Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Carlos Alberto de Simone"'
Autor:
Ana Maria Alves Souza, Simone Torres Pádua Walfrido, Lúcia Fernanda Costa Leite, Maria Carmo Alves Lima, Suely Lins Galdino, Ivan Rocha Pitta, José Maria Barbosa Filho, Carlos Alberto De Simone, Javier Alcides Ellena
Publikováno v:
Química Nova, Vol 33, Iss 3, Pp 562-565 (2010)
This article describes the synthesis of the new (2Z)-2-(4-methoxybenzylidene)-6-nitro-4H -benzo[1,4]thiazin-3-one, (2Z)-2-(4-methoxybenzylidene)-4-methyl-6-nitro-4H-benzo[1,4]thiazin-3-one, (2Z)-6-amino-2-(4-methoxybenzylidene)-4H -benzo[1,4]thiazin-
Externí odkaz:
https://doaj.org/article/a9bd52f486e549508360367e2efb7a51
Autor:
Gerardo Magela Vieira Júnior, Hilris Rocha e Silva, Thaís Chaves Bittencourt, Mariana H. Chaves, Carlos Alberto de Simone
Publikováno v:
Química Nova, Vol 30, Iss 7, Pp 1658-1662 (2007)
This paper describes the isolation of the furanocassane-type diterpene, named vinhaticoic acid, along with beta-farnesene and spatulenol from fruit shells of D. lacunifera. Structural determinations were accomplished by chemical derivatization and sp
Externí odkaz:
https://doaj.org/article/7c05d3fd311248c592962ac23a941aae
Autor:
Carlos Alberto de Simone
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
A técnica de difração de raios X por monocristais foi utilizada na resolução dos problemas resumidos a seguir. 1) Complexos de lantanóides: 1.1) Estrutura cristalina e molecular do complexo de coordenação {(Nd(NCS)3(HMPA)3]}{(Nd(NCS)3(HMPA)4]
Autor:
Carlos Alberto de Simone
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
A estrutura da florencita foi refinada pelo método de mínimos quadrados, utilizando dados experimentais obtidos através do método de Debye-Scherrer. A coleta dos dados das intensidades integradas foi feita através da leitura do difratograma de p
Autor:
Cleverson N. Pinto, Adolfo Carlos Barros de Souza, Tiago T. Guimarães, Carlos Alberto De Simone, Antonio V. Pinto, Eufrânio N. da Silva Júnior, Maria do Carmo F. R. Pinto
Publikováno v:
Tetrahedron Letters. 50:1550-1553
In the last few years, natural quinones of the lapachol group have been used as starting points for the preparation of several bioactive heterocyclic compounds. Herein, we announce that lapachones, derivatives of lapachol, under certain conditions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ac0d2a159d51e341fabb9218f248eef
https://doi.org/10.1016/j.tetlet.2009.01.058
https://doi.org/10.1016/j.tetlet.2009.01.058
Autor:
Cleverson N. Pinto, Adolfo Carlos Barros de Souza, Tiago T. Guimarães, Carlos Alberto De Simone, Antonio V. Pinto, Eufrânio N. da Silva Júnior, Maria do Carmo F. R. Pinto
Publikováno v:
ChemInform. 40
In the last few years, natural quinones of the lapachol group have been used as starting points for the preparation of several bioactive heterocyclic compounds. Herein, we announce that lapachones, derivatives of lapachol, under certain conditions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7bcd2a4fe6df0d3a1b04a5a0782ab0c
https://doi.org/10.1002/chin.200929089
https://doi.org/10.1002/chin.200929089
Autor:
Rubem F. S. Menna-Barreto, Carlos Alberto De Simone, Antonio V. Pinto, Daniel V. Teixeira, Solange L. de Castro, Vitor F. Ferreira, Eufranio N. Jr. da Silva, Maria do Carmo F. R. Pinto, Raphael S. F. Silva, Maria Cecília B. V. de Souza
Publikováno v:
ChemInform. 39
[1,2,3]-Triazole derivatives of nor-beta-lapachone were synthesized and assayed against the infective bloodstream trypomastigote form of Trypanosoma cruzi, the etiological agent of Chagas disease. All the derivatives were more active than the origina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f46f25938a462d30e686a69529592da
https://doi.org/10.1002/chin.200852201
https://doi.org/10.1002/chin.200852201
Autor:
Antonio V. Pinto, Raphael S. F. Silva, Solange L. de Castro, Vitor F. Ferreira, Maria do Carmo F. R. Pinto, Eufranio N. Jr. da Silva, Daniel V. Teixeira, Carlos Alberto De Simone, Maria Cecília B. V. de Souza, Rubem F. S. Menna-Barreto
Publikováno v:
European journal of medicinal chemistry. 43(8)
[1,2,3]-Triazole derivatives of nor-beta-lapachone were synthesized and assayed against the infective bloodstream trypomastigote form of Trypanosoma cruzi, the etiological agent of Chagas disease. All the derivatives were more active than the origina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cffebcd8303d536196cd42ca339ea812
https://pubmed.ncbi.nlm.nih.gov/18045742
https://pubmed.ncbi.nlm.nih.gov/18045742
Autor:
Gustavo L. Santos, Valéria R. S. Malta, Raphael S. F. Silva, Antonio V. Pinto, Solange L. de Castro, Carlos Alberto De Simone, Maria de Carmo F. R. Pinto, Elaine Maria Frade Costa, Ursula L. T. Trindade, Daniel V. Teixeira
Publikováno v:
ChemInform. 37
Four new naphthofuranquinones, obtained from 2-hydroxy-3-allyl-naphthoquinone (1) and nor-lapachol (2), have their structures established by physical and X-ray analysis and their activity evaluated against Trypanosoma cruzi. Compounds 3 and 4 were ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::094c5b558c3d63c7c95632f3804249e1
https://doi.org/10.1002/chin.200638105
https://doi.org/10.1002/chin.200638105
Autor:
Carlos Alberto De Simone, Raphael S. F. Silva, Antonio V. Pinto, Gustavo L. Santos, Maria de Carmo F. R. Pinto, Elaine Maria Frade Costa, Ursula L. T. Trindade, Daniel V. Teixeira, Solange L. de Castro, Valéria R. S. Malta
Publikováno v:
European journal of medicinal chemistry. 41(4)
Four new naphthofuranquinones, obtained from 2-hydroxy-3-allyl-naphthoquinone (1) and nor-lapachol (2), have their structures established by physical and X-ray analysis and their activity evaluated against Trypanosoma cruzi. Compounds 3 and 4 were ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e3e32a739b7edcdbec52532d4a5fc40
https://pubmed.ncbi.nlm.nih.gov/16500733
https://pubmed.ncbi.nlm.nih.gov/16500733