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Authordc.contributor.authorLühr-Sierra, Susan 
Authordc.contributor.authorVilches-Herrera, Marcelo es_CL
Authordc.contributor.authorFierro, Angélica es_CL
Authordc.contributor.authorRamsay, Rona es_CL
Authordc.contributor.authorEdmondson, Dale E. es_CL
Authordc.contributor.authorReyes Parada, Miguel es_CL
Authordc.contributor.authorCassels Niven, Bruce es_CL
Authordc.contributor.authorIturriaga-Vásquez, Patricio es_CL
Admission datedc.date.accessioned2010-07-19T20:54:48Z
Available datedc.date.available2010-07-19T20:54:48Z
Publication datedc.date.issued2010
Cita de ítemdc.identifier.citationBioorganic & Medicinal Chemistry 18 (2010) 1388–1395en_US
Identifierdc.identifier.otherdoi:10.1016/j.bmc.2010.01.029
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119080
Abstractdc.description.abstract2-Arylthiomorpholine and 2-arylthiomorpholin-5-one derivatives, designed as rigid and/or non-basic phenylethylamine analogues, were evaluated as rat and human monoamine oxidase inhibitors. Molecular docking provided insight into the binding mode of these inhibitors and rationalized their different potencies. Making the phenylethylamine scaffold rigid by fixing the amine chain in an extended six-membered ring conformation increased MAO-B (but not MAO-A) inhibitory activity relative to the more flexible amethylated derivative. The presence of a basic nitrogen atom is not a prerequisite in either MAO-A or MAO-B. The best Ki values were in the 10 8 M range, with selectivities towards human MAO-B exceeding 2000-fold.en_US
Patrocinadordc.description.sponsorshipThis work was partially funded by FONDECYT Grants 1060199, 1090037, 11085002, PBCT PDA-23 and ICM Grant P05-001-F. S.L. was the recipient of a CONICYT scholarship and a MeceSup travel grant. The authors thank Mr. Marco Rebolledo-Fuentes for expert experimental support. D.E.E. acknowledges support from NIH Grant GM-29433 and technical assistance from Ms. Milagros Aldeco in purifying the recombinant human MAOB used in this study.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherELSEVIERen_US
Keywordsdc.subjectMonoamine oxidaseen_US
Títulodc.title2-Arylthiomorpholine derivatives as potent and selective monoamine oxidaseen_US
Document typedc.typeArtículo de revista


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