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Design, synthesis, and evaluation of multitarget-directed ligands against Alzheimer’s disease based on the fusion of donepezil and curcumin
- Source :
- Bioorganic & Medicinal Chemistry. 25:2946-2955
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- By fusing donepezil and curcumin, a novel series of compounds were obtained as multitarget-directed ligands against Alzheimer's disease. Among them, compound 11b displayed potent acetylcholinesterase (AChE) inhibition (IC50=187nM) and the highest BuChE/AChE selectivity (66.3). Compound 11b also inhibited 45.3% Aβ1-42 self-aggregation at 20μM and displayed remarkable antioxidant effects. The metal-chelating property of compound 11b was elucidated by determining the 1:1 stoichiometry for the 11b-Cu(II) complex. The excellent blood-brain barrier permeability of 11b also indicated the potential for the compound to penetrate the central nervous system.
- Subjects :
- 0301 basic medicine
Curcumin
Antioxidant
Swine
Aché
Stereochemistry
medicine.medical_treatment
Clinical Biochemistry
Central nervous system
Pharmaceutical Science
Pharmacology
Ligands
Biochemistry
Protein Aggregates
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Piperidines
Alzheimer Disease
Drug Discovery
medicine
Animals
Humans
Donepezil
Molecular Targeted Therapy
Molecular Biology
IC50
Amyloid beta-Peptides
Chemistry
Organic Chemistry
Acetylcholinesterase
Peptide Fragments
language.human_language
Molecular Docking Simulation
030104 developmental biology
medicine.anatomical_structure
Blood-Brain Barrier
Drug Design
Electrophorus
Indans
language
Molecular Medicine
Cholinesterase Inhibitors
Selectivity
030217 neurology & neurosurgery
medicine.drug
Subjects
Details
- ISSN :
- 09680896
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....950cf107bc5e698c239161e88060cea7