Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Paola Turini"'
Autor:
Antonello Mai, Marino Artico, Sergio Valente, Ilaria Cerbara, Olivia Befani, Paola Turini Laura Dalla Vedova, Enzo Agostinelli
Publikováno v:
ARKIVOC, Vol 2004, Iss 5, Pp 32-43 (2004)
Externí odkaz:
https://doaj.org/article/b30adb18e3e7444bbb053a2c2bff0ee1
Autor:
Beatrice Campi, Giovanni Taccetti, Alessandro Saba, Giancarlo la Marca, G. Mergni, Paola Turini, Paolo Scardina, Massimo Pifferi, Maria Di Cicco, Antonella Marvelli, Riccardo Zucchi, Aldo Paolicchi
Publikováno v:
Analytical and Bioanalytical Chemistry
The current guidelines for sweat chloride analysis identify the procedures for sweat collection, but not for chloride assay, which is usually performed by methods originally not aiming at the low concentrations of chloride found in sweat. To overcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a7710194a1d141ba69b9d77420564f
https://doi.org/10.1007/s00216-020-02821-3
https://doi.org/10.1007/s00216-020-02821-3
It is well recognized that variation in the geographical distribution of prevalence of multiple sclerosis (MS) exists: increasing the latitude its prevalence increases as well, but the underlying causes of such dissimilarity still remained elusive as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4db1dffdf28c42a663f1d4c274b3278d
http://hdl.handle.net/11573/1337444
http://hdl.handle.net/11573/1337444
Autor:
Paola Turini, Francesco Ortuso, Olivia Befani, Adriana Bolasco, Daniela Secci, Franco Chimenti, Paola Chimenti, Fedele Manna, Arianna Granese, Stefano Alcaro
Publikováno v:
Chemical Biology Drug Design. 67:206-214
This report describes novel pyrazoline derivatives investigated for their ability to selectively inhibit the activity of the A and B isoforms of monoamine oxidase. These new synthetic compounds proved to be reversible, potent, and selective inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d814ea61bae593953183e96f5cb6129c
https://doi.org/10.1111/j.1747-0285.2006.00367.x
https://doi.org/10.1111/j.1747-0285.2006.00367.x
Autor:
Francesco Ortuso, Francesco La Torre, Roberto Cirilli, Simona Distinto, Maria Cristina Cardia, Daniela Secci, Stefano Alcaro, Arianna Granese, Elias Maccioni, Franco Chimenti, Adriana Bolasco, Olivia Befani, Paola Chimenti, Paola Turini
Publikováno v:
Journal of Medicinal Chemistry. 48:7113-7122
A novel series of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazole derivatives have been synthesized and investigated for the ability to inhibit selectively the activity of the A and B isoforms of monoamine oxidase (MAO). All the synthesized comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f95c6b4b9ef6c4f191840571ebe56c
https://doi.org/10.1021/jm040903t
https://doi.org/10.1021/jm040903t
Autor:
Paola Turini, Alessandra Roux, Marino Artico, Paola Palmegiani, Tiziana Meninno, Francesco La Torre, Roberto Cirilli, Enzo Agostinelli, Rosella Ferretti, Roberta Costi, Olivia Befani, Bruno Gallinella, Roberto Di Santo
Publikováno v:
Journal of Medicinal Chemistry. 48:4220-4223
Pyrrolylethanoneamines 1-12, 18-23 and related amino alcohols 13-15, 24-27 were synthesized and tested against monoamine oxidases A and B (MAO-A and MAO-B) enzymes. In general, aminoketones 1-12, 18-23 were found to be potent and selective MAO-A inhi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b255f1c83cdaccf780504af7b3fc863
https://doi.org/10.1021/jm050172c
https://doi.org/10.1021/jm050172c
Autor:
Gianluca Sbardella, Marco Artico, Paola Turini, Enzo Agostinelli, Olivia Befani, L. Dalla Vedova, Antonello Mai, Sergio Valente
Publikováno v:
Scopus-Elsevier
A novel series of 5-substituted-3-(1H-pyrrol-2-yl)-2-oxazolidinones 2a-s has been described as pyrrole analogues of toloxatone and befloxatone, two phenyl-oxazolidinones active as anti-MAO agents and used in antidepressant therapy. Tested against MAO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82066a1178efc65f320048b6bb01eb79
https://doi.org/10.2174/1573406053175247
https://doi.org/10.2174/1573406053175247
Autor:
Paola Turini Laura Dalla Vedova, Antonello Mai, Sergio Valente, Marino Artico, Olivia Befani, Enzo Agostinelli, Ilaria Cerbara
Publikováno v:
ARKIVOC, Vol 2004, Iss 5, Pp 32-43 (2004)
R)-5-Acyloxymethyland (S)-5-acylaminomethyl-3-(1H-pyrrol-1-yl)-2-oxazolidinones 2a-s were synthesized as pyrrole analogues of toloxatone (Humoryl), an anti-MAO agent used in clinical therapy because of its antidepressant properties. Their ability to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1798097dfc3b635ec365ca5582a23ef6
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0005.504
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0005.504
Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives
Autor:
Bruna Bizzarri, Paola Turini, Stefano Alcaro, Olivia Befani, Andrea Tafi, Fedele Manna, Bruno Mondovi, Daniela Secci, Franco Chimenti, Adriana Bolasco
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 12:3629-3633
A novel series of 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives have been synthesised and investigated for the ability to inhibit selectively monoamine oxidases, swine kidney oxidase, and bovine serum amine oxidase. The newly synthesise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c4583dac355130cb319544d6f5e519
https://doi.org/10.1016/s0960-894x(02)00699-6
https://doi.org/10.1016/s0960-894x(02)00699-6
Autor:
Bruna Bizzarri, Franco Chimenti, Paola Turini, Paola Pietrangeli, Adriana Bolasco, Olivia Befani, Fedele Manna, Bruno Mondovi
Publikováno v:
Scopus-Elsevier
A new series of 1,3,5-triphenyl-4,5-dihydro-(1H)-pyrazole derivatives was synthesized to ascertain the contribution of substituted phenyl rings present on the 4,5-dihydro-(1H)-pyrazole nucleus to the monoamine oxidases inhibition and bovine serum ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6926b697e07830f75810fc0c9aec6c6
https://doi.org/10.3109/14756369809028341
https://doi.org/10.3109/14756369809028341