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Novel cinnamamide-dibenzylamine hybrids: Potent neurogenic agents with antioxidant, cholinergic, and neuroprotective properties as innovative drugs for Alzheimer's disease
- Source :
- European Journal of Medicinal Chemistry. 139:68-83
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- By using fragments endowed with interesting and complementary properties for the treatment of Alzheimer's disease (AD), a novel series of cinnamamide-dibenzylamine hybrids have been designed, synthesized, and evaluated biologically. In vitro assay indicated that most of the target compounds exhibited a significant ability to inhibit ChEs, strong potency inhibitory of self-induced β -amyloid (A β ) aggregation and to act as potential antioxidants and biometal chelators. A Lineweaver-Burk plot and molecular modeling study showed that compound 7f targeted both the CAS and PAS of AChE. In addition, compound 7f could chelate metal ions, reduce PC12 cells death induced by oxidative stress and penetrate the blood–brain barrier (BBB). Overall, all of these outstanding in vitro results in combination with promising in vivo outcomes highlighted derivative 7f as the lead structure worthy of further investigation.
- Subjects :
- 0301 basic medicine
Benzylamines
Antioxidant
Amyloid
Aché
medicine.medical_treatment
Cholinergic Agents
Pharmacology
medicine.disease_cause
PC12 Cells
01 natural sciences
Neuroprotection
Antioxidants
Structure-Activity Relationship
03 medical and health sciences
Alzheimer Disease
Blood-Retinal Barrier
Drug Discovery
medicine
Animals
Humans
Chelation
Cholinesterase
Cell Death
Dose-Response Relationship, Drug
Molecular Structure
biology
010405 organic chemistry
Chemistry
Organic Chemistry
General Medicine
language.human_language
Rats
0104 chemical sciences
Oxidative Stress
Neuroprotective Agents
030104 developmental biology
Cinnamates
Butyrylcholinesterase
Acetylcholinesterase
biology.protein
language
Cholinergic
Cholinesterase Inhibitors
Oxidative stress
Subjects
Details
- ISSN :
- 02235234
- Volume :
- 139
- Database :
- OpenAIRE
- Journal :
- European Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....ba9fa8f1aa0f82c34956f960bcd26a74
- Full Text :
- https://doi.org/10.1016/j.ejmech.2017.07.077