibitor of peptidyl-dipeptidase A. It blocks the conversion of angiotensin I to angiotensin II, a vasoconstrictor and important regulator of arterial blood pressure.

Captopril

Captopril

🥰Excellent
Purity: 99.88%
Catalog No. T1462Alias SQ-14534, SQ 14225, SA333Cas No. 62571-86-2
Captopril (SA333) is a potent and specific inhibitor of peptidyl-dipeptidase A. It blocks the conversion of angiotensin I to angiotensin II, a vasoconstrictor and important regulator of arterial blood pressure.
Pack SizePriceAvailabilityQuantity
50 mg$40In Stock
100 mg$48In Stock
200 mg$59In Stock
500 mg$81In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Purity:99.88%
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Product Introduction

Bioactivity
Description
Captopril (SA333) is a potent and specific inhibitor of peptidyl-dipeptidase A. It blocks the conversion of angiotensin I to angiotensin II, a vasoconstrictor and important regulator of arterial blood pressure.
Targets&IC50
ACE:6 nM
Kinase Assay
Binding assay: Cells are plated in 24-well plates and cultured until confluence. Before the experiment, the cells are washed three times with 0.5 mL per well of DMEM at room temperature. After removal of the medium, 400 μL binding DMEM is added and the plate is then left for 15 min at 37 ℃. For saturation binding assays cells are incubated with increasing concentrations [3H]Candesartan (final concentrations between 0.15 nM and 15 nM) in a final volume of 0.5 mL at 37 ℃ for 5 min to 180 min. For competition binding assays 50 μL of buffer or 50 μL of buffer containing increasing concentrations of unlabelled Candesartan is added. After 30 min, 50 μL of buffer containing [3H]Candesartan (final concentration 1.1 nM) or [3H]Candesartan (final concentration 1.0 nM) is added, and the cells are further incubated for 30 min at 37 ℃.
AliasSQ-14534, SQ 14225, SA333
Chemical Properties
Molecular Weight217.29
FormulaC9H15NO3S
Cas No.62571-86-2
SmilesC[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O
Relative Density.1.2447 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 21.7 mg/mL (100 mM)
DMSO: 50 mg/mL (230.11 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM4.6021 mL23.0107 mL46.0214 mL230.1072 mL
5 mM0.9204 mL4.6021 mL9.2043 mL46.0214 mL
10 mM0.4602 mL2.3011 mL4.6021 mL23.0107 mL
20 mM0.2301 mL1.1505 mL2.3011 mL11.5054 mL
50 mM0.0920 mL0.4602 mL0.9204 mL4.6021 mL
100 mM0.0460 mL0.2301 mL0.4602 mL2.3011 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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