Advancements in the development of multi-target directed ligands for the treatment of Alzheimer's disease

N Kumar, V Kumar, P Anand, V Kumar… - Bioorganic & Medicinal …, 2022 - Elsevier
Alzheimer's disease (AD) is a multifactorial irreversible neurological disorder which results
in cognitive impairment, loss of cholinergic neurons in synapses of the basal forebrain and …

[HTML][HTML] Unveiling natural and semisynthetic acylated flavonoids: Chemistry and biological actions in the context of molecular docking

DM El-Kersh, RF Abou El-Ezz, M Fouad, MA Farag - Molecules, 2022 - mdpi.com
Acylated flavonoids are widely distributed natural metabolites in medicinal plants and foods
with several health attributes. A large diversity of chemical structures of acylated flavonoids …

Exploring novel anticancer pyrazole benzenesulfonamides featuring tail approach strategy as carbonic anhydrase inhibitors

RF Ahmed, WR Mahmoud, NM Abdelgawad… - European Journal of …, 2023 - Elsevier
This study aimed to design potent carbonic anhydrase inhibitors (CAIs) based on pyrazole
benzenesulfonamide core. Nine series of substituted pyrazole benzenesulfonamide …

[HTML][HTML] A importância das cumarinas para a química medicinal eo desenvolvimento de compostos bioativos nos últimos anos

DP Franco, TM Pereira, F Vitorio, NF Nadur… - Química …, 2021 - SciELO Brasil
Coumarins are natural products characterized as 2H-chromen-2-one, according to IUPAC
nomenclature, largely distributed in plants, as well as, in species of fungi and bacteria …

Dual-target ligand discovery for Alzheimer's disease: triphenylphosphoranylidene derivatives as inhibitors of acetylcholinesterase and β-amyloid aggregation

M El-Hussieny, MA Abd-El-Maksoud… - Journal of Enzyme …, 2023 - Taylor & Francis
Alzheimer disease (AD) is one of the major neurodegenerative diseases that could not be
prevented or completely cured and may lead to death. Here, we target AChE and β-amyloid …

Synthesis of carbazole based α-aminophosphonate derivatives: design, molecular docking and in vitro cholinesterase activity

S Shaikh, P Dhavan, P Singh, J Uparkar… - Journal of …, 2022 - Taylor & Francis
A series of novel carbazole based α-aminophosphonate derivatives were synthesized under
solvent-free condition, characterized and evaluated for their cholinesterase inhibition …

Design, synthesis and biological evaluation of novel antipyrine based α-aminophosphonates as anti-Alzheimer and anti-inflammatory agent

S Shaikh, P Dhavan, P Singh, J Uparkar… - Journal of …, 2023 - Taylor & Francis
Herein, a series of novel antipyrine based α-aminophosphonates derivatives were
synthesized and characterized. The synthesized derivatives were subjected for in vitro …

Efficient and Sustainable Electrosynthesis of N-Sulfonyl Iminophosphoranes by the Dehydrogenative P–N Coupling Reaction

JC Bieniek, DF Nater, SL Eberwein, D Schollmeyer… - JACS Au, 2024 - ACS Publications
Iminophosphoranes are commonly used reagents in organic synthesis and are, therefore, of
great interest. An efficient and sustainable iodide-mediated electrochemical synthesis of N …

Synthesis, biological evaluation, and molecular dynamics of novel coumarin based phosphorothioates as cholinesterase inhibitors

M El-Hussieny, MF ElMansy, EF Ewies… - Journal of Molecular …, 2023 - Elsevier
Inhibition of acetylcholinesterase has been validated as an effective target for treatment of
Alzheimer's disease by increasing the levels of acetylcholine and improving the …

Farnesyl pyrophosphate synthase inhibitors with antiosteoporosis efficacy in ovariectomized rats: A mixed binding approach beyond bisphosphonates

NF El-Sayed, M El-Hussieny, ST Mansour… - European Journal of …, 2024 - Elsevier
The primary focus of bisphosphonate medications is on targeting human farnesyl
pyrophosphate synthase (hFPPS), an essential regulator of mammalian isoprenoids. Yet …