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Synthesis and molecular docking studies of imines as α-glucosidase and α-amylase inhibitors.

Abstract：

:Imine functionality is found in many compounds with important biological activity. Thus, the development of novel synthetic approaches for imines is important. In this work, it is propose an easy, eco-friendly and straightforward synthesis pathway of aryl imines under microwave irradiation catalyzed by Alumina-sulfuric acid. In addition, the in vitro enzymatic inhibition, antioxidant activity and molecular docking studies were performed. The aryl imines were isolated with yields in the range of 37-94%. All aryl imines synthesized were evaluated for in vitro inhibitory potential against α-glucosidase and α-amylase enzymes and the results exhibited that the most of the compounds displayed inhibitory activity against both enzymes. The (E)-1-(4-nitrophenyl)-N-(pyridin-2-yl)methanimine (3d) was 1.15-fold more active than acarbose against α-amylase whilst the (E)-1-phenyl-N-(pyridin-2-yl)methanimine (3c) displayed similar activity that acarbose against α-glucosidase. The molecular docking studies in α-glucosidase and α-amylase reveal that aryl imines mainly establish an H-bond with the R2-subtituent and hydrophobic interactions with the R1-subtituent. The docking analysis reveals these synthetic aryl imines 3d-i interact in same active site than acarbose drug in both enzymes.

journal_name

Bioorg Chem

journal_title

Bioorganic chemistry

authors

Aispuro-Pérez A,López-Ávalos J,García-Páez F,Montes-Avila J,Picos-Corrales LA,Ochoa-Terán A,Bastidas P,Montaño S,Calderón-Zamora L,Osuna-Martínez U,Sarmiento-Sánchez JI

doi

10.1016/j.bioorg.2019.103491

subject

Has Abstract

pub_date

2020-01-01 00:00:00

pages

103491

eissn

0045-2068

issn

1090-2120

pii

S0045-2068(19)31327-6

journal_volume

94

pub_type

杂志文章

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