Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Francisco Franco-Montalban"'
Autor:
Olga Cruz-López, Carolin Temps, Beatrice Longo, Samuel H. Myers, Francisco Franco-Montalban, Asier Unciti-Broceta
Publikováno v:
ACS Omega, Vol 4, Iss 25, Pp 21620-21626 (2019)
Externí odkaz:
https://doaj.org/article/d7bbf83a83494db8926d31a365016aef
Autor:
Stefano Tomassi, Francisco Franco Montalban, Rosita Russo, Ettore Novellino, Anna Messere, Salvatore Di Maro
Publikováno v:
Symmetry, Vol 11, Iss 4, p 567 (2019)
Nucleopeptides represent an intriguing class of nucleic acid analogues, in which nucleobases are placed in a peptide structure. The incorporation of D- and/or L-amino acids in nucleopeptide molecules allows the investigation of the role of backbone s
Externí odkaz:
https://doaj.org/article/262a4a3cae1546ef8e2f877ea461fd47
Autor:
Yudibeth Sixto-López, Margarita López-Viota, Sonia Panadero-Fajardo, Mavys Tabraue-Chávez, Mónica Díaz-Gavilán, José Pérez del Palacio, José Correa-Basurto, Joaquina Martín-Sánchez, Mercedes de la Cruz, Fernando Alves de Lima Franco, Nuria de Pedro, José F. Domínguez-Seglar, Victoriano Corpas-López, Francisco Franco-Montalban, Francisco Morillas-Márquez, Julian Lopez-Viota, José A. Gómez-Vidal
Publikováno v:
Journal of Medicinal Chemistry. 63:5734-5751
Leishmania (L.) infantum causes visceral, cutaneous, and mucosal leishmaniasis in humans and canine leishmaniasis in dogs. Herein, we describe that O-alkyl hydroxamate derivatives displayed potent and selective in vitro activity against the amastigot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30f935cdb8a5edc65d3b64ce1744a278
https://doi.org/10.1021/acs.jmedchem.9b02016
https://doi.org/10.1021/acs.jmedchem.9b02016
Autor:
M. Dora Carrión, Belén Rubio-Ruiz, Francisco Franco-Montalban, Pasquale Amoia, Maria Chiara Zuccarini, Chiara De Simone, M. Encarnación Camacho, Rosa Amoroso, Cristina Maccallini
Publikováno v:
European Journal of Medicinal Chemistry. 248:115112
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcdf4cc6cef4ce2288c4d903c5745209
https://doi.org/10.1016/j.ejmech.2023.115112
https://doi.org/10.1016/j.ejmech.2023.115112
Autor:
Carolin Temps, Beatrice Longo, Francisco Franco-Montalban, Olga Cruz-López, Asier Unciti-Broceta, Samuel H. Myers
Publikováno v:
ACS Omega, Vol 4, Iss 25, Pp 21620-21626 (2019)
López-Cruz, O, Temps, C, Longo, B, Myers, S, Franco-Montalban, F & Unciti-Broceta, A 2019, ' Synthesis and characterization of a click-assembled 18-atom macrocycle that displays selective AXL kinase inhibitory activity ', ACS Omega . https://doi.org/10.1021/acsomega.9b03525
ACS Omega
Digibug. Repositorio Institucional de la Universidad de Granada
instname
López-Cruz, O, Temps, C, Longo, B, Myers, S, Franco-Montalban, F & Unciti-Broceta, A 2019, ' Synthesis and characterization of a click-assembled 18-atom macrocycle that displays selective AXL kinase inhibitory activity ', ACS Omega . https://doi.org/10.1021/acsomega.9b03525
ACS Omega
Digibug. Repositorio Institucional de la Universidad de Granada
instname
A novel macrocyclic construct consisting of a pyrazolopyrimidine scaffold concatenated to a benzene ring through two triazoles has been developed to investigate uncharted chemical space with bioactive potential. The 18-atom macrocycle was assembled v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad2f698916971cc72e3c1f8404818bd
https://doaj.org/article/d7bbf83a83494db8926d31a365016aef
https://doaj.org/article/d7bbf83a83494db8926d31a365016aef
Autor:
Modesto T. López-López, Cristina Gila-Vilchez, Francisco Conejero-Lara, Juan A. Tamayo, Juan M. Cuerva, Luis Álvarez de Cienfuegos, Angel Orte, Francisco Franco-Montalban, Juan A. González-Vera, Mari C. Mañas-Torres
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
Consorcio Madroño
Consorcio Madroño
This study was supported by project PID2020-118498GB-I00 funded by MCIN/AEI/10.13039/501100011033, Spain and by project CTQ2017-85658-R funded by MCIN/AEI/10.13039/501100011033/FEDER "Una manera de hacer Europa", Spain, and by FEDER/Junta de Andaluci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::501b6e2203fd138642a9cea9a5d32baa
http://hdl.handle.net/10481/72224
http://hdl.handle.net/10481/72224
Publikováno v:
Magnetic Resonance in Chemistry. 58:118-125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8260fbd9d691777778c1bc9144d58c5
https://doi.org/10.1002/mrc.4942
https://doi.org/10.1002/mrc.4942
Autor:
Margarita López-Viota, Francisco Morillas-Márquez, Victoriano Corpas-López, Joaquina Martín-Sánchez, José Pérez del Palacio, Nuria de Pedro, Efres Belmonte-Reche, José A. Gómez-Vidal, Julián López-Viota, Mónica Díaz-Gavilán, Gemma Merino-Espinosa, Francisco Franco-Montalban
Publikováno v:
Pharmacological Research. 139:375-383
There is currently no satisfactory treatment for visceral leishmaniasis; the disease is thus in desperate need of novel drugs. The ideal candidate should be effective, safe, affordable, and administered via the oral route. Histone deacetylases (HDACs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dd67def1d6da6f2d29906c6f0146799
https://doi.org/10.1016/j.phrs.2018.11.039
https://doi.org/10.1016/j.phrs.2018.11.039
Autor:
Fabio Arias, Francisco Franco-Montalban, Miguel Romero, Juan Duarte, M. Dora Carrión, M. Encarnación Camacho
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
The selective inhibition of inducible nitric oxide synthase (iNOS) has become an interesting goal for the treatment of diseases where the immune and inflammatory response of the organism is involved. Septic shock is one prominent example of this type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45941375eda0b915e09da4bd77cfe001
https://doi.org/10.1016/j.bioorg.2022.105637
https://doi.org/10.1016/j.bioorg.2022.105637
Autor:
M. Dora Carrión, Miguel Romero, Francisco Franco-Montalban, M. Encarnación Camacho, Fabio Arias
Publikováno v:
Bioorganic & Medicinal Chemistry. 44:116294
In search of new Nitric Oxide Synthase (NOS) inhibitor agents, two isosteric series of derivatives with an imidamide scaffold (one of them with a hydroxyl group and the other with a carbonyl one) were synthesized and evaluated on inducible (iNOS) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe62c445ecd2c36d4b9e889aa676bf0
https://doi.org/10.1016/j.bmc.2021.116294
https://doi.org/10.1016/j.bmc.2021.116294