Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Federica Ravazzini"'
Autor:
Giulia Puia, Federica Ravazzini
Publikováno v:
Pharmacological reports : PR. 72(6)
Thyroid hormones (THs) are crucial for maturation and functioning of mammalian CNS. THs “classical” signaling involves nuclear receptors binding but also their non genomic actions, as rapid modulators of cell activity, are widely recognized. Sinc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7134e465b74b3f3385232322535edd35
https://pubmed.ncbi.nlm.nih.gov/33085069
https://pubmed.ncbi.nlm.nih.gov/33085069
Autor:
Giulia Puia, Brandon M. Brown, Piotr Draczkowski, Ana Belén Elgoyhen, Dominik Feuerbach, Juan Carlos Boffi, Federica Ravazzini, Hugo R. Arias, Katarzyna M. Targowska-Duda, Krzysztof Jozwiak, Dirk Montag, Agnieszka A. Kaczor
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 76:19-30
tThe activity of positive allosteric modulators (PAMs) of 7 nicotinic acetylcholine receptors (AChRs),including 3-furan-2-yl-N-p-tolyl-acrylamide (PAM-2), 3-furan-2-yl-N-o-tolylacrylamide (PAM-3), and3-furan-2-yl-N-phenylacrylamide (PAM-4), was teste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a53385f69a206320399bb28bd38068
https://doi.org/10.1016/j.biocel.2016.04.015
https://doi.org/10.1016/j.biocel.2016.04.015
Autor:
Daniela Braghiroli, Giulio Rastelli, Cinzia Citti, Giuseppe Ciccarella, Umberto Maria Battisti, Federica Ravazzini, Giuseppe Cannazza, Luca Pinzi, Giulia Puja
Publikováno v:
MedChemComm. 7:2410-2417
Benzothiadiazine type compounds (BTDs) have gained great attention for their potential therapeutic activity as nootropic and neuroprotective agents. BTDs, acting as AMPA positive allosteric modulators, potentiate the glutamatergic neurotransmission w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42764503fd3ec0b5446f4f08e83bb83b
https://doi.org/10.1039/c6md00440g
https://doi.org/10.1039/c6md00440g
Autor:
Hugo R. Arias, Giulia Puia, Piotr Popik, Federica Ravazzini, Agnieszka Potasiewicz, Agnieszka Nikiforuk, Tomasz Kos
Publikováno v:
British Journal of Pharmacology. 172:5123-5135
Background and Purpose α7 nicotinic acetylcholine receptors (α7 nAChRs) may represent useful targets for cognitive improvement. The aim of this study is to compare the pro-cognitive activity of selective α7-nAChR ligands, including the partial ago
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c20a8a790155dbe266211589065ad93
https://doi.org/10.1111/bph.13277
https://doi.org/10.1111/bph.13277
Publikováno v:
Journal of Chromatography B. 930:62-69
Neurosteroids (NSs) are well known modulators of neuronal activity and by binding to different neuronal receptors are responsible for a broad spectrum of biological and pathophysiological conditions. Here, a sensitive liquid chromatographic-electrosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::734b412edc585f2161f39873802f1160
https://doi.org/10.1016/j.jchromb.2013.04.035
https://doi.org/10.1016/j.jchromb.2013.04.035
Autor:
Giulia Puia, Maria Zappalà, Nicola Micale, Federica Ravazzini, Roberta Ettari, Rosanna Caputo, Calabrò Ml
Publikováno v:
Medicinal Chemistry Research. 22:6089-6095
This manuscript describes the synthesis of a new series of 2-amino-6-(trifluoromethoxy)benzoxazole derivatives (1–5) and a benzothiazine derivative (6) structurally related to riluzole, the only neuroprotective drug currently approved for the treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efb7217cd5004b0e6a88c55027409ce4
https://doi.org/10.1007/s00044-013-0594-4
https://doi.org/10.1007/s00044-013-0594-4
Autor:
Giulia Puja, Krzysztof Jozwiak, Cinzia Citti, Natalia Stasiak, Carlo Parenti, Umberto Maria Battisti, Michele Zoli, Luigino Troisi, Federica Ravazzini, Giuseppe Ciccarella, Giuseppe Cannazza, Daniela Braghiroli
5-Arylbenzothiadiazine type compounds acting as positive allosteric modulators of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPA-PAMs) have received particular attention in the past decade for their nootropic activity and lack o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e17116bed437e878f4a1117907082812
https://hdl.handle.net/11380/1116497
https://hdl.handle.net/11380/1116497
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
Changes in GABAergic inhibition occur during physiological processes, during response to drugs and in various pathologies. These changes can be achieved through direct allosteric modifications at the γ-aminobutyric (GABA) type A (GABAA) receptor pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55cba248e076c3256c57b5c642d6db46
Autor:
Daniela Braghiroli, Marina Carrozzo, Giulia Puia, Carlo Parenti, Giuseppe Cannazza, Cinzia Citti, Umberto Maria Battisti, Federica Ravazzini, Serena Perrone, Krzysztof Jozwiak, Aurelia Falchicchio, Luigino Troisi
Chiral 5-arylbenzothiadiazine derivatives have recently attracted particular attention because they exhibit an interesting pharmacological activity as AMPA receptor (AMPAr) positive modulators. However, investigations on their configurational stabili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cfae23b5b8f4d1b9aa068289a2708f6
http://www.journals.elsevier.com/bioorganic-and-medicinal-chemistry/
http://www.journals.elsevier.com/bioorganic-and-medicinal-chemistry/
Autor:
Battisti, Umberto M., Citti, Cinzia, Rastelli, Giulio, Pinzi, Luca, Puja, Giulia, Ravazzini, Federica, Ciccarella, Giuseppe, Braghiroli, Daniela, Cannazza, Giuseppe
Publikováno v:
MedChemComm; Dec2016, Vol. 7 Issue 12, p2410-2417, 8p