The
search for new drugs fulfilling One Health and Green Chemistry
requirements is an urgent call. Here, for the first time, we envisaged
developing SAHA analogues by starting from the cashew nutshell liquid
(CNSL) agro-industrial waste and employing a metathesis approach.
This sustainable combination (comprising principles #7 and #9) allowed
a straightforward synthesis of compounds 13–20. All of them were found to not be toxic on HepG2, IMR-32,
and L929 cell lines. Then, their potential against major human and
animal vector-borne parasitic diseases (VBPDs) was assessed. Compound 13 emerged as a green hit against the trypomastigote forms
of T. b. brucei. In silico studies
showed that the T. b. brucei HDAC (TbDAC) catalytic
pocket could be occupied with a similar binding mode by both SAHA
and 13, providing a putative explanation for its antiparasitic
mechanism of action (13, EC50 = 0.7 ±
0.2 μM).