Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Fabio Sparatore"'
Autor:
Fabio Sparatore, Anna Sparatore
Publikováno v:
Molecules, Vol 29, Iss 1, p 132 (2023)
By reducing the 2-nitrophenylhydrazone of cyclohexanone with sodium dithionite, an unexpected yellow compound was obtained instead of the corresponding colorless amino derivative. Many years later, the structure of this compound, namely, cyclohexane-
Externí odkaz:
https://doaj.org/article/e6820b0e4f944018891059169188d5eb
Autor:
Bruno Tasso, Laura Beatrice Mattioli, Michele Tonelli, Vito Boido, Alberto Chiarini, Fabio Sparatore, Roberta Budriesi
Publikováno v:
Molecules, Vol 28, Iss 19, p 6916 (2023)
Fourteen quinolizidine derivatives, structurally related to the alkaloids lupinine and cytisine and previously studied for other pharmacological purposes, were presently tested for antiarrhythmic, and other cardiovascular effects on isolated guinea p
Externí odkaz:
https://doaj.org/article/829011b682184e4f9a877675e7ef0c61
Autor:
Michele Tonelli, Elena Gabriele, Francesca Piazza, Nicoletta Basilico, Silvia Parapini, Bruno Tasso, Roberta Loddo, Fabio Sparatore, Anna Sparatore
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 210-226 (2018)
Two sets of benzimidazole derivatives were synthesised and tested in vitro for activity against promastigotes of Leishmania tropica and L. infantum. Most of the tested compounds resulted active against both Leishmania species, with IC50 values in the
Externí odkaz:
https://doaj.org/article/ae3caed1eed44284ab707d5b717ae1ac
Autor:
Vito Boido, Marcella Ercoli, Michele Tonelli, Federica Novelli, Bruno Tasso, Fabio Sparatore, Elena Cichero, Paola Fossa, Paola Dorigo, Guglielmina Froldi
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 588-599 (2017)
Positive inotropic agents are fundamental in the treatment of heart failure; however, their arrhythmogenic liability and the increased myocardial oxygen demand strongly limit their therapeutic utility. Pursuing our study on cardiovascular activities
Externí odkaz:
https://doaj.org/article/8a8b34dde1414dbf8e141cd391ec21a0
Publikováno v:
ARKIVOC, Vol 2004, Iss 5, Pp 364-374 (2004)
Externí odkaz:
https://doaj.org/article/7f93c998a1444e779941839487966547
Autor:
Michele Tonelli, Marco Catto, Raimon Sabaté, Valeria Francesconi, Erik Laurini, Sabrina Pricl, Leonardo Pisani, Daniela Valeria Miniero, Grazia Maria Liuzzi, Elena Gatta, Annalisa Relini, Rosalina Gavín, Jose Antonio Del Rio, Fabio Sparatore, Angelo Carotti
Publikováno v:
European Journal of Medicinal Chemistry. 250:115169
A set of twenty-five thioxanthene-9-one and xanthene-9-one derivatives, that were previously shown to inhibit cholinesterases (ChEs) and amyloid β (Aβ40) aggregation, were evaluated for the inhibition of tau protein aggregation. All compounds exhib
Autor:
Alexey Koval a, 1, Ivan Bassanini b, k, Jiabin Xu a, c, Michele Tonelli d, Vito Boido d, Fabio Sparatore d, Frederic Amant e, f, g, Daniela Annibali e, Eleonora Leucci h, i, Anna Sparatore b, 2, Vladimir L. Katanaev a, j
Publikováno v:
European journal of medicinal chemistry, 222:113562. Elsevier Masson SAS
European Journal of Medicinal Chemistry, Vol. 222 (2021) P. 113562
European journal of medicinal chemistry 222 (2021). doi:10.1016/j.ejmech.2021.113562
