Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Magne O. Sydnes"'
Autor:
Bodil Bjørndal, Siri Lunde Tungland, Pavol Bohov, Magne O. Sydnes, Simon N. Dankel, Lise Madsen, Rolf K Berge
Publikováno v:
Liver Research, Vol 8, Iss 3, Pp 152-164 (2024)
Background and objective: Metabolic associated fatty liver disease (MAFLD) is associated with abnormal lipid metabolism. Mitochondrial dysfunction is considered an important factor in the onset of MAFLD, whereas altered fatty acid composition has bee
Externí odkaz:
https://doaj.org/article/f184559c38b14a08a85a87ff27b29649
Autor:
Omar F. Luna, Yomkippur V. Perez, Daniele P. Ferrari, Sana S. Sayedipour, Miriam Royo, Gerardo A. Acosta, Luis J. Cruz, Frauke Alves, Erik Agner, Magne O. Sydnes, Fernando Albericio
Publikováno v:
ACS Omega, Vol 9, Iss 32, Pp 34544-34554 (2024)
Externí odkaz:
https://doaj.org/article/a9c3cf5149c04adc9dd0a7f27bf09808
Autor:
I. Caroline Vaaland, Óscar López, Adrián Puerta, Miguel X. Fernandes, José M. Padrón, José G. Fernández-Bolaños, Magne O. Sydnes, Emil Lindbäck
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 38, Iss 1, Pp 349-360 (2023)
The copper-catalysed azide-alkyne cycloaddition was applied to prepare three enantiomeric pairs of heterodimers containing a tacrine residue and a 1,4-dideoxy-1,4-imino-D-arabinitol (DAB) or 1,4-dideoxy-1,4-imino-L-arabinitol (LAB) moiety held togeth
Externí odkaz:
https://doaj.org/article/d1237b9cbbfb410ca4a715968aec2873
Autor:
Tereza Cristina Santos Evangelista, Óscar López, Adrián Puerta, Miguel X. Fernandes, Sabrina Baptista Ferreira, José M. Padrón, José G. Fernández-Bolaños, Magne O. Sydnes, Emil Lindbäck
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 37, Iss 1, Pp 2395-2402 (2022)
The synthesis of four heterodimers in which the copper(I)-catalysed azide-alkyne cycloaddition was employed to connect a 1-deoxynojirimycin moiety with a benzotriazole scaffold is reported. The heterodimers were investigated as inhibitors against ace
Externí odkaz:
https://doaj.org/article/ab088dcc1fde417ebcc32bdfc2fb0a36
Publikováno v:
Heliyon, Vol 8, Iss 12, Pp e12625- (2022)
The presence and levels of fifteen chemicals of emerging concerns, including five perfluorinated compounds (PFCs), two industrial chemicals, seven pharmaceuticals and one personal care product, were evaluated in biota, seawater and sediments obtained
Externí odkaz:
https://doaj.org/article/bb9ff95433f243589ec3fe685c93b05f
Autor:
Tereza Cristina Santos Evangelista, Óscar López, Sabrina Baptista Ferreira, José G. Fernández-Bolaños, Magne O. Sydnes, Emil Lindbäck
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 36, Iss 1, Pp 1658-1663 (2021)
The synthesis of four tetra-tacrine clusters where the tacrine binding units are attached to a central scaffold via linkers of variable lengths is described. The multivalent inhibition potencies for the tacrine clusters were investigated for the inhi
Externí odkaz:
https://doaj.org/article/d61cbdc315484d868f3fc5e950cdaea6
Autor:
Marianne B. Haarr, Óscar Lopéz, Ljupcho Pejov, José G. Fernández-Bolaños, Emil Lindbäck, Magne O. Sydnes
Publikováno v:
ACS Omega, Vol 5, Iss 29, Pp 18507-18514 (2020)
Externí odkaz:
https://doaj.org/article/6bb8cee591724f2b85a2d237179958bd
Publikováno v:
ACS Omega, Vol 3, Iss 7, Pp 7344-7349 (2018)
Externí odkaz:
https://doaj.org/article/83dc82b12ceb4c5b897a4c34b2410a8b
Publikováno v:
SynOpen, Vol 01, Iss 01, Pp 0041-0044 (2017)
Abstract Isocryptolepine (1), a potent antimalarial natural product, was prepared in three steps from 3-bromoquinoline and 2-aminophenylboronic acid hydrochloride. The key transformations were a Suzuki–Miyaura cross-coupling reaction followed by a
Externí odkaz:
https://doaj.org/article/64c8452fdcfe43889314df430355d162
Publikováno v:
Heliyon, Vol 5, Iss 5, Pp e01701- (2019)
Externí odkaz:
https://doaj.org/article/4e4818135d1c466eb33d59016cb4277b