CAS 42058-59-3
:Acétate de méthyle (3-hydroxyphényl)
- 3-Hydroxyphenylaceticacidmethylester
- Benzeneacetic acid, 3-hydroxy-, methyl ester
- Methyl 3-Hydroxyphenylacetate
- Methyl m-hydroxyphenylacetate
- 3-Hydroxyphenylacetic Acid Methyl Ester
3-Hydroxyphenylacetic acid methyl ester
CAS :Formule :C9H10O3Degré de pureté :98%Couleur et forme :LiquidMasse moléculaire :166.1739Methyl 2-(3-hydroxyphenyl)acetate
CAS :Methyl 2-(3-hydroxyphenyl)acetateDegré de pureté :98%Masse moléculaire :166.17g/molMethyl 3-Hydroxyphenylacetate
CAS :Formule :C9H10O3Degré de pureté :>98.0%(GC)Couleur et forme :Colorless to Light orange to Yellow clear liquidMasse moléculaire :166.18Methyl 2-(3-hydroxyphenyl)acetate
CAS :Formule :C9H10O3Degré de pureté :98%Couleur et forme :LiquidMasse moléculaire :166.176Methyl 3-Hydroxyphenylacetate
CAS :Formule :C26H27ClO10Couleur et forme :NeatMasse moléculaire :534.94(3-Hydroxyphenyl)acetic acid methyl ester
CAS :(3-Hydroxyphenyl)acetic acid methyl ester is an allosteric inhibitor of the serotonin transporter (SERT), which is a target enzyme for many drugs. It has inhibitory activity against 5-HT1A receptors, and other targets that have not yet been elucidated. This compound has been shown to react with coumarin derivatives to form reaction products. The molecular modelling of this drug shows that its uptake is inhibited by the presence of acids, such as hydrochloric acid, in the environment. The rate of reaction between (3-hydroxyphenyl)acetic acid methyl ester and serotonin has been determined experimentally using kinetic data. Molecular modeling predicts that this compound will bind tightly to the SERT protein via hydrogen bonding interactions with amino acids in the binding site.
Formule :C9H10O3Degré de pureté :Min. 95%Couleur et forme :Colorless PowderMasse moléculaire :166.17 g/mol





