Synthesis, In Silico and In Vitro Evaluation for Acetylcholinesterase and BACE-1 Inhibitory Activity of Some N-Substituted-4-Phenothiazine-Chalcones

TS Tran, MT Le, TCV Nguyen, TH Tran, TD Tran… - Molecules, 2020 - mdpi.com
Acetylcholinesterase (AChE) and beta-secretase (BACE-1) are two attractive targets in the
discovery of novel substances that could control multiple aspects of Alzheimer's disease …

Efficient synthesis of indole-chalcones based glycohybrids and their anticancer activity

R Tyagi, K Yadav, A Khanna, SK Mishra… - Bioorganic & Medicinal …, 2024 - Elsevier
Indole based glycosides belong to the class of pharmacologically active molecules and
found in diverse natural compounds. Herein, we report synthesis of 1, 2, 3-triazole bridged …

Exploring synthetic and therapeutic prospects of new thiazoline derivatives as aldose reductase (ALR2) inhibitors

MT Shehzad, A Imran, A Hameed, M Al Rashida… - RSC …, 2021 - pubs.rsc.org
Inhibition of aldose reductase (ALR2) by using small heterocyclic compounds provides a
viable approach for the development of new antidiabetic agents. With our ongoing interest …

A new series of thiosemicarbazone‐based anti‐inflammatory agents exerting their action through cyclooxygenase inhibition

MD Altıntop, B Sever, G Akalın Çiftçi… - Archiv der …, 2022 - Wiley Online Library
In an endeavor to identify potent anti‐inflammatory agents, new thiosemicarbazones (TSCs)
incorporated into a diaryl ether framework (2a–2l) were prepared and screened for their in …

Inhibition of Mitogen-Activated Protein Kinases/Nuclear Factor κB–Dependent Inflammation by a Novel Chalcone Protects the Kidney from High Fat Diet–Induced …

Q Fang, L Deng, L Wang, Y Zhang, Q Weng… - Journal of pharmacology …, 2015 - ASPET
The prevalence of obesity has increased dramatically worldwide leading to increases in
obesity-related complications, such as obesity-related glomerulopathy (ORG). Obesity is a …

Design, computational, synthesis, characterization, antimicrobial, MTT and molecular docking assessment of bipyrimidine derivatives possessing indole moiety

M Arshad - Journal of the Iranian Chemical Society, 2020 - Springer
An adequate enhancement in the development of resistance by microbial pathogens against
the available chemotherapeutic agents prompted us to find out some new chemotherapeutic …

Facile synthesis, Spectral investigation, in vitro and in silico studies of Thiophenecarboxamide-α, β-unsaturated ketone hybrids

M Bharathi, S Shreedevi, R Sribalan - Journal of Molecular Structure, 2024 - Elsevier
Thiophenecarboxamide-α, β-unsaturated ketone (TCKs) hybrids were synthesized and
scrupulously characterized by nuclear magnetic resonance spectroscopy (NMR) by the …

Synthesis of hydroxybenzofuranyl-pyrazolyl and hydroxyphenyl-pyrazolyl chalcones and their corresponding pyrazoline derivatives as COX inhibitors, anti …

FAEF Ragab, EI Mohammed, GAA Jaleel… - Chemical and …, 2020 - jstage.jst.go.jp
Five new series of hydroxybenzofuranyl-pyrazolyl chalcones 3a, b, hydroxyphenyl-pyrazolyl
chalcones 6a–c and their corresponding pyrazolylpyrazolines 4a, d, 7a–c and 8a–f have …

Novel indolyl-chalcones target stathmin to induce cancer cell death

B Wegiel, Y Wang, M Li, F Jernigan, L Sun - Cell cycle, 2016 - Taylor & Francis
Efficacy of current therapies for advanced and metastatic cancers remains a challenge in
clinical practice. We investigated the anti-cancer potency of 3 novel indoly-chalcones (CITs) …

Trifluoroacetylation of indole-chalcones derived from the 2-amino-3-(arylethynyl)-5-bromo-iodochalcones

MJ Mphahlele, MM Maluleka - Journal of Fluorine Chemistry, 2016 - Elsevier
The present work describes a novel approach for the annulation of an indole moiety onto the
1, 3-diaryl-2-propen-1-one scaffold followed by trifluoroacetylation of the resultant indole …