Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Mercedes Villarroya"'
Publikováno v:
Pflügers Archiv - European Journal of Physiology. 470:187-198
In this review, we show how chromaffin cells have contributed to evaluate neuroprotective compounds with diverse mechanisms of action. Chromaffin cells are considered paraneurons, as they share many common features with neurons: (i) they synthesize,
Autor:
María Isabel Rodríguez-Franco, Mariana P. Arce, Santiago Conde, Concepción Pérez, Mercedes Villarroya, Rafael León, Leticia Monjas, Javier Egea, Carmen Gil, Manuela G. López
Publikováno v:
European Journal of Medicinal Chemistry, 130, 60-72. ELSEVIER MASSON, CORPORATION OFFICE
Digital.CSIC. Repositorio Institucional del CSIC
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Digital.CSIC. Repositorio Institucional del CSIC
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Supplementary data associated with this article can be found in the online version, at http://dx.doi.org/10.1016/j.ejmech.2017.02. 034. These data include MOL files and InChiKeys of the most important compounds described in this article.
Previou
Previou
Autor:
Mercedes Villarroya, Laura González-Lafuente, Francisco J. Martínez-Sanz, Martín Estrada, Abdelouahid Samadi, Cristóbal de los Ríos, María Isabel Rodríguez-Franco, José Marco-Contelles, Rocío Lajarín-Cuesta, Alejandro Romero, Silvia Lorrio, Manuela G. López
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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ITH12246 (ethyl 5-amino-2-methyl-6,7,8,9-tetrahydrobenzo[b][1,8] naphthyridine-3-carboxylate) is a 1,8-naphthyridine described to feature an interesting neuroprotective profile in in vitro models of Alzheimer's disease. These effects were proposed to
Autor:
M. Carmo Carreiras, José Marco-Contelles, Manuela G. López, Alejandro Romero, Cristóbal de los Ríos, María-Luisa Jimeno, Abdelouahid Samadi, Daniel Silva, Eduarda Mendes, Mourad Chioua, Mercedes Villarroya
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The synthesis and pharmacological analyses of a number of pyrazolo[3,4-b]quinoline and benzo[b]pyrazolo[4,3-g][1,8]naphthyridine derivatives are reported. We have synthesized the diversely substituted tacrine analogues 1-6, by Friedländer-type react
Autor:
José Marco-Contelles, Laura González-Lafuente, Maria Dolores Martin-de-Saavedra, Abdelouahid Samadi, Mourad Chioua, Agatha Bastida, Mercedes Villarroya, Laura del Barrio, Cristóbal de los Ríos, Luis Gandía, Inés Colmena, Carolina Valderas, Manuela G. López, Alejandro Romero
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:122-133
The synthesis, biological assessment, and molecular modelling of new tacrine analogues 11–22 is described. Compounds 11–22 have been obtained by Friedlander-type reaction of 2-aminopyridine-3-carbonitriles 1–10 with cyclohexanone or 1-benzyl-4-
Autor:
Isabel Iriepa, Antonio G. García, Alejandro Romero, Mercedes Villarroya, José Marco-Contelles, Manuela G. López, Ignacio Moraleda, Rafael León, Abdelouahid Samadi, Enrique Gálvez, Cristóbal de los Ríos, Javier Egea
Publikováno v:
Journal of Medicinal Chemistry. 53:5129-5143
1,8-Naphthyridine derivatives related to 17 (ITH4012), a neuroprotective compound reported by our research group, have been synthesized. In general, they have shown better inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) th
Autor:
Xavier Barril, Antonio G. García, Oscar Huertas, F. Javier Luque, Mercedes Villarroya, Rafael León, Cristóbal de los Ríos, Manuela G. López, José Marco-Contelles
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:7759-7769
In this communication, we describe the synthesis and biological evaluation of tacripyrimedones 1-5, a series of new tacrine-1,4-dihydropyridine hybrids bearing the general structure of 11-amino-12-aryl-3,3-dimethyl-3,4,5,7,8,9,10,12-octahydrodibenzo[
Autor:
Mercedes Villarroya, Rafael León, José Marco-Contelles, Cristóbal de los Ríos, Antonio G. García, Manuela G. López
Publikováno v:
European Journal of Medicinal Chemistry. 43:668-674
The synthesis and pharmacology of 6-amino-1,4-dihydropyridines, such as ethyl 6-amino-4-aryl-5-cyano-1,4-dihydro-2-methyl-3-pyridinecarboxylic acids ( 3 – 16 ) and 2-amino-4-aryl-7,7-dimethyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinenitriles ( 17 –
Autor:
Beatriz Sevilla-Morán, M. Inés Santín-Montanyá, José Luis Alonso-Prados, Pilar Sandín-España, Mercedes Villarroya-Ferruz
Publikováno v:
Repositorio de Resultados de Investigación del INIA
INIA: Repositorio de Resultados de Investigación del INIA
Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria INIA
INIA: Repositorio de Resultados de Investigación del INIA
Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria INIA
When herbicides are sprayed in the field, a proportion of the herbicide falls onto leaves and soil surfaces, where it can be exposed to sunlight, generating photoproducts that can be more toxic and/or persistent than the parent substance and affect h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8279f4df5d2ecd1777cd693e2a7bbea
https://hdl.handle.net/20.500.12792/4144
https://hdl.handle.net/20.500.12792/4144
Publikováno v:
European Journal of Medicinal Chemistry. 41:1464-1469
The synthesis and biological evaluation of ethyl 5-amino-4-(3-pyridyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrano[2,3-b]quinoline-3-carboxylates (9-11) is described. We have found that these compounds inhibit AChE with a mild potency, mitigates the [Ca(2+