Inhibition of monoamine oxidase by selected C5- and C6-substituted isatin analogues
作者:Clarina I. Manley-King、Jacobus J. Bergh、Jacobus P. Petzer
DOI:10.1016/j.bmc.2010.11.028
日期:2011.1
are reversible inhibitors of human monoamineoxidase (MAO) A and B. Both homologues are reported to exhibit selective binding to the MAO-B isoform with (E)-5-styrylisatin being the most potent inhibitor. To further investigate these structure–activity relationships (SAR), in the present study, additional C5- and C6-substituted isatinanalogues were synthesized and evaluated as inhibitors of recombinant