Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Alessandro Ettorre"'
Autor:
Roberto Chiesa, Alessandro Ettorre, Luigi De Nardo, Andrea Serafini, Alessandro C. Scalia, Stefania Cometa, Lia Rimondini, Agnese D’Agostino, Francesca Tana, Elvira De Giglio, Matteo Pavarini, Andrea Cochis
Publikováno v:
Biomedical Materials. 16:045016
Cytocompatible bioactive surface treatments conferring antibacterial properties to osseointegrated dental implants are highly requested to prevent bacteria-related peri-implantitis. Here we focus on a newly designed family of mesoporous coatings base
The paper applies the cluster analysis methodology to thermoplastic Polyphenylene sulphide (PPS) carbon woven composites. The experimental quasi-static tensile tests were assisted by: a digital camera for digital image correlation (DIC) evaluation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd70ce8cb3bf067543bd510676fbe8e4
http://hdl.handle.net/11311/1027245
http://hdl.handle.net/11311/1027245
Autor:
Marina Porcelloni, Elena Marastoni, Maria Altamura, Rose-Marie Catalioto, Sandro Giuliani, Carlo Alberto Maggi, Sandro Mauro, Stefania Meini, Cristina Rossi, Piero D’Andrea, Alessandro Ettorre, Daniela Fattori
Publikováno v:
Journal of Medicinal Chemistry. 53:4148-4165
As part of a project aimed at the identification of a series of small, orally available antagonists for the hNK(2) receptor, starting from one of our capped dipeptide libraries, we succeeded in the chemical optimization of the first identified leads,
Autor:
Marina Porcelloni, Stefania Meini, Andrea Madami, Sandro Giuliani, Maria Altamura, Cristina Rossi, Alessandro Ettorre, Daniela Fattori, Alessandro Sisto, Piero D’Andrea
Publikováno v:
ChemMedChem. 3:1048-1060
The NK(2) receptor belongs to the family of tachykinin neurotransmitters. It has been reported to be involved in several pathological conditions, and selective antagonists are potentially useful drugs for the treatment of asthma, irritable bowel synd
Autor:
Piero D’Andrea, Alessandro Ettorre, Rose Marie Catalioto, Maria Altamura, Sandro Giuliani, Carlo Alberto Maggi, Sandro Mauro, Daniela Fattori, Cristina Rossi, Marina Porcelloni
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:1807-1809
Starting from in-house capped tripeptide libraries, we have developed two series of compounds as potent antagonists of the hNK2 receptor with a reduced peptide character. These two series maintained a crucial amide bond, which could not be methylated
Autor:
Sandra Bartoli, Amalia Cipollone, Mario Bigioni, Marco Berettoni, Alessandro Ettorre, Carlo Alberto Maggi, Christopher I. Fincham, Federica Nardelli, Marina Porcelloni, Daniela Fattori, Paola Paoli, Patrizia Rossi, Monica Binaschi, Sandro Mauro, Marielle Paris, Elena Marastoni, Massimo Parlani
Publikováno v:
Bioorganicmedicinal chemistry letters. 25(7)
In the search for a new class of histone deacetylase inhibitors, we prepared a series of very simple benzofused hydroxamic acids to find an anchoring fragment of minimal molecular weight: they showed very good ligand efficiencies. Following these fin
Autor:
Paolo La Colla, Biancamaria Bruno, Giovanni Greco, E. Pagnozzi, Ettore Novellino, Anna Giulia Loi, and Franca Scintu, Silvio Massa, Romano Silvestri, Marino Artico, Alessandro Ettorre
Publikováno v:
Journal of Medicinal Chemistry. 43:1886-1891
Pyrrolyl aryl sulfones (PASs) have been recently reported as a new class of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) inhibitors acting at the non-nucleoside binding site of this enzyme (Artico, M.; et al. J. Med. Chem. 1
Publikováno v:
Scopus-Elsevier
A possible reaction route for Ir(H)(Cl2)(P-i-Pr3)3 (4) is proposed. The complexes [HP-i-Pr3]2[IrCl6] (1), [HP-i-Pr3]2[Ir2Cl8(P-i-Pr3)] (2) and [HP-i-Pr3][Ir2Cl7(P-i-Pr3)2] (3) were investigated. It is shown that 1, 2 and 3 are possible intermediates
Autor:
Valeria Menchise, Fernando Formaggio, Laura Graci, Gian Maria Bonora, Michele Saviano, Ettore Benedetti, Benedetto Di Blasio, Claudio Toniolo, Giovanni Valle, Alessandro Ettorre, Carlo Pedone, Marco Crisma, Rosa Iacovino
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :2023-2032
A complete series of N- and C-blocked, monodispersed homo-oligopeptides to the pentamer level from 1-aminocycloheptane-1-carboxylic acid (Ac7c), an α-amino acid conformationally restricted through Ciα ←→ Ciα cyclization, and three tripeptides
Autor:
Sandro Mauro, Daniela Fattori, Alessandro Ettorre, Sandra Bartoli, Christopher I. Fincham, Massimo Parlani, Carlo Alberto Maggi, Marina Porcelloni, Federica Nardelli, Elena Marastoni, Amalia Cipollone, Monica Binaschi, Marielle Paris, Mario Bigioni, Marco Berettoni
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(14)
In the search for a new class of histone deacetylase inhibitors, we prepared a series of simple benzofused hydroxamic acids to find an anchoring fragment of minimal molecular weight. These initial hits, all belonging to the benzothiophene class, show