| Author | dc.contributor.author | Osorio Olivares, Mauricio | |
| Author | dc.contributor.author | Caroli Rezende, Marcos | es_CL |
| Author | dc.contributor.author | Sepúlveda Boza, Silvia | es_CL |
| Author | dc.contributor.author | Cassels Niven, Bruce | es_CL |
| Author | dc.contributor.author | Fierro, Angélica | es_CL |
| Admission date | dc.date.accessioned | 2012-06-06T19:17:19Z | |
| Available date | dc.date.available | 2012-06-06T19:17:19Z | |
| Publication date | dc.date.issued | 2004-05-26 | |
| Cita de ítem | dc.identifier.citation | Bioorganic & Medicinal Chemistry, Vol. 12, p. 4055–4066, 2004. | es_CL |
| Identifier | dc.identifier.issn | 0968-0896 | |
| Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/119464 | |
| Abstract | dc.description.abstract | Abstract—Twenty-nine arylisopropylamines, substituted at the b-position of their side chain by an oxo, hydroxy, or methoxy group,
were evaluated in vitro as MAO-A and MAO-B inhibitors. The oxo derivatives (‘cathinones’) were in general less active as MAO-A
inhibitors than the corresponding arylisopropylamines, but exhibited an interesting MAO-B inhibiting activity, which was absent in
the hydroxy, methoxy, and b-unsubstituted analogues. These results suggest that selective affinity for the two MAO isoforms in this
family of compounds is modulated not only by the aryl substitution pattern but also by the side-chain substituents on the arylalkylamine
scaffold. | es_CL |
| Patrocinador | dc.description.sponsorship | This work was supported by FONDECYT grant No.
1000776 and MECESUP-USA0007 project. | es_CL |
| Lenguage | dc.language.iso | en | es_CL |
| Publisher | dc.publisher | Elsevier Ltd. | es_CL |
| Keywords | dc.subject | Monoamine oxidase inhibition | es_CL |
| Título | dc.title | MAO inhibition by arylisopropylamines: the effect of oxygen substituents at the b-position | es_CL |
| Document type | dc.type | Artículo de revista | |
