Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yolanda Sainz"'
Autor:
Gabriela Aguirre, Alejandra Gerpe, Carmen Ochoa de Ocariz, Juan José Nogal, Yolanda Sainz, Hugo Cerecetto, Ana Denicola, David Montero, Mariana Boiani, Mercedes González, José Antonio Escario
Publikováno v:
Archiv der Pharmazie. 337:259-270
The syntheses and biological evaluation of the first anti-protozoa imidazole N-oxide and benzimidazole N-oxide and their derivatives are reported. They were tested in vitro against two different protozoa, Trypanosoma cruzi and Trichomonas vaginalis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c4b333d671821de511f95fc548498a2
https://doi.org/10.1002/ardp.200300840
https://doi.org/10.1002/ardp.200300840
Autor:
Oscar E. Piro, Hugo Cerecetto, Mercedes González, Alejandra Gerpe, Eduardo E. Castellano, Yolanda Sainz
Publikováno v:
Synthesis. 2004:2678-2684
A new synthetic procedure of 1-alkyl(aryl)-1H-4-methylimidazole N 3 -oxide derivatives by cyclocondensation of α-amine-oximes and orthoesters was studied. Low yields in the cyclization process were the result of predominant Z-stereoisomer around the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5af240e7947cf2f1333a7110e649c7ad
https://doi.org/10.1055/s-2004-831212
https://doi.org/10.1055/s-2004-831212
Publikováno v:
Il Farmaco. 53:570-573
Tuberculosis, an ancient disease undergoing recent control by public hygiene and drug therapy, has experienced a recrudescence throughout the world. New and effective therapies are rapidly needed to combat infections caused by these strains. Some new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f658b3705f82e248303e67e8f9329a23
https://doi.org/10.1016/s0014-827x(98)00067-6
https://doi.org/10.1016/s0014-827x(98)00067-6
Autor:
A. López de Cerain, Yolanda Sainz, A. J. Barker, Antonio Monge, S. Narro, J. A. Palop, E. Hamilton, V. Senador, F. J. Martinez Crespo, Mercedes González
Publikováno v:
Journal of Heterocyclic Chemistry. 33:1671-1677
Several quinoxaline 1,4-di-N-oxides have been shown to be efficient and selective cytotoxins for hypoxic cells. We present now a series of 4-cyano-2-oxo-1,2,4-oxadiazolo[2,3-a]quinoxaline 5-N-oxides 2a-2k. They were prepared starting from 3-amino-2-q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::864b01907dcf5d2a41facfacc5c1ed70
https://doi.org/10.1002/jhet.5570330620
https://doi.org/10.1002/jhet.5570330620
Autor:
Estrella G. Alvarez, Ana M. Ochoa de Retana Mendibil, Gildardo Rivera Sánchez, Yolanda Sainz Sánchez, Argimiro Rivero, Teresa Alvarez, José Ignacio RecaldeIrurzun, Victor MartínezMerino, Mercedes González, Lídia Moreira Lima, Silvia Pérez Silanes, Luis Orts, Estefanía Berjón, Hugo Cerecetto, Ignacio A. Moraza, Patricio H. Gómez, Juan Carlos del Castillo, Silvia G. Ruiz
Publikováno v:
Revista Virtual de Química. 5
In this special issue of the Virtual Journal of Chemistry (“Revista Virtual de Quimica”, RVq), dedicated to record the retirement of Dr Antonio Monge – Full Professor at the University of Navarra and Scientific Director of the Center for Applie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6762472a6e0ea436f60f01569d7aa077
https://doi.org/10.5935/1984-6835.20130086
https://doi.org/10.5935/1984-6835.20130086
Autor:
A. López de Cerain, E. Hamilton, J. A. Palop, A. Pinol, A. J. Barker, Mercedes González, S. Narro, Antonio Monge, F. J. Martinez‐Crespo, Yolanda Sainz
Publikováno v:
Scopus-Elsevier
Starting with 3-amino-2-quinoxalinecarbonitrile 1,4-dioxide 1, a new series of quinoxaline derivatives was prepared through chemical modifications of the 2-cyano and 3-amino groups. Nitration of 3-amino-2-quin-oxalinecarbonitrile 3 afforded the 7-nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad5853d8427249cbd0044988bc82924
https://doi.org/10.1002/jhet.5570310506
https://doi.org/10.1002/jhet.5570310506
Autor:
A. J. Barker, J. A. Palop, S. Narro, Antonio Monge, Yolanda Sainz, A. Pinol, A. López de Cerain, E. Hamilton, Mercedes González, F. J. Martinez‐Crespo
Publikováno v:
ChemInform. 26
Starting with 3-amino-2-quinoxalinecarbonitrile 1,4-dioxide 1, a new series of quinoxaline derivatives was prepared through chemical modifications of the 2-cyano and 3-amino groups. Nitration of 3-amino-2-quin-oxalinecarbonitrile 3 afforded the 7-nit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58c5c36b6657b57b29a7f7f3f40b1c85
https://doi.org/10.1002/chin.199514177
https://doi.org/10.1002/chin.199514177
Autor:
A. López de Cerain, S. Narro, F. J. Martinez‐Crespo, J. A. Palop, Mercedes González, E. Hamilton, Yolanda Sainz, A. J. Barker, Antonio Monge
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aebfcb3d8f84557a98dc0ff97a65284
https://doi.org/10.1002/chin.199551196
https://doi.org/10.1002/chin.199551196
Autor:
A. López de Cerain, E. Hamilton, V. Senador, Mercedes González, J. A. Palop, S. Narro, Yolanda Sainz, A. J. Barker, Antonio Monge, F. J. Martinez Crespo
Publikováno v:
ChemInform. 28
Several quinoxaline 1,4-di-N-oxides have been shown to be efficient and selective cytotoxins for hypoxic cells. We present now a series of 4-cyano-2-oxo-1,2,4-oxadiazolo[2,3-a]quinoxaline 5-N-oxides 2a-2k. They were prepared starting from 3-amino-2-q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::947e950800bc0d70e367d417c4072a9a
https://doi.org/10.1002/chin.199725151
https://doi.org/10.1002/chin.199725151
Publikováno v:
ChemInform. 30
Tuberculosis, an ancient disease undergoing recent control by public hygiene and drug therapy, has experienced a recrudescence throughout the world. New and effective therapies are rapidly needed to combat infections caused by these strains. Some new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4b8dddea71de51db53adec56b50e67c
https://doi.org/10.1002/chin.199922159
https://doi.org/10.1002/chin.199922159