Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sandro Mauro"'
Autor:
Sandro Mauro Guirro
Publikováno v:
Revista Pegada Eletrônica, Vol 2, Iss 1 (2011)
Atualmente, vêm ocorrendo mudanças no campo brasileiro, principalmente nas propriedades localizadas próximas a malha urbana da cidade. Esse processo se verifica com mais intensidade em cidades como Campinas, Sorocaba, Jundiaí entre outras cidades
Externí odkaz:
https://doaj.org/article/41bda5ed02da49bba65e71fbb445eb2e
Autor:
Temístocles de Sousa Luz, Fagner Bertholdi Fraga, Rubson Mação Camporez, Sandro Mauro de Carvalho, Sandro Souza
Publikováno v:
ABM Proceedings.
Autor:
Rubson Mação Camporez, Marcelo Camargo Severo de Macêdo, Sandro Mauro de Carvalho, Athos Rhein Martins, Temístocles de Souza Luz
Publikováno v:
ABM Proceedings.
Autor:
Victor Pizetta David, Pablo Altoé Amorim, Luiz Henrique Simões dos Reis, Sandro Mauro de Carvalho
Publikováno v:
Anais do Congresso Anual da ABM.
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:
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:
Monica Muratori, Carla Palma, Annalisa Lippi, Sandro Mauro, Carlo Alberto Maggi, Marco Criscuoli
Publikováno v:
European Journal of Pharmacology. 409:93-101
The racemate compound MEN 11066 (1-[(benzofuran-2-yl)(4′-cyanophenyl)methyl]-1 H -1,2,4-triazole) and its enantiomers, (+)-MEN 11623 and (−)-MEN 11622, showed potent and selective aromatase activity on human placental microsomes. In addition, to
Autor:
Antonio Triolo, Laura Quartara, Beatrice Anichini, Gaetano Fabbri, Sandro Mauro, Carlo Alberto Maggi, Renzo Ricci, Maria Altamura, Giuseppe Balacco
Publikováno v:
Journal of Peptide Science. 6:612-620
An efficient synthesis of the cyclic decapeptide MEN 11270 [H-DArg1-Arg2 Pro3-Hyp4-Gly5-Thi6-Dab7-DTic8-Oic9-Arg10 c(7gamma - 10alpha)] was developed. Two three-dimensional orthogonal strategies were applied and compared: Fmoc/Tos/Boc (procedure A) a
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