info:cnr-pdr/source/autori:Alexey Koval a, 1, Ivan Bassanini b, k, 1, Jiabin Xu a, c, 1, Michele Tonelli d, Vito Boido d,Fabio Sparatore d, Frederic Amant e, f, g, Daniela Annibali e, Eleonora Leucci h, i, Anna Sparatore b, 2, **, Vladimir L. Katanaev a, j, 2,/titolo:Optimization of the clofazimine structure leads to a highly water-soluble C3-aminopyridinyl riminophenazine endowed with improved anti-Wnt and anti-cancer activity in vitro and in vivo/doi:10.1016%2Fj.ejmech.2021.113562/rivista:European journal of medicinal chemistry/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:222
European Journal of Medicinal Chemistry, Vol. 222 (2021) P. 113562
European journal of medicinal chemistry 222 (2021). doi:10.1016/j.ejmech.2021.113562
info:cnr-pdr/source/autori:Alexey Koval a, 1, Ivan Bassanini b, k, 1, Jiabin Xu a, c, 1, Michele Tonelli d, Vito Boido d,Fabio Sparatore d, Frederic Amant e, f, g, Daniela Annibali e, Eleonora Leucci h, i, Anna Sparatore b, 2, **, Vladimir L. Katanaev a, j, 2,/titolo:Optimization of the clofazimine structure leads to a highly water-soluble C3-aminopyridinyl riminophenazine endowed with improved anti-Wnt and anti-cancer activity in vitro and in vivo/doi:10.1016%2Fj.ejmech.2021.113562/rivista:European journal of medicinal chemistry/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:222
Triple-negative breast cancer (TNBC) is a cancer subtype critically dependent upon excessive activation of Wnt pathway. The anti-mycobacterial drug clofazimine is an efficient inhibitor of canonical Wnt signaling in TNBC, reducing tumor cell prolifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4856f758b929c336decae0b21e42f517
https://pure.amc.nl/en/publications/optimization-of-the-clofazimine-structure-leads-to-a-highly-watersoluble-c3aminopyridinyl-riminophenazine-endowed-with-improved-antiwnt-and-anticancer-activity-in-vitro-and-in-vivo(714f018b-0ab1-45e4-a0ee-40f009600f61).html
https://pure.amc.nl/en/publications/optimization-of-the-clofazimine-structure-leads-to-a-highly-watersoluble-c3aminopyridinyl-riminophenazine-endowed-with-improved-antiwnt-and-anticancer-activity-in-vitro-and-in-vivo(714f018b-0ab1-45e4-a0ee-40f009600f61).html
Autor:
Nicoletta Basilico, Francesca Piazza, Roberta Loddo, Elena Gabriele, Fabio Sparatore, Michele Tonelli, Silvia Parapini, Anna Sparatore, Bruno Tasso
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 33, Iss 1, Pp 210-226 (2018)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
Two sets of benzimidazole derivatives were synthesised and tested in vitro for activity against promastigotes of Leishmania tropica and L. infantum. Most of the tested compounds resulted active against both Leishmania species, with IC50 values in the
Autor:
Paola Dorigo, Michele Tonelli, Vito Boido, Marcella Ercoli, Fabio Sparatore, Bruno Tasso, Guglielmina Froldi, Paola Fossa, Federica Novelli, Elena Cichero
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 588-599 (2017)
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 588-599 (2017)
Positive inotropic agents are fundamental in the treatment of heart failure; however, their arrhythmogenic liability and the increased myocardial oxygen demand strongly limit their therapeutic utility. Pursuing our study on cardiovascular activities
Autor:
Roberta Loddo, Ilenia Delogu, Vito Boido, Michele Tonelli, Gabriele Giliberti, Federica Novelli, Paolo La Colla, Anna Sparatore, Gabriella Collu, Bruno Tasso, Fabio Sparatore
Publikováno v:
Bioorganic & Medicinal Chemistry. 23:7024-7034
A library of 64 benzotriazole derivatives (17 of which were [4-(benzotriazol-2-yl)phenoxy]alkanoic acids) were screened for antiviral activity against a panel of twelve DNA and RNA viruses. Twenty-six compounds (12 of which were [4-(benzotriazol-2-yl