Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Catarina de Nigris Del Cistia"'
Autor:
Gabriela Alves de Souza, Soraia John da Silva, Catarina de Nigris Del Cistia, Paulo Pitasse-Santos, Lucas de Oliveira Pires, Yulli Moraes Passos, Yraima Cordeiro, Cristiane Martins Cardoso, Rosane Nora Castro, Carlos Mauricio R. Sant’Anna, Arthur Eugen Kümmerle
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 631-637 (2019)
A series of 3-substituted-7-aminoalcoxy-coumarin was designed and evaluated as cholinesterase inhibitors and antioxidants. All compounds were effective in inhibiting AChE with potencies in the nanomolar range. The 3-(4-(dimethylamino)phenyl)-7-aminoe
Externí odkaz:
https://doaj.org/article/e9dead6f6ad94242a6049c23caa5acd4
Autor:
Vitor Sueth-Santiago, Julliane de B B Moraes, Eliomara Sousa Sobral Alves, Marcos André Vannier-Santos, Célio G Freire-de-Lima, Rosane N Castro, Gustavo Peron Mendes-Silva, Catarina de Nigris Del Cistia, Luma Godoy Magalhães, Adriano Defini Andricopulo, Carlos Mauricio R Sant Anna, Debora Decoté-Ricardo, Marco Edilson Freire de Lima
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162926 (2016)
Curcumin (CUR) is the major constituent of the rhizomes of Curcuma longa and has been widely investigated for its chemotherapeutic properties. The well-known activity of CUR against Leishmania sp., Trypanosoma brucei and Plasmodium falciparum led us
Externí odkaz:
https://doaj.org/article/31a4dbc55d7b4810b05eb1639ba40e60
Autor:
Aurea Echevarria, Carlos Maurício R. Sant'Anna, Catarina de Nigris Del Cistia, Daniel Rosa da Silva, Claudio E. Rodrigues-Santos, Andressa Esteves-Souza
Publikováno v:
Molecules, Vol 17, Iss 11, Pp 12882-12894 (2012)
A new series of asymmetrically N,N'-substituted ureas 20–25 was prepared using solvent free conditions, which is an eco-friendly methodology, starting with Schiff bases derived from cinnamaldehyde and p-substituted anilines, which are subsequently
Externí odkaz:
https://doaj.org/article/767608b250cd47fcade3e19df222e96c
Autor:
Aurea Echevarria, William Queiroz Felippe, Catarina de Nigris Del Cistia, Vitor dos Santos Almeida, Guilherme P. Guedes, Carlos Mauricio R. Sant'Anna, Igor Resendes Barbosa, Ana Paula Pereira da Silva
Publikováno v:
Spectroscopy Letters. 54:607-618
The 1H and 13C nuclear magnetic resonance spectra of N2,N4,N6-triphenethyl-1,3,5-triazine-2,4,6-triamine show features that suggest the hindered rotation about the carbon-nitrogen bond. A dynamic e...
Autor:
Arthur Eugen Kümmerle, Gabriela Alves de Souza, Renata Barbosa Lacerda, Thiago Moreira Pereira, Catarina de Nigris Del Cistia, Daiana Portella Franco, Sabrina Neves Santos, Carlos Mauricio R. Sant'Anna
Publikováno v:
RSC advances. 9(35)
Herein we describe the development of an efficient one-pot regioselective synthesis protocol to obtain N-protected or N-deprotected 1,5-diaryl-3-amino-1,2,4-triazoles from N-acyl-N-Boc-carbamidothioates. This improved protocol using microwave irradia
Autor:
Paulo Pitasse-Santos, Yulli M. Passos, Rosane Nora Castro, Yraima Cordeiro, Soraia John da Silva, Carlos Mauricio R. Sant'Anna, Catarina de Nigris Del Cistia, Lucas de Oliveira Pires, Gabriela Alves de Souza, Arthur Eugen Kümmerle, Cristiane Martins Cardoso
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 631-637 (2019)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
A series of 3-substituted-7-aminoalcoxy-coumarin was designed and evaluated as cholinesterase inhibitors and antioxidants. All compounds were effective in inhibiting AChE with potencies in the nanomolar range. The 3-(4-(dimethylamino)phenyl)-7-aminoe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a8ea7bf615aacfe4fcf1acaba5887c
Autor:
Aurea Echevarria, Cláudio E. Rodrigues-Santos, Catarina de Nigris Del Cistia, Viviane dos Santos Faiões, Eduardo Caio Torres-Santos, Carlos Mauricio R. Sant'Anna, Jorge Luiz R. de Melos
Publikováno v:
European Journal of Medicinal Chemistry. 103:409-417
A series of eleven 3,4-methylenedioxyde-6-X-benzaldehyde-thiosemicarbazones (16–27) was synthesised as part of a study to search for potential new drugs with a leishmanicidal effect. The thiosemicarbazones, ten of which are new compounds, were prep
Autor:
Mariana da Silva Santos, Magna Suzana Alexandre-Moreira, Vinicius Tomaz Gonçalves, Catarina de Nigris Del Cistia, João Batista Neves DaCosta, Carolina Barbosa Brito da Matta, Carlos Mauricio R. Sant'Anna, Aline Cavalcanti de Queiroz
Publikováno v:
European Journal of Medicinal Chemistry. 101:1-12
As part of a program to develop new drugs for the treatment of neglected diseases, new dialkylphosphorylhydrazones were synthesized and evaluated against the trypanosomatid parasites Leishmania braziliensis and Leishmania amazonensis . The synthesis
Autor:
Carlos Mauricio R. Sant´Anna, Catarina de Nigris Del Cistia, Adriano D. Andricopulo, Eliomara Sousa Sobral Alves, Marcos A. Vannier-Santos, Marco Edilson Freire de Lima, Debora Decote-Ricardo, Gustavo Peron Mendes-Silva, Luma G. Magalhães, Rosane Nora Castro, Celio Geraldo Freire-de-Lima, Vitor Sueth-Santiago, Julliane de Brito Braz Moraes
Publikováno v:
PLoS ONE
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE, Vol 11, Iss 9, p e0162926 (2016)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE, Vol 11, Iss 9, p e0162926 (2016)
Curcumin (CUR) is the major constituent of the rhizomes of Curcuma longa and has been widely investigated for its chemotherapeutic properties. The well-known activity of CUR against Leishmania sp., Trypanosoma brucei and Plasmodium falciparum led us
Autor:
Manoel Odorico de Moraes, Carlos Mauricio R. Sant'Anna, Macia C. S. de Almeida, Telma L. G. Lemos, Francisco Stefânio Barreto, Raimundo Braz-Filho, Paulo Riceli Vasconcelos Ribeiro, Luciana G. S. Souza, Kirley Marques Canuto, Catarina de Nigris Del Cistia
Publikováno v:
Journal of the Brazilian Chemical Society.
Four new alkaloids, Brazoides A-D, together with three known compounds squalene, β-sitosterol and lupeol, were isolated from leaves of Justicia gendarussa. These structures were established by spectrometric techniques, mainly high-resolution electro