Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Roberta Sinisi"'
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100654- (2022)
An efficient synthetic route was set up to prepare in good scale M-108, a novel bicycle derivative recently identified as a potent and selective G9a inhibitor, potentially useful as anti-fibroadipogenic agent. In particular, a facile three-steps sequ
Externí odkaz:
https://doaj.org/article/541b77a011324d9aa43adcccd223c3a1
Autor:
Leda Ivanova Bencheva, Lorena Donnici, Luca Ferrante, Adolfo Prandi, Roberta Sinisi, Marilenia De Matteo, Pietro Randazzo, Matteo Conti, Pietro Di Lucia, Elisa Bono, Leonardo Giustini, Maria Vittoria Orsale, Alexandros Patsilinakos, Edith Monteagudo, Matteo Iannacone, Vincenzo Summa, Luca G. Guidotti, Raffaele De Francesco, Romano Di Fabio
Publikováno v:
Bioorganicmedicinal chemistry letters. 73
Chronic hepatitis B (CHB) is a major worldwide public health problem and novel anti-HBV therapies preventing liver disease progression to cirrhosis and hepatocellular carcinoma are urgently needed. Over the last several years, capsid assembly modulat
Autor:
Pietro Randazzo, Roberta Sinisi, Davide Gornati, Stefania Bertuolo, Leda Bencheva, Marilenia De Matteo, Martina Nibbio, Edith Monteagudo, Lorenzo Turcano, Valeria Bianconi, Giovanna Peruzzi, Vincenzo Summa, Alberto Bresciani, Chiara Mozzetta, Romano Di Fabio
Publikováno v:
Bioorganicmedicinal chemistry letters. 72
A new series of in vitro potent and highly selective histone methyl transferase enzyme G9a inhibitors was obtained. In particular, compound 2a, one the most potent G9a inhibitor identified, was endowed with >130-fold selectivity over GLP and excellen
Autor:
Adolfo Prandi, Luca Ferrante, Maria Veneziano, Mariana Gallo, Marco Ferrara, Leda Ivanova Bencheva, Antonella Cellucci, Nausicaa Mazzocchi, Pierfausto Seneci, Silvano Ronzoni, Andrea Menegon, Roberta Sinisi, Pietro Randazzo, Vincenzo Summa, Marilenia De Matteo, Romano Di Fabio
[Image: see text] Acid-sensing ion channels (ASICs) are a family of ion channels permeable to cations and largely responsible for the onset of acid-evoked ion currents both in neurons and in different types of cancer cells, thus representing a potent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8a3bad6284485d88304e25bccd2e07
http://hdl.handle.net/11588/828238
http://hdl.handle.net/11588/828238
Autor:
Paolo Lazzari, Matteo Zanda, Luca Pani, Alessandra Ghilardi, Stefania Ruiu, Roberta Sinisi, Monica Sani, Luciana Malpezzi
Publikováno v:
ChemMedChem. 4:1416-1420
Autor:
Françoise Pecker, Monica Sani, R. Parente, Gabriele Candiani, Roberta Sinisi, Matteo Zanda, Stefano Bellosta
Publikováno v:
Tetrahedron Letters. 46:6515-6518
The racemic α-trifluoromethyl-α-amino-β-sulfone hydroxamates 1 were synthesized by means of a nucleophilic addition of sulfur-stabilized carbanions to a N -Cbz imine of trifluoropyruvate ( 4 ). The free amino derivative 1a was the most potent inhi
Autor:
Marco Allarà, Francesco Piscitelli, Giancarlo Colombo, Ettore Novellino, Serena Pasquini, Vincenzo Di Marzo, Romano Silvestri, Alessia Ligresti, Chiara Bigogno, Giuseppe La Regina, Giulio Dondio, Marco Giulio Rozio, Roberta Sinisi, Antonella Brizzi, Federico Corelli, Noemi Fantini, Valerio Gatti, Mauro A.M. Carai, Antonio Lavecchia
Publikováno v:
European journal of medicinal chemistry 45 (2010): 5878–5886. doi:10.1016/j.ejmech.2010.09.053
