Results 81 to 90 of about 10,504 (228)

Molecular docking‐guided in‐depth investigation of the biological activities and phytochemical and mineral profiles of endemic Phlomis capitata

open access: yesJournal of the Science of Food and Agriculture, Volume 105, Issue 7, Page 3760-3775, May 2025.
Abstract BACKGROUND Phlomis capitata is an endemic species of flowering aromatic and medicinal plant in the family Lamiaceae, native to regions of the Mediterranean and nearby areas. Understanding the chemical compounds present in P. capitata can reveal potential medicinal properties.
Ebubekir İzol
wiley   +1 more source

Synthesis of Benzimidazole–Based Analogs as Anti Alzheimer’s Disease Compounds and Their Molecular Docking Studies

open access: yesMolecules, 2020
We synthesized 10 analogs of benzimidazole-based thiosemicarbazide 1 (a–j) and 13 benzimidazole-based Schiff bases 2 (a–m), and characterized by various spectroscopic techniques and evaluated in vitro for acetylcholinesterase (AchE) and ...
Bushra Adalat   +8 more
doaj   +1 more source

Investigation of Thiazolidine‐2,4‐Dione Derivatives as Acetylcholinesterase Inhibitors: Synthesis, In Vitro Biological Activities and In Silico Studies

open access: yesChemistryOpen, Volume 14, Issue 5, May 2025.
Thiazolidin‐2,4‐dion derivatives were synthesized and evaluated for drug‐likeness, BBB permeability, and ADMET properties. Docking studies revealed that all derivatives (CHT1‐5) had good AChE inhibition, although CHT1 was the most effective and showed strong antioxidant activity in vitro.
Hanane Naeimi   +3 more
wiley   +1 more source

In Vitro, Anti‐Colon Cancer Activity of Green Dumbbell‐Shaped Rhododendron luteum‐Based Carbon Dots

open access: yesChemistryOpen, Volume 14, Issue 5, May 2025.
The anticancer potential of Rhododendron luteum‐based carbon dots was investigated. Environmentally friendly synthesis yielded carbon dots that selectively induced cytotoxicity in HCT116 cells by reducing CD44/24 ratio, causing G2/M phase arrest, and enhancing apoptosis.
Alper Durmaz   +6 more
wiley   +1 more source

Inhibition of Butyrylcholinesterase by Phenothiazine Derivatives

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2002
The inhibition of horse serum butyrylcholinesterase (EC 3.1.1.8) by 10 phenothiazine or thioxanthene derivatives was studied with a purified enzyme. Most compounds were mixed inhibitors, but for some of them an apparent competitive inhibition was observed. The competitive inhibition constants (K) were in the range 0.05 to 5 microM.
Jean Debord   +3 more
openaire   +3 more sources

Novel pyridazinone derivatives as butyrylcholinesterase inhibitors

open access: yesBioorganic Chemistry, 2019
In the current study, forty-four new [3-(2/3/4-methoxyphenyl)-6-oxopyridazin-1(6H)-yl]methyl carbamate derivatives were synthesized and evaluated for their ability to inhibit electric eel acetylcholinesterase (EeAChE) and equine butyrylcholinesterase (eqBuChE) enzymes.
Dundar, Yasemin   +5 more
openaire   +5 more sources

A steady-state kinetic model of butyrylcholinesterase from horse plasma [PDF]

open access: green, 1974
Klas‐Bertil Augustinsson   +2 more
openalex   +1 more source

Rivastigmine: the advantages of dual inhibition of acetylcholinesterase and butyrylcholinesterase and its role in subcortical vascular dementia and Parkinson’s disease dementia

open access: yesClinical Interventions in Aging, 2017
Nagaendran Kandiah,1,2 Ming-Chyi Pai,3,4 Vorapun Senanarong,5 Irene Looi,6,7 Encarnita Ampil,8 Kyung Won Park,9 Ananda Krishna Karanam,10 Stephen Christopher11 1Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, 2Duke-NUS,
Kandiah N   +7 more
doaj  

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