Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Alessandro K, Jordão"'
Publikováno v:
SynOpen, Vol 07, Iss 03, Pp 371-373 (2023)
Externí odkaz:
https://doaj.org/article/a0c925d3a0ed4b91a29f69f25812b85c
Publikováno v:
SynOpen, Vol 06, Iss 03, Pp 208-210 (2022)
Externí odkaz:
https://doaj.org/article/de411c2a86fd4bf7a448cb56efb1c76e
Autor:
Olívia B. O. Moreira, Maria Clara R. Freitas, Karynne C. Souza, Alessandro K. Jordão, Jackson A. L. C. Resende
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 738-741 (2019)
In the molecular structure of the title compound, C10H10N4O2·H2O, the angle between the triazole and arene rings is 87.39 (5)°. The water of crystallization connects the molecules in the crystal packing. The crystal structure exhibits N—H...O, O
Externí odkaz:
https://doaj.org/article/d17196b5341e45418b9ea803d2da03a6
Autor:
Douglas VQ. Nunes, Cristiane A. Costa, Graziele F. De Bem, Viviane SC. Cordeiro, Izabelle B. Santos, Lenize CRM. Carvalho, Alessandro K. Jordão, Anna C Cunha, Vitor F Ferreira, Roberto S Moura, Angela C. Resende, Dayane T. Ognibene
Publikováno v:
Clinical and Experimental Hypertension, Vol 40, Iss 8, Pp 721-729 (2018)
Tempol, a superoxide dismutase-mimetic drug, has been shown to attenuate radical-induced damage, exerting beneficial effects in the animal models of oxidative stress and hypertension. This study evaluated the effect of Tempol on renal structural and
Externí odkaz:
https://doaj.org/article/85be16b72df54a83b666040a786925e7
Autor:
Estela M. G. Lourenço, Júlia M. Fernandes, Vinícius de F. Carvalho, Raphael Grougnet, Marco A. Martins, Alessandro K. Jordão, Silvana M. Zucolotto, Euzébio G. Barbosa
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2020)
Natural products are considered an important source of bioactive compounds especially in biodiversity-rich countries like Brazil. The identification of potential targets is crucial to the development of drugs from natural sources. In this context, in
Externí odkaz:
https://doaj.org/article/c188901e3ca045b294d5cfc76a6422fe
Publikováno v:
SynOpen. :208-210
Autor:
Priscila Bianca Borges Ferrari, Carlos Itsuo Yamamoto, Antonio S. Mangrich, Alessandro K. Jordão, Vitor F. Ferreira, Juliana Schultz, Anna C. Cunha
Publikováno v:
Revista Virtual de Química. 13:900-909
O objetivo deste estudo foi identificar substâncias adicionadas ao biodiesel capazes de minimizar as reacoes de oxidacao, impedindo o inicio ou antecipando o fim das reacoes de oxidacao. A espectroscopia EPR foi utilizada para identificar e caracter
Autor:
Anna C. Cunha, Alessandro K. Jordão, Maria C. B. V. de Souza, Vitor F. Ferreira, Maria C. B. de Almeida, James L. Wardell, Edward R. T. Tiekink
Publikováno v:
IUCrData, Vol 1, Iss 1, p x152447 (2016)
In the title compound, C10H10Cl2N4O, the hydroxy group and benzene ring are disposed to opposite sides of the central 1,2,3-triazolyl ring. The dihedral angle between the five- and six-membered rings is 87.51 (12)°, and the C—O bond of the hydroxy
Externí odkaz:
https://doaj.org/article/e5eb77558da4428d9b7b975fabed1d7e
Autor:
Anna C. Cunha, Alessandro K. Jordão, Maria C. B. V. de Souza, Vitor F. Ferreira, Maria C. B. de Almeida, James L. Wardell, Edward R. T. Tiekink
Publikováno v:
IUCrData, Vol 1, Iss 1, p x160038 (2016)
The title compound, C10H10N4O, is twisted about the Nring—Namine bond with the dihedral angle between the 1,2,3-triazolyl and N-bound phenyl rings being 79.14 (9)°. The C-bound aldehyde group is coplanar with the triazolyl ring, with the N—C—C
Externí odkaz:
https://doaj.org/article/1d3af62912dd4e1ea391d19aec6c3e6d
Autor:
Anna C. Cunha, Carolina Q. Sacramento, Jackson A. L. C. Resende, Thiago Moreno L. Souza, Maria G. F. Vaz, Rafael A. Allão Cassaro, Alessandro K. Jordão, Vitor F. Ferreira, Jessica Costa, Juliana L. Abrantes
Publikováno v:
Molecular Diversity. 25:2035-2043
HSV disease is distributed worldwide. Anti-herpesvirus drugs are a problem in clinical settings, particularly in immunocompromised individuals undergoing herpes simplex virus type 1 infection. In this work, 4-substituted-1,2,3-1H-1,2,3-triazole linke