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Journal of Natural Products|February 24, 2017
Streptenols F-I Isolated from the Marine-Derived Streptomyces misionensis BAT-10-03-023Guillermo Tarazona, Carmen Schleissner, Pilar Rodríguez, et al.
Journal of Medicinal Chemistry|February 3, 2006
Synthesis and cytotoxic evaluation of new derivatives of the marine alkaloid variolin BPilar M Fresneda, Santiago Delgado, Andrés Francesch, et al.
Health & Place|May 31, 2022
Temporal trends in within-city inequities in COVID-19 incidence rate by area-level deprivation in Madrid, SpainPedro Gullón, Daniel Cuesta-Lozano, Carmen Cuevas-Castillo, et al.
Bioconjugate Chemistry|May 29, 2009
Lamellarin D bioconjugates I: Synthesis and cellular internalization of PEG-derivativesDaniel Pla, Andrés Francesch, Pilar Calvo, et al.
Journal of Medicinal Chemistry|October 16, 2009
Total synthesis and antiproliferative activity screening of (+/-)-aplicyanins A, B and E and related analoguesMiroslav Sísa, Daniel Pla, Marta Altuna, et al.
Journal of Medicinal Chemistry|December 12, 2003
Constrained derivatives of stylostatin 1. 1. Synthesis and biological evaluation as potential anticancer agentsPilar Forns, Jordi Piró, Carmen Cuevas, et al.
ACS Omega|July 20, 2018
On the Mechanism of Action of Dragmacidins I and J, Two New Representatives of a New Class of Protein Phosphatase 1 and 2A InhibitorsPatricia G Cruz, Juan Fernando Martínez Leal, Antonio Hernández Daranas, et al.
Cancer Letters|April 6, 2005
Lamellarin D: a novel pro-apoptotic agent from marine origin insensitive to P-glycoprotein-mediated drug effluxMarie Vanhuyse, Jérôme Kluza, Christèle Tardy, et al.
Journal of Natural Products|February 3, 2018
Can Stereoclusters Separated by Two Methylene Groups Be Related by DFT Studies? The Case of the Cytotoxic Meroditerpenes HalioxepinesGuillermo Tarazona, Gonzalo Benedit, Rogelio Fernández, et al.
Organic Letters|February 3, 2007
Synthesis of IB-01211, a cyclic peptide containing 2,4-concatenated thia- and oxazoles, via Hantzsch macrocyclizationDelia Hernández, Gemma Vilar, Estela Riego, et al.
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