Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Librada Cañedo"'
Autor:
Ana Ceniceros, Librada Cañedo, Carmen Méndez, Carlos Olano, Carmen Schleissner, Carmen Cuevas, Fernando de la Calle, José A. Salas
Publikováno v:
Metabolites, Vol 13, Iss 10, p 1091 (2023)
Three novel lipopeptides, PM130391 (1), PM130392 (2), and PM140293 (3) were obtained from cultures of Streptomyces tuirus PHM034 isolated from a marine sediment. Structural elucidation of the three compounds showed they belong to the nonribosomal pep
Externí odkaz:
https://doaj.org/article/aaa2ae51a5bb42d7bd2dd8950d9374ef
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:
Raúl García-Salcedo, Rubén Álvarez-Álvarez, Carlos Olano, Librada Cañedo, Alfredo F. Braña, Carmen Méndez, Fernando de la Calle, José A. Salas
Publikováno v:
Marine Drugs, Vol 16, Iss 8, p 259 (2018)
Jomthonic acids (JAs) are a group of natural products (NPs) with adipogenic activity. Structurally, JAs are formed by a modified β-methylphenylalanine residue, whose biosynthesis involves a methyltransferase that in Streptomyces hygroscopicus has be
Externí odkaz:
https://doaj.org/article/9f015a5240174a7d865924deb7dc7bcb
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d75da067596fd826593b53c754f97a
https://doi.org/10.3390/md12010279
https://doi.org/10.3390/md12010279