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
N-hydroxy-N-propargylamide derivatives of ferulic acid : inhibitors of cholinesterases and monoamine oxidases
ID
Bautista-Aguilera, Oscar M.
(
Author
),
ID
Alonso, José M.
(
Author
),
ID
Catto, Marco
(
Author
),
ID
Iriepa, Isabel
(
Author
),
ID
Knez, Damijan
(
Author
),
ID
Gobec, Stanislav
(
Author
),
ID
Marco-Contelles, José
(
Author
)
PDF - Presentation file,
Download
(792,16 KB)
MD5: 43DB8F68B71C521F26574F9486E9F3A9
URL - Source URL, Visit
https://www.mdpi.com/1420-3049/27/21/7437
Image galllery
Abstract
Alzheimer’s disease (AD) is a complex disorder characterized by impaired neurotransmission in cholinergic and monoaminergic neurons, which, in combination with the accumulation of misfolded proteins and increased oxidative stress, leads to the typical features of the disease at the biomolecular level. Given the limited therapeutic success of approved drugs, it is imperative to explore rationally supported therapeutic approaches to combat this disease. The search for novel scaffolds that bind to different receptors and inhibit AD disease-related enzymes could lead to new therapeutic solutions. Here, we describe N-hydroxy-N-propargylamide hybrids 1–6, which were designed by combining the structures of Contilisant—a multifunctional anti-AD ligand—and ferulic acid, a natural antioxidant with various other biological activities. Among the synthesized compounds, we identified compound 4 as a micromolar inhibitor of hAChE with a potent radical-scavenging capacity comparable to resveratrol and Trolox. In addition, compound 4 chelated copper(II) ions associated with amyloid β pathology, mitochondrial dysfunction, and oxidative stress. The promising in vitro activity combined with favorable drug-like properties and predicted blood‒brain barrier permeability make compound 4 a multifunctional ligand that merits further studies at the biochemical and cellular levels.
Language:
English
Keywords:
cholinesterases
,
ferulic acid
,
molecular modelling
,
monoamine oxidase
,
radical-scavenger
,
antioxidant
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2022
Number of pages:
18 str.
Numbering:
Vol. 27, iss. 21, art. 7437
PID:
20.500.12556/RUL-142354
UDC:
616.894
ISSN on article:
1420-3049
DOI:
10.3390/molecules27217437
COBISS.SI-ID:
127684867
Publication date in RUL:
02.11.2022
Views:
578
Downloads:
95
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:
Molecules
Shortened title:
Molecules
Publisher:
MDPI
ISSN:
1420-3049
COBISS.SI-ID:
18462981
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.
Secondary language
Language:
Slovenian
Keywords:
holinesteraze
,
ferulna kislina
,
molekularno modeliranje
,
monoaminooksidaza
,
lovilec radikalov
,
antioksidant
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0208-2015
Name:
Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back