2-Bromo-3'-methoxyacetophenone

CAS : 5000-65-7

Ref. 3D-FB19124

Informations sur le produit

• Nom: 2-Bromo-3'-methoxyacetophenone
• Synonymes: 3'-Methoxyphenacyl bromide2-Bromo-1-(3-methoxyphenyl)ethanone3-Methoxyphenacyl bromide, 2-Bromo-1-(3-Methoxyphenyl)Ethanone, 2-Bromo-1-(3-methoxyphenyl)ethan-1-one, 2-Bromo-1-(3-methoxyphenyl-1-yl)ethanone, 2-Bromo-1-[3-(methyloxy)phenyl]ethanone, 2-Bromo-3-methoxyacotophenone, 2-Bromo-m-methoxyacetophenone, 3-Methoxyphenacyl bromide, Acetophenone, 2-bromo-3′-methoxy-, Bromomethyl 3-Methoxyphenyl Ketone, Ethanone, 2-bromo-1-(3-methoxyphenyl)-, NSC 405833, alpha-Bromo-3-methoxyacetophenone, m-(Bromoacetyl)anisole, m-Methoxyphenacyl bromide, α-Bromo-3′-methoxyacetophenone, α-Bromo-m-methoxyacetophenone, ω-Bromo-3-methoxyacetophenone

Description

2-Bromo-3'-methoxyacetophenone is a reactive compound that has been used as an antiplatelet drug. It is a prodrug of vicagrel, which inhibits the platelet aggregation by blocking the conversion of ADP to ATP. It also has been shown to inhibit the growth of cryptococcus neoformans. This compound binds to matrix proteins and disrupts their structure, leading to a decrease in platelet adhesion. 2-Bromo-3'-methoxyacetophenone has been shown to be metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. The biological properties of this drug are complex and depend on its concentration and duration of exposure. Its effect on platelet aggregation is due to its ability to inhibit the activity of protein kin

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 229.07 g/mol
• Formule: C₉H₉BrO₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C9H9BrO2/c1-12-8-4-2-3-7(5-8)9(11)6-10/h2-5H,6H2,1H3
• Code InChI: InChIKey=IOOHBIFQNQQUFI-UHFFFAOYSA-N
• SMILES: COc1cccc(C(=O)CBr)c1