info:cnr-pdr/source/autori:Silvestri, Romano; Ligresti, Alessia; La Regina, Giuseppe; Piscitelli, Francesco; Gatti, Valerio; Lavecchia, Antonio; Brizzi, Antonella; Pasquini, Serena; Allara, Marco; Fantini, Noemi; Carai, Mauro Antonio Maria; Bigogno, Chiara; Rozio, Marco Giulio; Sinisi, Roberta; Novellino, Ettore; Colombo, Giancarlo; Di Marzo, Vincenzo; Dondio, Giulio; Corelli, Federico/titolo:Synthesis and biological evaluation of new N-alkyl 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides as cannabinoid receptor ligands/doi:10.1016%2Fj.ejmech.2010.09.053/rivista:European journal of medicinal chemistry/anno:2010/pagina_da:5878/pagina_a:5886/intervallo_pagine:5878–5886/volume:45
info:cnr-pdr/source/autori:Silvestri, Romano; Ligresti, Alessia; La Regina, Giuseppe; Piscitelli, Francesco; Gatti, Valerio; Lavecchia, Antonio; Brizzi, Antonella; Pasquini, Serena; Allara, Marco; Fantini, Noemi; Carai, Mauro Antonio Maria; Bigogno, Chiara; Rozio, Marco Giulio; Sinisi, Roberta; Novellino, Ettore; Colombo, Giancarlo; Di Marzo, Vincenzo; Dondio, Giulio; Corelli, Federico/titolo:Synthesis and biological evaluation of new N-alkyl 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides as cannabinoid receptor ligands/doi:10.1016%2Fj.ejmech.2010.09.053/rivista:European journal of medicinal chemistry/anno:2010/pagina_da:5878/pagina_a:5886/intervallo_pagine:5878–5886/volume:45
A series of N-alkyl 1-ary1-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides were synthesized as new ligands of the human recombinant receptor hCB(1). n-Alkyl carboxamides brought out different SARs from the branched subgroup. Unsubstituted pyrrole deriv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c974bae0b899bbbe8fbd3a881d74bb2
http://hdl.handle.net/11588/415058
http://hdl.handle.net/11588/415058
Autor:
Monika Jagodzinska, Alessandro Volonterio, Matteo Zanda, Roberta Sinisi, Raffaella Maffezzoni, Florent Huguenot, Monica Sani, Gabriele Candiani
Publikováno v:
Fluorine in Medicinal Chemistry and Chemical Biology
info:cnr-pdr/source/autori:Sinisi R., Jagodzinska M., Candiani G., Huguenot F., Sani M., Volonterio A., Maffezzoni R., Zanda M./titolo:Fluorinated Inhibitors of Matrix Metalloproteinases/titolo_volume:/curatori_volume:/editore:/anno:2009
info:cnr-pdr/source/autori:Sinisi R., Jagodzinska M., Candiani G., Huguenot F., Sani M., Volonterio A., Maffezzoni R., Zanda M./titolo:Fluorinated Inhibitors of Matrix Metalloproteinases/titolo_volume:/curatori_volume:/editore:/anno:2009
The synthesis of potent inhibitors of matrix metalloproteinases (MMPs) bearing trifluoromethyl or difluoromethyl groups in purely aliphatic positions, and the effect of the incorporation of the fluoroalkyl functions on the inhibitory potency is prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::706ccdc2b9a616e58452cbe9e0e1e528
https://doi.org/10.1002/9781444312096.ch4
https://doi.org/10.1002/9781444312096.ch4
Autor:
Luca Bruché, Raffaella Maffezzoni, Nathalie Moussier, Monica Sani, Gabriele Candiani, Florent Huguenot, Matteo Zanda, Fiorenza Viani, Monika Jagodzinska, Roberta Sinisi
Publikováno v:
ChemInform. 38
Autor:
Matteo Zanda, Roberta Sinisi
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[37468-00-1] C3H2F3NO2 (MW 141.05) InChI = 1S/C3H2F3NO2/c4-3(5,6)1-2-7(8)9/h1-2H/b2-1+ InChIKey = FCKHHHXXJZMXBH-OWOJBTEDSA-N (reagent used as a three-carbon electrophile or dipolarophile) Physical Data: bp 80–85 °C; d 1.423 g cm−3. Solubility:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8b0d4c2818ccbcad23dbda67d60c7c5
https://doi.org/10.1002/9780470842898.rn00708
https://doi.org/10.1002/9780470842898.rn00708