Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Development of Fluorinated Thienylchalcones as Monoamine Oxidase-B Inhibitors: Design, Synthesis, Biological Evaluation and Molecular Docking Studies

Author(s): Bijo Mathew, Gulberk Ucar, Samiye Yabanogclu-Ciftci, Ipek Baysal, Jerad Suresh, Githa Elizabeth Mathew, Jobin Kunjumon Vilapurathu, A. M. Nadeena, P. Nabeela, V. Lakshmi, Abitha Haridas and Fajeelath Fathima

Volume 12 , Issue 9 , 2015

Page: [605 - 613] Pages: 9

DOI: 10.2174/1570178612666150903213416

Price: $65

Abstract

A series of thienylchalcones with fluoro and trifluoromethyl derivatives were synthesized and evaluated for their capability to inhibit human monoamine oxidase A and B. The chemical structures of the compounds have been ascertained by means of their 1HNMR, 13CNMR, mass spectroscopic data and elemental analysis. The results documented that these compounds revealed moderate to good inhibitory activities towards MAO-B than MAO-A. The most active compound, (2E)-1-(thiophen-2-yl)-3-[4-(trifluoromethyl) phenyl] prop-2-en-1-one exhibited with Ki value for MAO-B of 0.90 ± 0.05 µM with a 5-fold selectivity for MAO-B over the MAO-A isoform. All the fluorinated thienylchalcones under the present study showed as reversible inhibitors, while kinetic analysis revealed a competitive mode of binding. Molecular docking studies were executed to further explain the in vitro results of the new compounds, and to establish the hypothetical binding poses for the compounds inside the inhibitor binding cavity of hMAO-B.

Keywords: 2-Acetyl thiophene, docking, MAO-B, reversible inhibition, thienylchalcones.

Graphical Abstract

Rights & Permissions Print Export Cite as
© 2022 Bentham Science Publishers | Privacy Policy