Publications (33)

2022

  1. Structure-activity relationships reveal a 2-furoyloxychalcone as a potent cytotoxic and apoptosis inducer for human U-937 and HL-60 leukaemia cells

    Bioorganic Chemistry, Vol. 127

  2. Guanidine Derivatives Containing the Chalcone Skeleton Are Potent Antiproliferative Compounds against Human Leukemia Cells

    International journal of molecular sciences, Vol. 23, Núm. 24

2021

  1. Synthetic efforts on the road to marine natural products bearing 4-O-2,3,4,6-tetrasubstituted THPs: an update

    RSC Advances, Vol. 11, Núm. 10, pp. 5832-5858

2020

  1. The synthetic flavanone 6-methoxy-2-(naphthalen-1-yl)chroman-4-one induces apoptosis and activation of the MAPK pathway in human U-937 leukaemia cells

    Bioorganic Chemistry, Vol. 94

2019

  1. Modular total syntheses of thymifodioic/incanic acids

    Arabian Journal of Chemistry, Vol. 12, Núm. 8, pp. 3764-3775

2018

  1. Stereoselective Synthesis of Highly Substituted Tetrahydropyrans through an Evans Aldol-Prins Strategy

    Journal of Organic Chemistry, Vol. 83, Núm. 16, pp. 9039-9066

  2. 3′-Hydroxy-3,4′-dimethoxyflavone-induced cell death in human leukaemia cells is dependent on caspases and reactive oxygen species and attenuated by the inhibition of JNK/SAPK

    Chemico-Biological Interactions, Vol. 288, pp. 1-11

2017

  1. 3′-Hydroxy-3,4′-dimethoxyflavone blocks tubulin polymerization and is a potent apoptotic inducer in human SK-MEL-1 melanoma cells

    Bioorganic and Medicinal Chemistry, Vol. 25, Núm. 21, pp. 6060-6070

2016

  1. The Evans Aldol-Prins cyclization: A general and stereoselective method for the synthesis of 2,3,4,5,6-pentasubstituted tetrahydropyrans

    Chemical Communications, Vol. 52, Núm. 16, pp. 3380-3383

  2. Gardenin B-induced cell death in human leukemia cells involves multiple caspases but is independent of the generation of reactive oxygen species

    Chemico-Biological Interactions, Vol. 256, pp. 220-227

2015

  1. Oxasqualenoids from Laurencia viridis: Combined spectroscopic-computational analysis and antifouling potential

    Journal of Natural Products, Vol. 78, Núm. 4, pp. 712-721

  2. A new iridoid, verbascoside and derivatives with inhibitory activity against Taq DNA polymerase

    Bioorganic and Medicinal Chemistry Letters, Vol. 25, Núm. 4, pp. 914-918

2014

  1. Chemistry and biological activity of coumarins at molecular level

    Natural Product Communications, Vol. 9, Núm. 8, pp. 1091-1094

2013

  1. Derivatives of grindelic acid: From a non-active natural diterpene to synthetic antitumor derivatives

    European Journal of Medicinal Chemistry, Vol. 67, pp. 28-38

2012

  1. Inhibition of Taq DNA polymerase by iridoid aglycone derivates.

    Cellular and molecular biology (Noisy-le-Grand, France), Vol. 58 Suppl

2011

  1. Mass spectrometry studies of iridoid aglycone derivatives

    Rapid Communications in Mass Spectrometry

  2. On the configuration of five-membered rings: A spin-spin coupling constant approach

    Chemistry - A European Journal, Vol. 17, Núm. 23, pp. 6338-6347

2010

  1. Enhancement of antiproliferative activity by molecular simplification of catalpol

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

  2. (E)-2-((4R,5R)-5-((benzyloxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)but-2-ene-1,4-diol

    MolBank, Vol. 2010, Núm. 2, pp. 1-4

  3. (-)-5-[(4R,5R)-5-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-4,7-dihydro-1,3-dioxepine

    MolBank, Vol. 2010, Núm. 2, pp. 1-3