Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Donatella, Bagetta"'
Autor:
Paolo Guglielmi, Daniela Secci, Anél Petzer, Donatella Bagetta, Paola Chimenti, Giulia Rotondi, Claudio Ferrante, Lucia Recinella, Sheila Leone, Stefano Alcaro, Gokhan Zengin, Jacobus P. Petzer, Francesco Ortuso, Simone Carradori
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 1511-1525 (2019)
A series of benzo[b]thiophen-3-ols were synthesised and investigated as potential human monoamine oxidase (hMAO) inhibitors in vitro as well as ex vivo in rat cortex synaptosomes by means of evaluation of 3,4-dihydroxyphenylacetic acid/dopamine (DOPA
Externí odkaz:
https://doaj.org/article/7280406604314cb88e2b4f9137207ce4
Autor:
Daniela Secci, Simone Carradori, Anél Petzer, Paolo Guglielmi, Melissa D’Ascenzio, Paola Chimenti, Donatella Bagetta, Stefano Alcaro, Gokhan Zengin, Jacobus P. Petzer, Francesco Ortuso
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 597-612 (2019)
A new series of 4-(3-nitrophenyl)thiazol-2-ylhydrazone derivatives were designed, synthesised, and evaluated to assess their inhibitory effect on the human monoamine oxidase (hMAO) A and B isoforms. Different (un)substituted (hetero)aromatic substitu
Externí odkaz:
https://doaj.org/article/5a66b83f76a94eb594765e493cf83d5e
Autor:
Francesco Ortuso, Donatella Bagetta, Annalisa Maruca, Carmine Talarico, Maria L. Bolognesi, Norbert Haider, Fernanda Borges, Sharon Bryant, Thierry Langer, Hanoch Senderowitz, Stefano Alcaro
Publikováno v:
Frontiers in Chemistry, Vol 6 (2018)
For every lead compound developed in medicinal chemistry research, numerous other inactive or less active candidates are synthetized/isolated and tested. The majority of these compounds will not be selected for further development due to a sub-optima
Externí odkaz:
https://doaj.org/article/48ebb914cdde44b993c7c7060ad90c09
Autor:
Joana Reis, Carlos Fernandes, Hoda Salem, Marta Maia, Cláudia Tomé, Sofia Benfeito, José Teixeira, Paulo J. Oliveira, Eugenio Uriarte, Francesco Ortuso, Stefano Alcaro, Donatella Bagetta, Fernando Cagide, Fernanda Borges
Publikováno v:
European journal of medicinal chemistry. 239
The absence of disease modifying drugs in Parkinson's disease therapy urges for new chemical entities acting on relevant PD-associated biological targets. As a result, developing selective and reversible inhibitors targeting MAO-B is still a desirabl
Autor:
Amina Moutayakine, Carolina Marques, Óscar López, Donatella Bagetta, Luisa Leitzbach, Stefanie Hagenow, Elisabete P. Carreiro, Holger Stark, Stefano Alcaro, José G. Fernández-Bolaños, Anthony J. Burke
Publikováno v:
Bioorganicmedicinal chemistry. 68
The chromane ring system is widely distributed in nature and has proven to be a highly potent pharmacophore in medicinal chemistry, which includes the area of Alzheimer's and Parkinson's diseases. We report on the development of a gem-dimethylchroman
Autor:
Gokhan Zengin, Melissa D'Ascenzio, Stefano Alcaro, Anél Petzer, Paolo Guglielmi, Daniela Secci, Simone Carradori, Francesco Ortuso, Jacobus P. Petzer, Paola Chimenti, Donatella Bagetta
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 597-612 (2019)
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 597-612 (2019)
WOS: 000457961800001
PubMed: 30727777
A new series of 4-(3-nitrophenyl)thiazol-2-ylhydrazone derivatives were designed, synthesised, and evaluated to assess their inhibitory effect on the human monoamine oxidase (hMAO) A and B isoforms. Dif
PubMed: 30727777
A new series of 4-(3-nitrophenyl)thiazol-2-ylhydrazone derivatives were designed, synthesised, and evaluated to assess their inhibitory effect on the human monoamine oxidase (hMAO) A and B isoforms. Dif
Autor:
Annalisa Maruca, Francesca Alessandra Ambrosio, Antonio Lupia, Isabella Romeo, Roberta Rocca, Federica Moraca, Carmine Talarico, Donatella Bagetta, Raffaella Catalano, Giosuè Costa, Anna Artese, Stefano Alcaro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f18f061b3a2fb4cb8f0ea007af879d1
https://doi.org/10.1515/9783110579352-013
https://doi.org/10.1515/9783110579352-013
Autor:
Antonio Lupia, Federica Moraca, Donatella Bagetta, Annalisa Maruca, Francesca Alessandra Ambrosio, Roberta Rocca, Raffaella Catalano, Isabella Romeo, Carmine Talarico, Francesco Ortuso, Anna Artese, Stefano Alcaro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::642c5dcdbc548b377bdb358d7cccbe52
https://doi.org/10.1515/9783110579352-014
https://doi.org/10.1515/9783110579352-014
Autor:
Donatella Bagetta, Maria Laura Bolognesi, Sabrina Petralla, Michael Decker, Barbara Monti, Stefano Alcaro, Elisabete P. Carreiro, José G. Fernández-Bolaños, Matthias Hoffmann, Anthony J. Burke, Carolina S. Marques, Óscar López, Manuela Bartolini
Our goal was the evaluation of a series of N-1,2,3-triazole-isatin derivatives for multi-target activity which included cholinesterase (ChE) inhibition and β-amyloid (Aβ) peptide anti-aggregation. The compounds have shown considerable promise as bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4852b3e4794e934182ae50929d021a34
http://hdl.handle.net/11585/786562
http://hdl.handle.net/11585/786562
Autor:
Tiago H. Silva, Francesco Ortuso, Eugenio Uriarte, Maria João Matos, Joana Reis, Stefano Alcaro, André Fonseca, Fernanda Borges, Donatella Bagetta
Publikováno v:
Journal of Medicinal Chemistry. 60:7206-7212
Because of the lack of significant disease-modifying drugs for neurodegenerative disorders, a pressing need for new chemical entities endowed with IMAO-B still exists. Within this framework, and for the first time, a study was performed to compare co