Pitavastatin calcium [147526-32-7]

Référence T2534-25mg

Conditionnement : 25mg

Marque : TargetMol

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Pitavastatin calcium

(Synonyms: Pitavastatin hemicalcium, P-872441, NK-104 hemicalcium) Copy Product Info
Pitavastatin calcium (NK-104) is a potent inhibitor of HMG-CoA reductase (Ki: 1.7 nM). It lowers both total cholesterol and low-density lipoprotein cholesterol in animals and humans. Metabolism of pitavastatin by the cytochrome P450 system is minimal, reducing the risk of drug-drug interactions.
Pitavastatin calcium
Cas No. 147526-32-7
For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.49%
Color:White
COA HNMR LCMS

Product Introduction

Bioactivity
Description
Pitavastatin calcium (NK-104) is a potent inhibitor of HMG-CoA reductase (Ki: 1.7 nM). It lowers both total cholesterol and low-density lipoprotein cholesterol in animals and humans. Metabolism of pitavastatin by the cytochrome P450 system is minimal, reducing the risk of drug-drug interactions.
Targets & IC50
HMG-CoA:5.8 nM
In vivo
Pitavastatin inhibits the progression of arterial atherosclerosis by blocking the synthesis of thromboxane and suppressing the migration or proliferation of vascular smooth muscle induced by angiotensin II, thereby stabilizing atherosclerotic plaques. It significantly reduces the levels of intracellular and synthesized cholesteryl esters. Moreover, pitavastatin enhances the extracellular expression of LDL receptors and increases the binding of LDL to LDL receptors. Compared to simvastatin and atorvastatin, pitavastatin is more effective in inducing the expression of LDL receptor mRNA.
SynonymsPitavastatin hemicalcium, P-872441, NK-104 hemicalcium
Chemical Properties
Molecular Weight880.98
FormulaC50H46CaF2N2O8
Cas No.147526-32-7
Smiles[Ca++].O[C@H](C[C@H](O)\C=C\c1c(nc2ccccc2c1-c1ccc(F)cc1)C1CC1)CC([O-])=O.O[C@H](C[C@H](O)\C=C\c1c(nc2ccccc2c1-c1ccc(F)cc1)C1CC1)CC([O-])=O
Relative Density.no data available
Storage & Solubility Information
StorageKeep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 250 mg/mL (283.77 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 10 mg/mL (11.35 mM), Solution.
10% DMSO+90% Saline: < 10 mg/mL (11.35 mM), Lower concentrations may be soluble, but exact solubility limit is unknown.
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 mM1.1351 mL5.6755 mL11.3510 mL56.7550 mL
5 mM0.2270 mL1.1351 mL2.2702 mL11.3510 mL
10 mM0.1135 mL0.5675 mL1.1351 mL5.6755 mL
20 mM0.0568 mL0.2838 mL0.5675 mL2.8377 mL
50 mM0.0227 mL0.1135 mL0.2270 mL1.1351 mL
100 mM0.0114 mL0.0568 mL0.1135 mL0.5675 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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