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Pravastatin sodium

Catalog No. T0672   CAS 81131-70-6
Synonyms: CS-514 Sodium, CS-514 (sodium)

Pravastatin sodium (CS-514 (sodium)), an HMG-CoA reductase inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM.

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Pravastatin sodium Chemical Structure
Pravastatin sodium, CAS 81131-70-6
Pack Size Availability Price/USD Quantity
10 mg In stock $ 40.00
25 mg In stock $ 55.00
50 mg In stock $ 66.00
100 mg In stock $ 101.00
200 mg In stock $ 130.00
500 mg In stock $ 215.00
1 mL * 10 mM (in DMSO) In stock $ 37.00
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Purity: 99.08%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Pravastatin sodium (CS-514 (sodium)), an HMG-CoA reductase inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM.
Targets&IC50 HMG-CoA reductase:5.6 μM
In vitro Pravastatin (30 mg/kg/day) reduced malnutrition-induced lesions by 34%. In female Wistar rats exposed to radiation, which presented with decreased CCN2 levels, Pravastatin (30 mg/kg/day) could restore muscle structure. A single dose of 40 mg of Pravastatin lowered cholesterol synthesis by 62% in monocytes from healthy individuals and by 47% in patients with hypercholesterolemia. Moreover, treatment with Pravastatin (40 mg/day for 8 weeks) in hypercholesterolemic patients increased LDL degradation by 57% while inhibiting cholesterol synthesis by 55%.
In vivo In murine peritoneal macrophages (MPM), the J-774 A.1 macrophage-like cell line, and human monocyte-derived macrophages (HMDM), Pravastatin exhibits a dose-dependent inhibition of cholesterol synthesis. Upon LDL addition, concentrations of Pravastatin below 0.19 μg/mL enhance the esterification of cellular cholesterol, whereas levels below 100 μg/mL suppress esterification. At less than 0.5 mM, Pravastatin attenuates the Rho/ROCK pathway activity in human ileal and colonic transplants, reducing CCN2 mRNA levels. Pravastatin at concentrations less than 1 mM also induces the inhibition of CCN2 in primary human smooth muscle cells. In all cases, Pravastatin at less than 0.5 mM reduces the mRNA levels of type I collagen and fibronectin. Pravastatin facilitates vasodilation in aortic rings, achieving 62.8% endothelium-dependent relaxation at 10 μM after 8 minutes. Pravastatin-Na at 10 μM inhibits sterol synthesis with 50% greater efficacy than in peripheral blood mononuclear cells. In bovine aortic endothelial cells, Pravastatin at less than 10 μM stimulates NOS activity and NO release within 10 minutes, with L-arginine further enhancing NO production in response to Pravastatin.
Synonyms CS-514 Sodium, CS-514 (sodium)
Molecular Weight 446.52
Formula C23H35NaO7
CAS No. 81131-70-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 44.7 mg/mL (100 mM)

DMSO: 44.7 mg/mL (100 mM)

TargetMolReferences and Literature

1. Kurakata S, et al. Immunopharmacology, 1996, 34(1), 51-61. 2. Kaesemeyer WH, et al. J Am Coll Cardiol, 1999, 33(1), 234-241. 3. Keidar S, et al. Br J Clin Pharmacol, 1994, 38(6), 513-519. 4. Haydont V, et al. Clin Cancer Res, 2007, 13(18 Pt 1), 5331-5340. 5. Dagli N, et al. Inflammation, 2007, 30(6), 230-235. 6. Huang Y, Zucker B, Zhang S, et al. Migrasome formation is mediated by assembly of micron-scale tetraspanin macrodomains[J]. Nature cell biology. 2019, 21(8): 991.

TargetMolCitations

1. Huang Y, Zucker B, Zhang S, et al. Migrasome formation is mediated by assembly of micron-scale tetraspanin macrodomains. Nature cell biology. 2019, 21(8): 991.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Anti-Cancer Clinical Compound Library Anti-Cancer Approved Drug Library Microbial Natural Product Library Anti-Cancer Drug Library Inhibitor Library Anti-Cancer Metabolism Compound Library Drug-induced Liver Injury (DILI) Compound Library Bioactive Lipid Compound Library Orally Active Compound Library

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Keywords

Pravastatin sodium 81131-70-6 Apoptosis Autophagy Metabolism Ferroptosis HMG-CoA Reductase Pravastatin CS514 HMG-CoA Reductase (HMGCR) inhibit Inhibitor CS 514 CS-514 Sodium CS-514 (sodium) CS-514 inhibitor

 

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