Development of piperic acid-based monoamine oxidase inhibitors: Synthesis, structural characterization and biological evaluation

• Type: Article in International Scientific Journal
• Date: 2019

Authors

Chavarria, D (Author) Other; Fernando Cagide (Author) FCUP; Pinto, M (Author) Other; Gomes, LR (Author) Other; Low, JN (Author) Other; Fernanda Borges (Author) FCUP

Journal

Title: Journal of Molecular Structure

Vol. 1182

Pages: 298-307

ISSN: 0022-2860

Publisher: Elsevier

Indexing

Scopus - 5 Citations

Other information

Authenticus ID: P-00S-6Q2

DOI: 10.1016/j.molstruc.2019.01.060

Abstract (EN): A series of piperic acid esters and amides were synthesized using a two-step strategy. Mass spectrometry and unidimensional ( 1 H NMR, 13 C NMR, DEPT) and bidimensional (COSY, HSQC, HMBC) NMR methodologies were used to study the molecular structure of the final compounds, resulting in the assignment of all detected signals. Preliminary biological data of piperine and the derivatives thereof showed that piperic acid 2 and amides 3 and 4 did not display significant inhibitory activity at 10 ¿M against both hMAO-A and hMAO-B. In contrast, the esters 5 and 6 displayed relevant hMAO inhibitory activities, with IC 50 values for hMAO-B lower than piperine and within the nanomolar range (compound 1: IC 50 = 1.05 ¿M; compound 6: IC 50 = 169 nM; compound 5: IC 50 = 156 nM). Moreover, X-ray crystallographic analyses showed relevant differences between amides 3 and 4 and esters 5 and 6 constituting a valuable information to understand the ligand-target interactions. Additional studies are warranted for a systematic lead optimization process that can lead in the future to a more potent and selective hMAO-B inhibitor based on piperine scaffold. © 2019 Elsevier B.V.

Language: English

Type (Professor's evaluation): Scientific