Entacapone (sodiuM salt)

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Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Entacapone sodium salt
CAS:1047659-02-8
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354;
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Products Intro: Product Name:Entacapone sodium salt
CAS:1047659-02-8
Package:50mg;1980USD|25mg;1520USD|100mg;2500USD
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Entacapone sodium salt
CAS:1047659-02-8
Package:50mg;1980USD|25mg;1520USD|100mg;2500USD
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:Entacapone Sodium
CAS:1047659-02-8
Purity:0.97 Package:mgs,gs,kgs Remarks:A922031
Company Name: MedChemexpress LLC  
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Products Intro: Product Name:Entacapone (sodium salt)
CAS:1047659-02-8
Purity:>98% Package:600RMB/10mg

Entacapone (sodiuM salt) manufacturers

Entacapone (sodiuM salt) Basic information
Product Name:Entacapone (sodiuM salt)
Synonyms:Entacapone (sodiuM salt);Entacapone Sodium;Sodium (E)-4-(2-cyano-3-(diethylamino)-3-oxoprop-1-en-1-yl)-2-hydroxy-6-nitrophenolate
CAS:1047659-02-8
MF:C14H14N3NaO5
MW:329.29
EINECS:
Product Categories:
Mol File:1047659-02-8.mol
Entacapone (sodiuM salt) Structure
Entacapone (sodiuM salt) Chemical Properties
solubility Soluble in DMSO
form Powder
Safety Information
MSDS Information
Entacapone (sodiuM salt) Usage And Synthesis
UsesEntacapone sodium salt is a potent, reversible, peripherally acting and orally active catechol-O-methyltransferase (COMT) inhibitor. Entacapone sodium salt inhibits COMT from rat brain, erythrocytes and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone sodium salt is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC50s>50 μM). Entacapone sodium salt can be used for the research of Parkinson's disease[1]. Entacapone sodium salt serves as as a inhibit of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders[2].
in vivo

Entacapone sodium salt (oral administration; 600 mg/kg per day; 3-9 weeks) results in a dose-response effect dose-response effect. After 3 weeks, mouse body weight are decreased by 10.1% compared to controls, and shows similar food intake??fat mass and fat mass ratio reduced after Entacapone sodium salt treatment. Entacapone sodium salt also increases the energy expenditure of mice: reductions in total cholesterol (17.6%), low-density lipoprotein cholesterol (31.0%), and triglycerides (10.2%) in mice[2].

References[1] E Nissinen, et al. Biochemical and pharmacological properties of a peripherally acting catechol-O-methyltransferase inhibitor Entacapone sodium salt . Naunyn Schmiedebergs Arch Pharmacol. 1992 Sep;346(3):262-6. DOI:10.1007/BF00173538
[2] Shiming Peng, et al. Identification of Entacapone sodium salt as a chemical inhibitor of FTO mediating metabolic regulation through FOXO1. Sci Transl Med DOI:10.1126/scitranslmed.aau7116
Entacapone (sodiuM salt) Preparation Products And Raw materials
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