Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Antonio Fernández Medarde"'
Autor:
Víctor Rodríguez Martín-Aragón, Mónica Trigal Martínez, Cristina Cuadrado, Antonio Hernández Daranas, Antonio Fernández Medarde, José M. Sánchez López
Publikováno v:
ACS Omega, Vol 8, Iss 42, Pp 39873-39885 (2023)
Externí odkaz:
https://doaj.org/article/ae4dbf88a60f4fc5beafe3a5367cd817
Autor:
Víctor Rodríguez Martín-Aragón, Francisco Romero Millán, Cristina Cuadrado, Antonio Hernández Daranas, Antonio Fernández Medarde, José M. Sánchez López
Publikováno v:
Marine Drugs, Vol 21, Iss 10, p 526 (2023)
Using the OSMAC (One Strain Many Compounds) approach, the actinobacterium Streptomyces griseorubiginosus, derived from an unidentified cnidarian collected from a reef near Pointe de Bellevue in Réunion Island (France), was subjected to cultivation u
Externí odkaz:
https://doaj.org/article/5c04c6889c4e4b3d9c1981e420bf547c
Autor:
Melissa García-Caballero, Librada Cañedo, Antonio Fernández-Medarde, Miguel Ángel Medina, Ana R. Quesada
Publikováno v:
Marine Drugs, Vol 12, Iss 1, Pp 279-299 (2014)
In the course of a screening program for the inhibitors of angiogenesis from marine sources, AD0157, a pyrrolidinedione fungal metabolite, was selected for its angiosupressive properties. AD0157 inhibited the growth of endothelial and tumor cells in
Externí odkaz:
https://doaj.org/article/e5693be9634c4b1bbbb62048ea36682d
Autor:
Antonio Fernández-Medarde, Eugenio Santos, Rósula García-Navas, Andrea Olarte-San Juan, Rocío Fuentes-Mateos, Alberto Fernández-Medarde, José María Sánchez-López
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biomolecules
Biomolecules, Vol 11, Iss 1128, p 1128 (2021)
Volume 11
Issue 8
instname
Biomolecules
Biomolecules, Vol 11, Iss 1128, p 1128 (2021)
Volume 11
Issue 8
© 2021 by the authors.
Recent breakthroughs have reignited interest in RAS GEFs as direct therapeutic targets. To search for new inhibitors of SOS GEF activity, a repository of known/approved compounds (NIH-NACTS) and a library of new marine co
Recent breakthroughs have reignited interest in RAS GEFs as direct therapeutic targets. To search for new inhibitors of SOS GEF activity, a repository of known/approved compounds (NIH-NACTS) and a library of new marine co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41513b689ed08940b57d92b7ff319c3e
http://hdl.handle.net/10261/260995
http://hdl.handle.net/10261/260995
Autor:
José María Sánchez López, Julian Davies, Omar M. El-Halfawy, Antonio Fernández Medarde, Agatha N. Jassem, David P. Speert, Miguel A. Valvano, Slade A. Loutet
Publikováno v:
Loutet, S A, El-Halfawy, O M, Jassem, A N, Sánchez López, J M, Fernández Medarde, A, Speert, D P, Davies, J E & Valvano, M A 2015, ' Identification of synergists that potentiate the action of polymyxin B against Burkholderia cenocepacia ', International Journal of Antimicrobial Agents, vol. 46, no. 4, pp. 376-380 . https://doi.org/10.1016/j.ijantimicag.2015.05.010
Burkholderia cenocepacia and other members of the Burkholderia cepacia complex (Bcc) are highly multidrug-resistant bacteria that cause severe pulmonary infections in patients with cystic fibrosis. A screen of 2686 compounds derived from marine organ
Autor:
Antonio Fernández-Medarde, Melissa García-Caballero, Ana R. Quesada, Miguel Ángel Medina, Librada Cañedo
Publikováno v:
Marine Drugs
Volume 12
Issue 1
Pages: 279-299
Marine Drugs, Vol 12, Iss 1, Pp 279-299 (2014)
Volume 12
Issue 1
Pages: 279-299
Marine Drugs, Vol 12, Iss 1, Pp 279-299 (2014)
In the course of a screening program for the inhibitors of angiogenesis from marine sources, AD0157, a pyrrolidinedione fungal metabolite, was selected for its angiosupressive properties. AD0157 inhibited the growth of endothelial and tumor cells in
Publikováno v:
Bioorganicmedicinal chemistry. 15(15)
A series of analogues of the potentially angiogenic inhibitor aeroplysinin-1 1 were synthesized and their in vitro antiangiogenic and cytotoxic activities evaluated. In the case of epoxy ketone 6 and azlactone 36 the relationship sprouting inhibition
Autor:
Alberto Fernández-Medarde, Rocío Fuentes-Mateos, Rósula García-Navas, Andrea Olarte-San Juan, José María Sánchez-López, Antonio Fernández-Medarde, Eugenio Santos
Publikováno v:
Biomolecules, Vol 11, Iss 8, p 1128 (2021)
Recent breakthroughs have reignited interest in RAS GEFs as direct therapeutic targets. To search for new inhibitors of SOS GEF activity, a repository of known/approved compounds (NIH-NACTS) and a library of new marine compounds (Biomar Microbial Tec
Externí odkaz:
https://doaj.org/article/a8fddbd778c14f529f9e0b5700da1d99