Synthesis and structure–activity relationships of serotonin derivatives effect on α-glucosidase inhibition

Medicinal Chemistry Research
2012.0

Abstract

The a-glucosidase inhibitory activities of serotonin derivatives were evaluated. Two serotonin derivatives, N-p-coumaroyl serotonin (2) and N-caffeoyl serotonin (4) exhibited most potent inhibition on a-glucosidase, whereas, cinnamic acid derivatives were less efficient. Furthermore, we analyzed their structural importance for a-glucosidase inhibition. The linkage of cinnamic acid moiety and serotonin moiety and the olefin in cinnamic acid moiety of serotonin derivatives were crucial for a-glucosidase inhibition. This is the first report on structure–activity relationships (SAR) for the a-glucosidase inhibitory activity of serotonin derivatives.

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