Publications in collaboration with researchers from Universidad de Salamanca (20)

2022

  1. Alciporin, a pore-forming protein as complementary defense mechanism in Millepora alcicornis

    Frontiers in Marine Science, Vol. 9

2018

  1. A Small Molecule Tubulin Depolymerizing Agent Identified by a Phenotypic Drug Discovery Approach

    Journal of Molecular and Clinical Medicine, Vol. 1, Núm. 2, pp. 67-76

  2. Correction: CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia [Oncotarget, 8 (2017) (29679-29698)] Doi: 10.18632/oncotarget.11425

    Oncotarget

2017

  1. CM363, a novel naphthoquinone derivative which acts as multikinase modulator and overcomes imatinib resistance in chronic myelogenous leukemia

    Oncotarget, Vol. 8, Núm. 18, pp. 29679-29698

2016

  1. Ring-closing metathesis as key step in the synthesis of Luffarin I, 16-epi-Luffarin I and Luffarin A

    Molecular Diversity, Vol. 20, Núm. 2, pp. 369-377

2015

  1. Biomimetic synthesis of two salmahyrtisanes: Salmahyrtisol A and hippospongide A

    Journal of Organic Chemistry, Vol. 80, Núm. 9, pp. 4566-4572

  2. Synthesis and bioactivity of Luffarin I

    Marine Drugs, Vol. 13, Núm. 4, pp. 2407-2423

  3. Synthesis of Luffarin L and 16- epi -Luffarin L Using a Temporary Silicon-Tethered Ring-Closing Metathesis Reaction

    Journal of Organic Chemistry, Vol. 80, Núm. 12, pp. 6447-6455

2014

  1. Synthesis and biological activity of polyalthenol and pentacyclindole analogues

    European Journal of Medicinal Chemistry, Vol. 73, pp. 265-279

2013

  1. Molecular docking studies of the interaction between propargylic enol ethers and human DNA topoisomerase IIα

    Bioorganic and Medicinal Chemistry Letters, Vol. 23, Núm. 19, pp. 5382-5384

2012

  1. Saiyacenols A and B: The key to solve the controversy about the configuration of aplysiols

    Tetrahedron, Vol. 68, Núm. 36, pp. 7275-7279

  2. β-Lapachone analogs with enhanced antiproliferative activity

    European Journal of Medicinal Chemistry, Vol. 53, pp. 264-274

2011

  1. A modular approach to trim cellular targets in anticancer drug discovery

    Bioorganic and Medicinal Chemistry Letters, Vol. 21, Núm. 22, pp. 6641-6645

  2. Cytotoxic oxasqualenoids from the red alga Laurencia viridis

    European Journal of Medicinal Chemistry, Vol. 46, Núm. 8, pp. 3302-3308

  3. New polyether triterpenoids from Laurencia viridis and their biological evaluation

    Marine Drugs, Vol. 9, Núm. 11, pp. 2220-2235

  4. Synthesis, biological evaluation and structural characterization of novel glycopeptide analogues of nociceptin N/OFQ

    Organic and Biomolecular Chemistry, Vol. 9, Núm. 17, pp. 6133-6142

2010

  1. Enhancement of antiproliferative activity by molecular simplification of catalpol

    Bioorganic and Medicinal Chemistry, Vol. 18, Núm. 7, pp. 2515-2523

  2. Mitotic arrest induced by a novel family of DNA topoisomerase II inhibitors

    Journal of Medicinal Chemistry, Vol. 53, Núm. 9, pp. 3835-3839

  3. Synthesis, biological and structural characterization of novel glycopeptide analogs of nociceptin

    The FASEB Journal

1990

  1. New ent-pimarane diterpenes

    Tetrahedron, Vol. 46, Núm. 6, pp. 1923-1930