Ontology highlight
ABSTRACT:
SUBMITTER: Fierro A
PROVIDER: S-EPMC4859490 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature
Fierro Angélica A Edmondson Dale E DE Celis-Barros Cristian C Rebolledo-Fuentes Marco M Zapata-Torres Gerald G
PloS one 20160506 5
Despite their structural and chemical commonalities, p-chloro-β-methylphenethylamine and p-methoxy-β-methylphenethylamine display distinct inhibitory and substrate activities upon MAO-B binding. Density Functional Theory (DFT) quantum chemical calculations reveal that β-methylation and para-substitution underpin the observed activities sustained by calculated transition state energy barriers, attained conformations and key differences in their interactions in the enzyme's substrate binding site. ...[more]