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Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase
Thirteen known (1–12 and 16) and three previously undescribed Amaryllidaceae alkaloids of belladine structural type, named carltonine A-C (13–15), were isolated from bulbs of Narcissus pseudonarcissus cv. Carlton (Amaryllidaceae) by standard chromatographic methods. Compounds isolated in sufficient...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277649/ https://www.ncbi.nlm.nih.gov/pubmed/32455879 http://dx.doi.org/10.3390/biom10050800 |
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author | Al Mamun, Abdullah Maříková, Jana Hulcová, Daniela Janoušek, Jiří Šafratová, Marcela Nováková, Lucie Kučera, Tomáš Hrabinová, Martina Kuneš, Jiří Korábečný, Jan Cahlíková, Lucie |
author_facet | Al Mamun, Abdullah Maříková, Jana Hulcová, Daniela Janoušek, Jiří Šafratová, Marcela Nováková, Lucie Kučera, Tomáš Hrabinová, Martina Kuneš, Jiří Korábečný, Jan Cahlíková, Lucie |
author_sort | Al Mamun, Abdullah |
collection | PubMed |
description | Thirteen known (1–12 and 16) and three previously undescribed Amaryllidaceae alkaloids of belladine structural type, named carltonine A-C (13–15), 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; E.C. 3.1.1.7), butyrylcholinesterase (BuChE; E.C. 3.1.1.8) and prolyl oligopeptidase (POP; 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 IC(50) values of 913 ± 20 nM and 31 ± 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. |
format | Online Article Text |
id | pubmed-7277649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72776492020-06-12 Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase Al Mamun, Abdullah Maříková, Jana Hulcová, Daniela Janoušek, Jiří Šafratová, Marcela Nováková, Lucie Kučera, Tomáš Hrabinová, Martina Kuneš, Jiří Korábečný, Jan Cahlíková, Lucie Biomolecules Article Thirteen known (1–12 and 16) and three previously undescribed Amaryllidaceae alkaloids of belladine structural type, named carltonine A-C (13–15), 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; E.C. 3.1.1.7), butyrylcholinesterase (BuChE; E.C. 3.1.1.8) and prolyl oligopeptidase (POP; 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 IC(50) values of 913 ± 20 nM and 31 ± 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. MDPI 2020-05-22 /pmc/articles/PMC7277649/ /pubmed/32455879 http://dx.doi.org/10.3390/biom10050800 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Al Mamun, Abdullah Maříková, Jana Hulcová, Daniela Janoušek, Jiří Šafratová, Marcela Nováková, Lucie Kučera, Tomáš Hrabinová, Martina Kuneš, Jiří Korábečný, Jan Cahlíková, Lucie Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title | Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title_full | Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title_fullStr | Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title_full_unstemmed | Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title_short | Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase |
title_sort | amaryllidaceae alkaloids of belladine-type from narcissus pseudonarcissus cv. carlton as new selective inhibitors of butyrylcholinesterase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277649/ https://www.ncbi.nlm.nih.gov/pubmed/32455879 http://dx.doi.org/10.3390/biom10050800 |
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