Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Javier Rodríguez-Salarichs"'
Autor:
Lucía Payá-Tormo, Javier Rodríguez-Salarichs, Alicia Prieto, María Jesús Martínez, Jorge Barriuso
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 7 (2019)
Some enzymes that belong to the Candida rugosa-like lipase family (abH03. 01) combine the activities of lipases and sterol esterases. Thus, they can act on water-insoluble carboxylic esters releasing long-chain fatty acids but also on sterol esters,
Externí odkaz:
https://doaj.org/article/d6179870d6a245b3a44da0f54e0fe4b3
Autor:
Hortensia Rodríguez, Julieta Coro, Anabel Lam, Esperanza Salfrán, Javier Rodríguez-Salarichs, Margarita Suárez, Fernando Albericio, Nazario Martin
Publikováno v:
ARKIVOC, Vol 2011, Iss 9, Pp 125-141 (2011)
Externí odkaz:
https://doaj.org/article/420b7d7b90c749b39142aaf6f5de3b90
Autor:
Andrea Jantsch, Lidia Nieto, Jürg Gertsch, Javier Rodríguez-Salarichs, Ruth Matesanz, Jesús Jiménez-Barbero, J. Fernando Díaz, Ángeles Canales, Karl-Heinz Altmann
Publikováno v:
Molecules, Vol 21, Iss 8, p 1010 (2016)
12-Aza-epothilones (azathilones) incorporating quinoline side chains and bearing different N12-substituents have been synthesized via highly efficient RCM-based macrocyclizations. Quinoline-based azathilones with the side chain N-atom in the meta-pos
Externí odkaz:
https://doaj.org/article/ccbbdb16c1a049729b87298363d0867f
Autor:
Javier Rodríguez-Salarichs, María Jesús Martínez, Alicia Prieto, Jorge Barriuso, Mario García de Lacoba
Publikováno v:
Journal of Chemical Information and Modeling
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
26 p.-5 fig.
Lipases are enzymes able to catalyze the hydrolysis or synthesis of triglycerides, depending on the reaction conditions, whereas sterol esterases show the same ability on sterol esters. Structurally, both kinds of enzymes display an
Lipases are enzymes able to catalyze the hydrolysis or synthesis of triglycerides, depending on the reaction conditions, whereas sterol esterases show the same ability on sterol esters. Structurally, both kinds of enzymes display an
Autor:
Jesús Jiménez-Barbero, Ángeles Canales, Katja Bargsten, María A. Oliva, Michel O. Steinmetz, Andrea E. Prota, Javier Rodríguez-Salarichs, J. Fernando Díaz, Youssef L. Bennani
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Noscapine is a natural alkaloid that is used as an antitussive medicine. However, it also acts as a weak anticancer agent in certain in vivo models through a mechanism that is largely unknown. Here, we performed structural studies and show that the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8375912e026ffea237e1cb8998d7254f
http://hdl.handle.net/10261/216841
http://hdl.handle.net/10261/216841
Autor:
Alicia Prieto, Lucía Payá-Tormo, Javier Rodríguez-Salarichs, Jorge Barriuso, María Jesús Martínez
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 7 (2019)
Some enzymes that belong to the Candida rugosa-like lipase family (abH03. 01) combine the activities of lipases and sterol esterases. Thus, they can act on water-insoluble carboxylic esters releasing long-chain fatty acids but also on sterol esters,
Autor:
Fabienne Z. Gaugaz, Jürg Gertsch, Jesús Jiménez-Barbero, Raphael Schiess, Simon Glauser, Stefan Vetterli, Ángeles Canales, José Fernando Díaz, Oliver P. Horlacher, Christian N. Kuzniewski, Mariano Redondo-Horcajo, Karl-Heinz Altmann, Javier Rodríguez-Salarichs
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
16 p.-6 fig.-2 tab.
A series of new 3‐deoxy‐C(12),C(13)‐trans‐cyclopropyl‐epothilones have been prepared, bearing benzothiazole, quinoline, thiazol‐5‐ylvinyl, or isoxazol‐3‐ylvinyl side chains. For analogs with fused aromatic s
A series of new 3‐deoxy‐C(12),C(13)‐trans‐cyclopropyl‐epothilones have been prepared, bearing benzothiazole, quinoline, thiazol‐5‐ylvinyl, or isoxazol‐3‐ylvinyl side chains. For analogs with fused aromatic s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba16ce0535aa0e652544810d306c0cce
http://hdl.handle.net/10261/181502
http://hdl.handle.net/10261/181502
Autor:
Lucía, Payá-Tormo, Javier, Rodríguez-Salarichs, Alicia, Prieto, María Jesús, Martínez, Jorge, Barriuso
Publikováno v:
Frontiers in Bioengineering and Biotechnology
Some enzymes that belong to the Candida rugosa-like lipase family (abH03. 01) combine the activities of lipases and sterol esterases. Thus, they can act on water-insoluble carboxylic esters releasing long-chain fatty acids but also on sterol esters,
Autor:
Michel Jordi, John H. Miller, J. Fernando Díaz, Benet Pera, Grégory Menchon, Juan Estévez Gallego, José Manuel Andreu, Javier Rodríguez-Salarichs, Didier Zuwerra, Andrea E. Prota, Enrique Calvo, Gonzalo Sáez-Calvo, Jessica J. Field, Karl-Heinz Altmann
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
41 p.-8 fig.-2 tab. Field, Jessica J. et al.
The marine natural product zampanolide and analogues thereof constitute a new chemotype of taxoid site microtubule-stabilizing agents with a covalent mechanism of action. Zampanolide-ligated tubulin h
The marine natural product zampanolide and analogues thereof constitute a new chemotype of taxoid site microtubule-stabilizing agents with a covalent mechanism of action. Zampanolide-ligated tubulin h
Autor:
Herbert N. Arst, Miguel A. Peñalva, J. Fernando Díaz, Areti Pantazopoulou, Víctor G. Tagua, Mario Pinar, Javier Rodríguez-Salarichs, Vivian de los Ríos
Publikováno v:
Proceedings of the National Academy of Sciences. 112:4346-4351
The oligomeric complex transport protein particle I (TRAPPI) mediates nucleotide exchange on the RAB GTPase RAB1/Ypt1. TRAPPII is composed of TRAPPI plus three additional subunits, Trs120, Trs130, and Trs65. Unclear is whether TRAPPII mediates nucleo