Dual BACE1 and Cholinesterase Inhibitory Effects of Phlorotannins from
ADAM17 Protein
/ antagonists & inhibitors
Alzheimer Disease
/ drug therapy
Amyloid Precursor Protein Secretases
/ antagonists & inhibitors
Aspartic Acid Endopeptidases
/ antagonists & inhibitors
Benzofurans
/ chemistry
Cholinesterase Inhibitors
/ pharmacology
Cholinesterases
/ chemistry
Dioxins
/ chemistry
Molecular Docking Simulation
Seaweed
/ chemistry
Tannins
/ chemistry
Alzheimer′s disease
BACE1
acetylcholinesterase
in silico docking
phlorotannins
Journal
Marine drugs
ISSN: 1660-3397
Titre abrégé: Mar Drugs
Pays: Switzerland
ID NLM: 101213729
Informations de publication
Date de publication:
01 Feb 2019
01 Feb 2019
Historique:
received:
08
01
2019
revised:
24
01
2019
accepted:
28
01
2019
entrez:
6
2
2019
pubmed:
6
2
2019
medline:
27
4
2019
Statut:
epublish
Résumé
Alzheimer's disease (AD) is one of the most common neurodegenerative diseases with a multifactorial nature. β-Secretase (BACE1) and acetylcholinesterase (AChE), which are required for the production of neurotoxic β-amyloid (Aβ) and the promotion of Aβ fibril formation, respectively, are considered as prime therapeutic targets for AD. In our efforts towards the development of potent multi-target, directed agents for AD treatment, major phlorotannins such as eckol, dieckol, and 8,8'-bieckol from
Identifiants
pubmed: 30717208
pii: md17020091
doi: 10.3390/md17020091
pmc: PMC6410325
pii:
doi:
Substances chimiques
Benzofurans
0
Cholinesterase Inhibitors
0
Dioxins
0
Tannins
0
dieckol
0
eckol
88798-74-7
8,8'-bieckol
89445-12-5
Cholinesterases
EC 3.1.1.8
Amyloid Precursor Protein Secretases
EC 3.4.-
Aspartic Acid Endopeptidases
EC 3.4.23.-
BACE1 protein, human
EC 3.4.23.46
ADAM17 Protein
EC 3.4.24.86
ADAM17 protein, human
EC 3.4.24.86
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Dong-A University
ID : None
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