Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Eva, Falomir"'
Solanum lycopersicum heme-binding protein 2 as a potent antimicrobial weapon against plant pathogens
Autor:
Atefeh Farvardin, Eugenio Llorens, Luisa Liu-Xu, Lorena Sánchez-Giménez, Aloysius Wong, Elena G. Biosca, José M. Pedra, Eva Falomir, Gemma Camañes, Loredana Scalschi, Begonya Vicedo
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract The rise in antibiotic-resistant bacteria caused by the excessive use of antibiotics has led to the urgent exploration of alternative antimicrobial solutions. Among these alternatives, antimicrobial proteins, and peptides (Apps) have garnere
Externí odkaz:
https://doaj.org/article/453f8d96538e477cb6a8af6adb8a21c5
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Pharmaceuticals, Vol 16, Iss 6, p 808 (2023)
This work focuses on the development of thirteen benzylethylenearyl ureas and one carbamate. After the synthesis and purification of the compounds, we studied their antiproliferative action on cell lines, such as HEK-293, and cancer ones, such as HT-
Externí odkaz:
https://doaj.org/article/6beb3fcad32c4de2b6714e4f05aa213d
Autor:
Özbek, Nagihan, Vilarrocha, Eugenio Llorens, Jover, Begonya Vicedo, Ventura, Eva Falomir, Escuder, Beatriu
Publikováno v:
RSC Advances; 2024, Vol. 14 Issue 21, p15120-15128, 9p
Autor:
Lucía Pérez-Regidor, Joan Guzmán-Caldentey, Nils Oberhauser, Carmen Punzón, Balázs Balogh, José R. Pedro, Eva Falomir, Alessandra Nurisso, Péter Mátyus, J. Carlos Menéndez, Belén de Andrés, Manuel Fresno, Sonsoles Martín-Santamaría
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2326 (2022)
The innate immunity toll-like receptor 4 (TLR4) system is a receptor of paramount importance as a therapeutic target. Virtual screening following a “computer-aided drug repurposing” approach was applied to the discovery of novel TLR4 modulators w
Externí odkaz:
https://doaj.org/article/0f1178007a05470795f7fc9e89be0e3d
Autor:
Carlos Doñate-Buendia, Rafael Torres-Mendieta, Alexander Pyatenko, Eva Falomir, Mercedes Fernández-Alonso, Gladys Mínguez-Vega
Publikováno v:
ACS Omega, Vol 3, Iss 3, Pp 2735-2742 (2018)
Externí odkaz:
https://doaj.org/article/7a66b6e8bc2a4ce5a6ec6bcc90ff7931
Thirteen benzylethylenearyl ureas and one carbamate have been designed, synthesized and biologically evaluated as regards their antiproliferative activity on tumor cell lines HEK-293 and A-549 and on the immune and endothelial Jurkat T cells and HMEC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c5c79da0adadcee510b88e38ddb0ae5
https://doi.org/10.20944/preprints202304.0920.v1
https://doi.org/10.20944/preprints202304.0920.v1
Autor:
Celia Martín-Beltrán, Raquel Gil-Edo, Germán Hernández-Ribelles, Raül Agut, Pilar Marí-Mezquita, Miguel Carda, Eva Falomir
Publikováno v:
Pharmaceuticals, Vol 14, Iss 4, p 337 (2021)
Twenty-one styryl and phenethyl aryl ureas have been synthetized and biologically evaluated as multitarget inhibitors of Vascular endothelial growth factor receptor-2 VEGFR-2 and programmed death-ligand-1 (PD-L1) proteins in order to overcome resista
Externí odkaz:
https://doaj.org/article/233148e4f2004a3d8da20efd35ae8e68
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2614
Volume 24
Issue 3
Pages: 2614
Fourteen triazole-scaffold derivatives were synthetized and biologically evaluated as potential oncoimmunomodultator agents by targeting both PD-L1 and c-Myc. First, the antiproliferative activity of these molecules on the monocultures of several tum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a51301712d7c9a1d2c71b66ab8a7948
Autor:
Adriana Valls, Jose J. Andreu, Eva Falomir, Santiago V. Luis, Elena Atrián-Blasco, Scott G. Mitchell, Belén Altava
Publikováno v:
Pharmaceuticals, Vol 13, Iss 12, p 482 (2020)
The antibacterial activity of imidazole and imidazolium salts is highly dependent upon their lipophilicity, which can be tuned through the introduction of different hydrophobic substituents on the nitrogen atoms of the imidazole or imidazolium ring o
Externí odkaz:
https://doaj.org/article/4f0e884c6c7b4c42b4eba731c7ba4afc