Novel inhibitors of cholinesterases, especially butyrylcholinesterase(BuChE), were obtained by coupling melatonin-tacrine heterodimersvia the carbamate bond. Compounds 14a-i possessed potent cholinesterase inhibitory activity (with IC50 values as low as 1.18 nM for acetylcholinesterase (AChE) and 0.24 nM for butyrylcholinesterase (BuChE)). These heterodimers exhibit selectivity toward BuChE, being from 4- to 256-fold more active toward BuChE than AChE, but still acting as better AChE inhibitors than tacrine 4. [ABSTRACT FROM AUTHOR]