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Cronidipine

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Catalog No. T27087Cas No. 113759-50-5
Alias LF-20254, LF20254, LF 20254, LF 2.0254

Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.

Cronidipine

Cronidipine

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Purity: 99.47%
Catalog No. T27087Alias LF-20254, LF20254, LF 20254, LF 2.0254Cas No. 113759-50-5
Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$146In StockIn Stock
5 mg$350In StockIn Stock
10 mg$530In StockIn Stock
25 mg$859In StockIn Stock
50 mg$1,180In StockIn Stock
100 mg$1,590In StockIn Stock
500 mg$3,190-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.47%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.
In vivo
In acute experiments, Cronidipine was shown to be more potent than nifedipine and nicardipine in reducing blood pressure after i.v. and oral administration with less tachycardia. The hypotensive effects of Cronidipine (10 mg/kg) lasted for greater than 24 h, whereas the blood pressure-lowering effects of nifedipine and nicardipine (10 mg/kg) disappeared after 6 h. Cronidipinegiven orally once a day at 10 mg/kg for 14 days to spontaneously hypertensive rats, led to a marked and persistent decrease in blood pressure, with no significant changes in heart rate. In an attempt to prevent the development of hypertension, Cronidipine (3 and 10 mg/kg) was given once a day for 8 weeks to 5-week-old SHR. On the last day of treatment, Cronidipine had markedly reduced blood pressure over a 24 h period, however, there was no reduction of left ventricular hypertrophy, since body weight and left ventricular weight was not significantly different between control and treated groups.[2]
SynonymsLF-20254, LF20254, LF 20254, LF 2.0254
Chemical Properties
Molecular Weight598.04
FormulaC30H32ClN3O8
Cas No.113759-50-5
SmilesC(OCC1OC2(OC1)CCN(CC2)C3=CC=C(Cl)C=C3)(=O)C=4C(C(C(OC)=O)=C(C)NC4C)C5=CC(N(=O)=O)=CC=C5
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: 55 mg/mL (91.97 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6721 mL8.3606 mL16.7213 mL83.6064 mL
5 mM0.3344 mL1.6721 mL3.3443 mL16.7213 mL
10 mM0.1672 mL0.8361 mL1.6721 mL8.3606 mL
20 mM0.0836 mL0.4180 mL0.8361 mL4.1803 mL
50 mM0.0334 mL0.1672 mL0.3344 mL1.6721 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:
% DMSO
%
% Tween 80
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