LOVASTATIN-D9

LOVASTATIN-D9 Suppliers list
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Company Name: Manhag Testing Technology Co., Ltd  
Tel: 400-818 0104 18918165978
Email: zilin.ren@bestown.net.cn
Company Name: TargetMol  
Tel: 400-821-0310 15002144251
Email: xuexiang.shao@tsbiochem.com
LOVASTATIN-D9 Basic information
Product Name:LOVASTATIN-D9
Synonyms:LOVASTATIN-D9;Lovastatin-[D9] (Standard)
CAS:1002346-03-3
MF:C24H36O5
MW:404.55
EINECS:
Product Categories:
Mol File:Mol File
LOVASTATIN-D9 Structure
LOVASTATIN-D9 Chemical Properties
solubility Chloroform: slightly soluble
Methanol: slightly soluble
Safety Information
MSDS Information
LOVASTATIN-D9 Usage And Synthesis
DescriptionLovastatin-d9 is intended for use as an internal standard for the quantification of lovastatin (Item No. 10010338) by GC- or LC-MS. Lovastatin is a fungal metabolite that has been found in A. terreus and an inhibitor of HMG-CoA reductase (Ki = 1.4 nM).1,2 It is also a prodrug form of the HMG-CoA reductase inhibitor lovastatin hydroxy acid (Item No. 10010339).2 Lovastatin (8 mg/kg per day) reduces plasma cholesterol levels in dogs. It suppresses TNF-induced NF-κB activation (IC50 = ~15 µM) and potentiates apoptosis in human myeloid leukemia cells.3 Lovastatin also increases cellular lipid peroxidation and decreases glutathione peroxidase 4 (GPX4) levels in cancer cells.4 Formulations containing lovastatin have been used in the treatment of hypercholesterolemia.WARNING This product is not for human or veterinary use.
References[1] ENDO A. The discovery and development of HMG-CoA reductase inhibitors.[J]. Journal of Lipid Research, 1992, 33 11: 1569-1582.
[2] A W ALBERTS. Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1980, 77 7: 3957-3961. DOI: 10.1073/pnas.77.7.3957
[3] KWANG SEOK AHN  Bharat B A  Gautam Sethi. Reversal of chemoresistance and enhancement of apoptosis by statins through down-regulation of the NF-κB pathway[J]. Biochemical pharmacology, 2008, 75 4: Pages 907-913. DOI: 10.1016/j.bcp.2007.10.010
[4] VASANTHI S. VISWANATHAN. Dependency of a therapy-resistant state of cancer cells on a lipid peroxidase pathway[J]. Nature, 2017, 547 7664: 453-457. DOI: 10.1038/nature23007
LOVASTATIN-D9 Preparation Products And Raw materials
Tag:LOVASTATIN-D9(1002346-03-3) Related Product Information
Lovastatin SIMVASTATIN-D6 Lovastatin sodium salt Simvastatin ammonium salt sodium:(3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-[(2S)-2-(trideuteriomethyl)butanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate