Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
Spatial distribution and stability of cholinesterase inhibitory protoberberine alkaloids from Papaver setiferum
ID
Safa, Neda
(
Author
),
ID
Trobec, Tomaž
(
Author
),
ID
Holland, Darren C.
(
Author
),
ID
Slazak, Blazej
(
Author
),
ID
Jacobsson, Erik
(
Author
),
ID
Hawkes, Jeffrey A.
(
Author
),
ID
Frangež, Robert
(
Author
),
ID
Sepčić, Kristina
(
Author
),
ID
Göransson, Ulf
(
Author
),
ID
Moodie, Lindon W. K.
(
Author
),
ID
Robertson, Luke P.
(
Author
)
PDF - Presentation file,
Download
(6,46 MB)
MD5: 9FDC39EC268FD2B0551E73995350AE6A
URL - Source URL, Visit
https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.1c00980
Image galllery
Abstract
During a research program to identify new cholinesterase inhibitors of natural origin, two new 7,8-didehydroprotoberberine alkaloids (1 and 2) and nine known compounds (3−11) were isolated from the capsules of the common ornamental poppy, Papaver setiferum (previously P. pseudo-orientale). Despite their reported instability, the 7,8-didehydroprotoberberines isolated herein appeared relatively stable, particularly as their trifluoroacetic acid salts. The spatial distributions of the isolated alkaloids were also analyzed using desorption electrospray ionization imaging mass spectrometry. The alkaloids were localized predominantly within the walls and vascular bundles of the capsules, with the highest relative abundances occurring in the lower half of the capsules toward the peduncle. The relative abundances of the alkaloids were also compared across plant development stages. Although most alkaloids did not show clear patterns in their concentration across development stages, the concentration of suspected oxidation products clearly spiked upon plant death. Finally, all isolated natural products were screened for inhibitory activities against a panel of cholinesterases, from both human and animal sources. These studies identified several competitive inhibitors of cholinesterases with potency in the low micromolar range (1−4, 6, 7), offering new lead compounds for the development of cholinesterase inhibitory drugs
Language:
English
Keywords:
Cholinesterase Inhibitors
,
Papaver
,
Alkaloids
Typology:
1.01 - Original Scientific Article
Organization:
VF - Veterinary Faculty
BF - Biotechnical Faculty
Publication status:
Published
Publication version:
Version of Record
Publication date:
01.01.2022
Year:
2022
Number of pages:
Str. 215-224
Numbering:
Vol. 85, no. 1
PID:
20.500.12556/RUL-140823
UDC:
577
ISSN on article:
1520-6025
DOI:
10.1021/acs.jnatprod.1c00980
COBISS.SI-ID:
89689603
Publication date in RUL:
19.09.2022
Views:
596
Downloads:
126
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Journal of natural products
Shortened title:
J. nat. products
Publisher:
American Chemical Society and American Society of Pharmacognosy
ISSN:
1520-6025
COBISS.SI-ID:
512806937
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
19.09.2022
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P4-0053
Name:
Endokrini, imunski in encimski odzivi pri zdravih in bolnih živalih
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0207
Name:
Toksini in biomembrane
Funder:
Other - Other funder or multiple funders
Project number:
51852
Name:
Junior Research Grant T.T.
Funder:
Other - Other funder or multiple funders
Project number:
F20-0019
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back