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 …

Advances in the discovery of heterocyclic-based drugs against Alzheimer's disease

JD Sánchez, AR Alcántara, JF González… - Expert Opinion on …, 2023 - Taylor & Francis
Introduction Alzheimer's disease is a multifactorial neurodegenerative disorder
characterized by beta-amyloid accumulation and tau protein hyperphosphorylation. The …

Multicomponent Petasis reaction for the identification of pyrazine based multi-target directed anti-Alzheimer's agents: In-silico design, synthesis, and characterization

H Madhav, SA Abdel-Rahman, MA Hashmi… - European Journal of …, 2023 - Elsevier
Multi-target directed ligands (MTDLs) have recently attracted significant interest due to their
exceptional effectiveness against multi-factorial Alzheimer's disease. The present work …

[HTML][HTML] A concise review of the recent structural explorations of chromones as MAO-B inhibitors: Update from 2017 to 2023

RS Ipe, S Kumar, F Benny, J Jayan, A Manoharan… - Pharmaceuticals, 2023 - mdpi.com
Monoamine oxidases (MAOs) are a family of flavin adenine dinucleotide-dependent
enzymes that catalyze the oxidative deamination of a wide range of endogenous and …

One-Pot Synthesis of Chromone-2-carboxylate Scaffold: An Important Pharmacophore with Diverse Biological Properties

S Tummanapalli, SK Punna, KC Gulipalli… - The Journal of …, 2023 - ACS Publications
Chromone-2-carboxylate scaffold is growing as an important pharmacophore in medicinal
chemistry with diverse biological properties. We have developed a facile one-pot …

The Suzuki–Miyaura Cross-Coupling–Claisen Rearrangement–Cross-Metathesis Approach to Prenylated Isoflavones

G Kwesiga, J Greese, A Kelling… - The Journal of …, 2023 - ACS Publications
Isoflavones were synthesized via Suzuki–Miyaura coupling of 3-iodochromones and para-
methoxybenzene-and para-phenolboronic acid. In our hands, conditions commonly used for …

[HTML][HTML] Design, synthesis, and biological evaluation of morpholinopyrimidine derivatives as anti-inflammatory agents

S Fatima, A Zaki, H Madhav, BS Khatoon, A Rahman… - RSC …, 2023 - pubs.rsc.org
Here, we outline the synthesis of a few 2-methoxy-6-((4-(6-morpholinopyrimidin-4-yl)
piperazin-1-yl)(phenyl) methyl) phenol derivatives and assess their anti-inflammatory activity …

Isocyanide-based multicomponent reactions for the synthesis of benzopyran derivatives with biological scaffolds

MT Nazeri, T Nasiriani, S Torabi… - Organic & Biomolecular …, 2024 - pubs.rsc.org
Benzopyrans (BZPs) are one of the most privileged and influential small O-heterocycles that
form the core of many natural compounds, commercial drugs, biological compositions …

Substitution controlled aryne insertion: synthesis of diarylmethane/chromones

JR Dhanaji, P Samatha, S Raju, PS Mainkar… - Chemical …, 2023 - pubs.rsc.org
Aryne insertion reaction with 2-aroyl malonates/cyanoesters lead to the formation of
diarylmethane or chromones depending on the substitution on the aryne ring. The presence …

[HTML][HTML] Synthesis and antibacterial activity of pyrano [3, 2-g] chromene-4, 6-dione derivatives and their molecular docking and DFT calculation studies

J Mullaivendhan, A Ahamed, G Raman… - Results in …, 2023 - Elsevier
Pyran-4-one and chromenone are well known bioactive compounds, particularly
antimicrobial activity. Present study investigation antibacterial activity of pyranone connected …