Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jesús Ángel de la Fuente"'
Autor:
Sonia Moliner-Cubel, Jesús Ángel de la Fuente, Maria G. Gomez-Lorenzo, Noemí Bahamontes-Rosa, Jose Luis Lavandera, Ruben Gonzalez Del Rio, María Martínez-Hoyos, Alfonso Mendoza-Losana, Carolina Ródenas, Jose F. Garcia-Bustos, Ane Rodríguez-Alejandre
Publikováno v:
International Journal for Parasitology: Drugs and Drug Resistance, Vol 8, Iss 2, Pp 295-303 (2018)
International Journal for Parasitology: Drugs and Drug Resistance
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
International Journal for Parasitology: Drugs and Drug Resistance
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Phenotypic screening has produced most of the new chemical entities currently in clinical development for malaria, plus many lead compounds active against Plasmodium falciparum asexual stages. However, lack of knowledge about the mode of action of th
Autor:
Francesc X. Ruiz, Michael Betz, Felix Terwesten, Jesús Ángel de la Fuente, Alberto Podjarny, Alexandra Cousido-Siah, Xavier Parés, Sonia Manzanaro, Sergio Porté, Gerhard Klebe, María Jesús Martín, Angel R. de Lera, Jaume Farrés, Andre Mitschler
Publikováno v:
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Aldo-keto reductases (AKRs) are mostly monomeric enzymes which fold into a highly conserved (α/β)8barrel, while their substrate specificity and inhibitor selectivity are determined by interaction with residues located in three highly variable exter
Autor:
Stephen P. Watson, Adelheid Roth, Anna Sava, Greg J. Osborne, David John Nash, Paloma Perez, Ben Powney, Corrado Corti, Magalie Rocheville, Paul W. Smith, Clive Leslie Branch, Federica Bianchi, Pier D’Alessandro, Emma Koppe, Maite de los Frailes, Jesús Ángel de la Fuente, Annarosa Ugolini, Dino Montanari, Stephen L. Garland
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:759-762
The optimisation of an HTS hit series (1) leading to the identification of structurally novel, selective, orally bioavailable mGluR2 positive modulators GSK1331258 and GSK1331268 is described. Structure-activity relationships, attenuation of dopamine
Autor:
Alberto Podjarny, Gerhard Klebe, C. Rechlin, Sergio Porté, Andre Mitschler, Xavier Parés, Alexandra Cousido-Siah, Jesús Ángel de la Fuente, Isidro Crespo, María Jesús Martín, Angel R. de Lera, Marta Domínguez, F.X. Ruiz, Jaume Farrés
Publikováno v:
ChemMedChem. 10(12)
The human enzymes aldose reductase (AR) and AKR1B10 have been thoroughly explored in terms of their roles in diabetes, inflammatory disorders, and cancer. In this study we identified two new lead compounds, 2-(3-(4-chloro-3-nitrobenzyl)-2,4-dioxo-3,4
Autor:
Jesús Ángel de la Fuente, Sonia Manzanaro, Santos Luengo, Teresa García De Quesada, Isabel Reymundo, María Jesús Martín, Federico Gago
Publikováno v:
Journal of Medicinal Chemistry. 46:5208-5221
Aldose reductase (ALR2) has been implicated in the etiology of diabetic complications, including blindness. Because of the limited number of currently available drugs for the prevention of these long-term complications, the discovery of new ALR2 inhi
Autor:
David G. Tew, Alfonso Rivera-Sagredo, Paloma Perez, Cheryl A. Janson, Nestor O. Concha, Martin Gilpin, Juan A. Hueso-Rodríguez, Michael Rees, John H. Bateson, Jesús Ángel de la Fuente, Helen F. Boyd, Niconovich Nancy, Stewart C. Pearson, Christy Cheever, David J. Payne, E. Diez, Stephen Rittenhouse
Publikováno v:
Antimicrobial Agents and Chemotherapy. 46:1880-1886
Metallo-β-lactamases provide bacteria with an efficient and effective way of mediating resistance to β-lactam-based antibacterial agents. More significantly, they confer resistance to carbapenems. Therefore, if metallo-β-lactamases increase in pre
Autor:
Librada M. Cañedo, Jesús Ángel de la Fuente, Carlos Jiménez, Ricardo Riguera, María J. Ferreiro, Cristina Gesto
Publikováno v:
Tetrahedron Letters. 40:6841-6844
Agrochelin (1), a new cytotoxic thiazole alkaloid, has been isolated from the fermentation broth of a marine unicellular bacterium belonging to genus Agrobacterium. Its structure was determined from spectral data and chemical transformations. Agroche
Autor:
Santiago Álvarez García, Alfonso Fernández Mateos, Jesús Ángel de la Fuente, Amador Menéndez, Sue S. Cross, Juan J. Marugan
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:1471-1474
Here we report a novel non-nucleoside compound, PM-92131(+), with in vitro anti-HIV-1 activity. This product was synthesized as a pure enantiomer via diastereomeric ester formation and selective crystallisation and its absolute stereochemistry was de
Autor:
María J. Ferreiro, Jesús Ángel de la Fuente, Ricardo Riguera, Carlos Jiménez, Librada M. Cañedo, Cristina Gesto
Publikováno v:
ChemInform. 30
Agrochelin (1), a new cytotoxic thiazole alkaloid, has been isolated from the fermentation broth of a marine unicellular bacterium belonging to genus Agrobacterium. Its structure was determined from spectral data and chemical transformations. Agroche
Autor:
Marta Domínguez, Jesús Ángel de la Fuente, Alberto Podjarny, Alexandra Cousido-Siah, María Jesús Martín, Angel R. de Lera, F.X. Ruiz, C. Rechlin, Jaume Farrés, Gerhard Klebe, Isidro Crespo, Andre Mitschler, Sergio Porté, Xavier Parés
Publikováno v:
ChemMedChem. 10:1941-1941