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Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase
- Source :
- Biomolecules, Vol 10, Iss 800, p 800 (2020), Biomolecules, Volume 10, Issue 5
- Publication Year :
- 2020
- Publisher :
- MDPI AG, 2020.
-
Abstract
- Thirteen known (1&ndash<br />12 and 16) and three previously undescribed Amaryllidaceae alkaloids of belladine structural type, named carltonine A-C (13&ndash<br />15), were isolated from bulbs of Narcissus pseudonarcissus cv. Carlton (Amaryllidaceae) by standard chromatographic methods. Compounds isolated in sufficient amounts, and not tested previously, were evaluated for their in vitro acetylcholinesterase (AChE<br />E.C. 3.1.1.7), butyrylcholinesterase (BuChE<br />E.C. 3.1.1.8) and prolyl oligopeptidase (POP<br />E.C. 3.4.21.26) inhibition activities. Significant human BuChE (hBUChE) inhibitory activity was demonstrated by newly described alkaloids carltonine A (13) and carltonine B (14) with IC50 values of 913 &plusmn<br />20 nM and 31 &plusmn<br />1 nM, respectively. Both compounds displayed a selective inhibition pattern for hBuChE with an outstanding selectivity profile over AChE inhibition, higher than 100. The in vitro data were further supported by in silico studies of the active alkaloids 13 and 14 in the active site of hBuChE.
- Subjects :
- Aché
Stereochemistry
Narcissus pseudonarcissus cv. Carlton
lcsh:QR1-502
Oligopeptidase
alkaloids
01 natural sciences
Biochemistry
lcsh:Microbiology
03 medical and health sciences
chemistry.chemical_compound
Amaryllidaceae Alkaloids
Molecular Biology
Butyrylcholinesterase
030304 developmental biology
0303 health sciences
biology
010405 organic chemistry
Amaryllidaceae
Active site
docking studies
biology.organism_classification
Acetylcholinesterase
language.human_language
In vitro
0104 chemical sciences
carltonine A–C
chemistry
butyrylcholinesterase
biology.protein
language
Alzheimer’s disease
Subjects
Details
- Language :
- English
- Volume :
- 10
- Issue :
- 800
- Database :
- OpenAIRE
- Journal :
- Biomolecules
- Accession number :
- edsair.doi.dedup.....8db1e763ad623254f7edf6d1f9d40f44