Privileged scaffolds as MAO inhibitors: Retrospect and prospects

AC Tripathi, S Upadhyay, S Paliwal, SK Saraf - European Journal of …, 2018 - Elsevier
This review aims to be a comprehensive, authoritative, critical, and readable review of
general interest to the medicinal chemistry community because it focuses on the …

MAO enzymes inhibitory activity of new benzimidazole derivatives including hydrazone and propargyl side chains

ÖD Can, D Osmaniye, ÜD Özkay, BN Sağlık… - European journal of …, 2017 - Elsevier
In the present work, 15 new N'-(arylidene)-4-(1-(prop-2-yn-1-yl)-1H-benzo [d] imidazol-2-yl)
benzohydrazide (4a-4o) were designed and synthesized. The structures of the synthesized …

Importance of indazole against neurological disorders

D Pal, P Sahu - Current Topics in Medicinal Chemistry, 2022 - ingentaconnect.com
Indazole is a nitrogen-containing bicyclic compound, having three tautomeric forms:
1Hindazole, 2H-indazole, and 3H-indazole. Mostly, they are considered as 1H-indazole …

Design, Synthesis, and In Vitro and In Silico Approaches of Novel Indanone Derivatives as Multifunctional Anti-Alzheimer Agents

BN Sağlık, S Levent, D Osmaniye, AE Evren… - ACS …, 2022 - ACS Publications
Alzheimer's disease (AD) is a neurological, progressive illness that typically affects the
elderly and is clinically distinguished by memory and cognitive decline. Due to a number of …

In vitro and in silico evaluation of new thiazole compounds as monoamine oxidase inhibitors

BN Sağlık, BK Çavuşoğlu, D Osmaniye, S Levent… - Bioorganic …, 2019 - Elsevier
New twenty compounds bearing thiazole ring (3a-3t) were designed and synthesized as
monoamine oxidase (MAO) inhibitors. The fluorometric enzyme inhibition assay was used to …

Design, synthesis and biological assessment of new thiazolylhydrazine derivatives as selective and reversible hMAO-A inhibitors

NÖ Can, D Osmaniye, S Levent, BN Sağlık… - European journal of …, 2018 - Elsevier
In the recent works, it was shown that numerous thiazolylhydrazine derivatives display h
MAO inhibitory activity in the range of micromolar concentration. Hence, in the present study …

Synthesis of new hydrazone derivatives for MAO enzymes inhibitory activity

NÖ Can, D Osmaniye, S Levent, BN Sağlık, B Inci… - Molecules, 2017 - mdpi.com
In the present work, 14 new 1-substituted-2-phenylhydrazone derivatives were synthesized
to evaluate their inhibitory activity against h MAO enzymes. The structures of the newly …

Combining QSAR classification models for predictive modeling of human monoamine oxidase inhibitors

AM Helguera, A Pérez-Garrido, A Gaspar, J Reis… - European journal of …, 2013 - Elsevier
Due to their role in the metabolism of monoamine neurotransmitters, MAO-A and MAO-B
present a significant pharmacological interest. For instance the inhibitors of human MAO-B …

Design and Synthesis of New Benzothiazole Compounds as Selective hMAO-B Inhibitors

S Ilgın, D Osmaniye, S Levent, BN Sağlık, U Acar Çevik… - Molecules, 2017 - mdpi.com
In the current work a new class of novel benzothiazole-hydrazone derivatives was designed
and synthesized as h MAO-B inhibitors. Structures of the obtained compounds (3a–3j) were …

Design, Synthesis, and Biological Effect Studies of Novel Benzofuran–Thiazolylhydrazone Derivatives as Monoamine Oxidase Inhibitors

D Osmani̇ye, BN Sağlik, S Levent, UA Çevi̇k… - ACS …, 2024 - ACS Publications
In recent studies, monoamine oxidase (MAO) inhibitory effects of various thiazolylhydrazone
derivatives have been demonstrated. Within the scope of this study, 12 new compounds …