Monoamine oxidase B inhibitors based on natural privileged scaffolds: A review of systematically structural modification

Y Lv, Z Zheng, R Liu, J Guo, C Zhang, Y Xie - International Journal of …, 2023 - Elsevier
Monoamine oxidase is a flavin enzyme that catalyzes the oxidation of monoamine
neurotransmitters in the brain. Various toxic by-products, aldehydes and hydrogen peroxide …

A review on biological and medicinal significance of thiazoles

PM Jadhav, S Kantevari, AB Tekale… - … , Sulfur, and Silicon …, 2021 - Taylor & Francis
Thiazole, a five-membered heterocyclic compound constitutes the skeleton of various
commercially marketed drug candidates and the heart-core in a diverse range of entities of …

Design, synthesis, mechanistic studies and in silico ADME predictions of benzimidazole derivatives as novel antifungal agents

MM Morcoss, MN El Shimaa, RA Ibrahem… - Bioorganic …, 2020 - Elsevier
Herein, novel three series of benzimidazole scaffold bearing hydrazone, 1, 2, 4-triazole and
1, 3, 4-oxadiazole moieties 1-3, 4a-j, 6a-c and 7 derivatives were designed, synthesized and …

Eco-friendly synthesis, characterization, in-silico ADMET and molecular docking analysis of novel carbazole derivatives as antibacterial and antifungal agents

O Merzouki, N Arrousse, A El Barnossi… - Journal of Molecular …, 2023 - Elsevier
In search of novel biologically potent compounds, three novel organic molecules have been
synthesized. The structures of the prepared compounds have been characterized by …

Synthesis of novel thiazolyl hydrazone derivatives as potent dual monoamine oxidase-aromatase inhibitors

AE Evren, D Nuha, S Dawbaa, BN Sağlık… - European journal of …, 2022 - Elsevier
The inhibitory effects of 2-thiazolyl hydrazones on monoamine oxidase enzymes are known
for a long time. In this study, a new series of 2-thiazolyl hydrazone derivatives were …

Design, synthesis and biological assessment of new selective COX-2 inhibitors including methyl sulfonyl moiety

BN Sağlık, D Osmaniye, S Levent, UA Çevik… - European Journal of …, 2021 - Elsevier
Nonsteroidal anti-inflammatory drugs (NSAIDs) cause peptic lesions in the gastrointestinal
mucosa by inhibiting the cyclooxygenase-1 (COX-1) enzyme. Selective COX-2 inhibition …

Expanding the anticancer potential of 1, 2, 3-triazoles via simultaneously targeting Cyclooxygenase-2, 15-lipoxygenase and tumor-associated carbonic anhydrases

PA Elzahhar, SM Abd El Wahab, M Elagawany… - European Journal of …, 2020 - Elsevier
Cancer is a multifactorial disorder involving multiplicity of interrelated signaling pathways
and molecular targets. To that end, a multi-target design strategy was adopted to develop …

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 …

Synthesis of new hydrazone derivatives and evaluation of their monoamine oxidase inhibitory activity

F Tok, BN Sağlık, Y Özkay, S Ilgın, ZA Kaplancıklı… - Bioorganic …, 2021 - Elsevier
A novel series of hydrazone derivatives were designed and synthesized. Their structures
were characterized by IR, 1 H NMR, 13 C NMR and HR-MS spectroscopic methods. The …