Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fatima de Campos-Buzzi"'
Autor:
David Rivero Tames, Xana Raquel Ortolan, Fatima de Campos-Buzzi, Rogério Corrêa, Telmo José Mezadri
Publikováno v:
Journal of Oral Research, Vol 6, Iss 8, Pp 209-215 (2017)
Aim. To evaluate the osteogenic potential of chalcones using the rat critical size calvarial defect. Methods. The chalcones were synthesized from acetophenone following the Claisen-Schmidt aldol condensation method by varying the substituted benzalde
Autor:
David Rivero Tames, Bruna Laís Tanello, Rogério Corrêa, Xana Raquel Ortolan, Telmo José Mezadri, María Helena Carpeggiani, Fatima de Campos-Buzzi
Publikováno v:
Journal of Oral Research, Vol 4, Iss 3, Pp 205-210 (2015)
Objective: The aim of this study is to evaluate the action of the synthetic chalcone 1-phenyl-3-(4-chlorophenyl)-2-propen-1-one to induce pulp healing in rats. Material and Methods: Sixty lower first molars of male Wistar rats were divided into 3 gro
Autor:
T. C. Tristão, Rosana Cé Bella Cruz, Rúbia Carvalho Gomes Corrêa, A. Bella Cruz, V. Cechinel Filho, Fatima de Campos-Buzzi
Publikováno v:
Arzneimittelforschung. 62:590-594
Chalcones constitute one of the major classes of natural products belonging to the flavonoid family, and they have been reported as having a range of important therapeutic activities, including some chalcones are effective as antimicrobial agents. Cu
Publikováno v:
Pharmaceutical Biology. 43:573-578
In the current study, we investigated the analgesic activity of a crude methanol extract and some fractions obtained from Hyeronima alchorneoides Allemao leaves and analyzed its phytochemical profile to determine active principles. All the fractions
Autor:
Rogério Corrêa, Valdir Cechinel-Filho, Pâmela Padaratz, Rivaldo Niero, Fatima de Campos-Buzzi, Mauricio Fracasso, Franco Delle Monache
Publikováno v:
Basicclinical pharmacologytoxicology. 105(4)
Chalcones represent an important group of natural or synthetic compounds with a variety of biological activities including antinociceptive and anti-inflammatory ones. The aim of this work was the synthesis of a new benzofuranone compound and evaluati
Akademický článek
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Autor:
Karina Louise S. Messias, Fátima de Campos-Buzzi, Luiz G. O. Fischer, Ângela Malheiros, Franco Delle Monache, Valdir Cechinel Filho
Publikováno v:
Química Nova, Vol 31, Iss 7, Pp 1747-1749 (2008)
This paper describes the isolation of five phytoconstituents from Marlierea tomentosa. The triterpenes α-amyrin (1) and β-amyrin (2), and the flavonoids quercitrin (3) and isoquercetin (4), were isolated from the leaves. The branches afforded the t
Externí odkaz:
https://doaj.org/article/19ce8c144e014893aa649b521086fd50