High purity pravastatin sodium epastatinsodium 81131-70-6 factory
Basic information
Product Name: |
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Synonyms: |
1-naphthaleneheptanoicacid,1,2,6,7,8,8a-hexahydro-2-methyl-8-(2-methyl-1-oxob;2-alpha,6-alpha,8-beta(r*),8a-alpha))-*;cs-514;epastatinsodium;lipostat;sq31000;utoxy)-beta,delta,6-trihydroxy-,monosodiumsalt,(1s-(1-alpha(beta-s*,delta-s;KOPOSTAT |
CAS: |
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MF: |
C23H36NaO7 |
MW: |
447.52 |
Product Categories: |
Active Pharmaceutical Ingredients;Antihyperlipoproteinemic;Various Metabolites and Impurities;Chiral Reagents;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;HMG-CoA reductase;Inhibitor;PRAVACHOL |
Mol File: |
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Chemical Properties |
melting point |
171.2-173 °C |
boiling point |
634.5 °C at 760 mmHg |
flashing point |
213.2 °C |
vapor pressure |
9.15E-19 mmHg at 25 °C |
storage temp. |
2-8°C |
solubility |
H2O: 19 mg/mL |
Usage And Synthesis |
Chemical Properties |
White Crystalline Powder |
Usage |
A competitive inhibitor of HMG-CoA reductase. Bioactive metabolite of Mevastatin |
antihyperlipidemic, HMGCoA reductase inhibitor |
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Pravastatin sodium is the salt of pravastatin, a ring-opened member of the statin family. Pravastatin is produced biosynthetically from compactin (mevastatin) by a number of microorganisms, notably Absidia, Cunninghamella, Syncephalastrum, Nocardia or Streptomyces. Typically, statins like compactin, lovastatin and simvastatin possess a β-hydroxy lactone ring which is a pro-drug for the readily ring-opened dihydroxyacid generally regarded as the active HMG-CoAreductase inhibitor. Importantly, the free carboxylic acid enables pravastatin to be freely water soluble within biological pH ranges. |
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An HMGCR inhibitor which blocks cholesterol synthesis |
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Biological Activity |
Water-soluble, competitive inhibitor of 3-hydroxy-3-methyl coenzyme A (HMG-CoA) reductase. Potently blocks cholesterol synthesis in vivo (K i ~ 1 nM) and displays cardioprotective properties. |
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