SML0038
Fluvastatin sodium hydrate
≥98% (HPLC)
Synonym(s):
(±)-(3R*,5S*,6E)-7-[3-(4-Fluorophenyl)-1-(1-methyethyl)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid sodium salt hydrate
About This Item
Recommended Products
Assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to tan
solubility
H2O: ≥9 mg/mL
originator
Novartis
storage temp.
2-8°C
SMILES string
O.[Na+].CC(C)n1c(\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O)c(-c2ccc(F)cc2)c3ccccc13
InChI
1S/C24H26FNO4.Na.H2O/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30;;/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30);;1H2/q;+1;/p-1/b12-11+;;/t18-,19-;;/m1../s1
InChI key
KKEMYLLTGGQWCE-PMRANXHDSA-M
Application
- to examine its effect on β -glucan-induced training on immunity
- to investigate the effect of statins on the number of uncoupling protein 1 (UCP1)+ cells
- to determine its effect on insulin degrading enzyme (IDE) secretion from astrocytes
- to treat and study its effect on human umbilical vein endothelial cells (HUVECs) in vitro
- to test its anti-hepatitis C virus (HCV) activity
- as a cholesterol inhibitor
- to study its effects on β-glucan-induced monocyte immune training
Biochem/physiol Actions
Features and Benefits
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
Randomized controlled clinical studies have suggested 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors (statins) are effective in both primary and secondary prevention of cardiovascular disease (CVD) events.
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