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Human and rat monoamine oxidase-A are differentially inhibited by (S)-4-alkylthioamphetamine derivatives. Insights from molecular modeling studies

Four enantiomerically pure (S)-4-alkylthioamphetamine derivatives were evaluated as monoamine oxidase (MAO) inhibitors using the human and rat isoforms of the enzyme. Molecular dockings were performed in order to gain insights regarding the binding mode of these inhibitors. All compounds were potent...

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Autors principals: Fierro, Angélica, Osorio-Olivares, Mauricio, Cassels, Bruce K., Edmondson, Dale E., Sepúlveda-Boza, Silvia, Reyes-Parada, Miguel
Format: Artigo
Idioma:Inglês
Publicat: 2007
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1949415/
https://ncbi.nlm.nih.gov/pubmed/17521909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2007.05.021
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