Simvastatin
Chemical Name: (1S,3R,7S,8S,8aR)-1,2,3,7,8,8a-Hexahydro-3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyly-2,2-dimethyl butanoate
Purity: ≥98%
Biological Activity
Simvastatin is a HMG-CoA reductase inhibitor; decreases levels of low density lipoprotein. Simvastatin is also an AMPK activator. Has multiple biological effects including bone formation stimulation, inhibition of smooth muscle cell proliferation and migration, induction of ferroptosis, inhibition of autophagy, and anticancer and anti-inflammatory activity. Inactive lactone prodrug of simvastatin hydroxy acid, naturally bioactivated in vivo following oral administration.Simvastatin acts synergistically with ABL allosteric inhibitors GNF 5 (Cat. No. 1965) to enhance apoptosis of metastatic lung cancer cells in mice.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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Apigenin in the regulation of cholesterol metabolism and protection of blood vessels
K Zhang, W Song, D Li, X Jin
Exp Ther Med, 2017;13(5):1719-1724. -
STAT and bone formation.
Garrett et al.
Curr.Pharm.Des., 2001;7:715 -
Potential anticancer effects of STAT: fact or fiction?
Kaushal et al.
Endothelium, 2003;10:49 -
Pharmacological effects of HMG CoA reductase inhibitors other than lipoprotein modulation.
White
J.Clin.Pharmacol., 1999;39:111 -
Preclinical pharmacokinetics of STAT.
Reinoso et al.
Methods Find.Exp.Clin.Pharmacol., 2002;24:593
Product Datasheets
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Citations for Simvastatin
The citations listed below are publications that use Tocris products. Selected citations for Simvastatin include:
4 Citations: Showing 1 - 4
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Chemical and genetic validation of the statin drug target to treat the helminth disease, schistosomiasis.
Authors: Rojo-Arreola Et al.
PLoS One 2014;9:e87594
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Acute SimV. inhibits K ATP channels of porcine coronary artery myocytes.
Authors: Seto Et al.
Br J Pharmacol 2013;8:e66404
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Phospholipase PLA2G7, associated with aggressive prostate cancer, promotes prostate cancer cell migration and invasion and is inhibited by STAT.
Authors: Vainio Et al.
Pharmacol Res Perspect 2011;2:1176
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Modulation by SimV. of iberiotoxin-sensitive, Ca2+-activated K+ channels of porcine coronary artery smooth muscle cells.
Authors: Seto Et al.
Oncotarget 2007;151:987
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