Publicaciones en colaboración con investigadores/as de University of Ferrara (81)

2021

  1. FATTY ACID PROFILE AND ANTIOXIDANT CAPACITY OF ORYZA sativa L. (JAPONICA SUBSPECIES) MARKETED IN ITALY AND BRAZIL: A COMPARISON

    Journal of Microbiology, Biotechnology and Food Sciences, Vol. 11, Núm. 1, pp. 1-6

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2019

  1. Design, Synthesis, and Biological Evaluation of 6-Substituted Thieno[3,2- d]pyrimidine Analogues as Dual Epidermal Growth Factor Receptor Kinase and Microtubule Inhibitors

    Journal of Medicinal Chemistry, Vol. 62, Núm. 3, pp. 1274-1290

  2. Design, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors

    European Journal of Medicinal Chemistry, Vol. 181

2018

  1. 2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition

    European Journal of Medicinal Chemistry, Vol. 143, pp. 683-698

  2. Looking at new ligands for chelation therapy

    New Journal of Chemistry, Vol. 42, Núm. 10, pp. 8021-8034

  3. Synthesis and biological evaluation of alpha-bromoacryloylamido indolyl pyridinyl propenones as potent apoptotic inducers in human leukaemia cells

    Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 33, Núm. 1, pp. 727-742

2017

  1. Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents

    European Journal of Medicinal Chemistry, Vol. 134, pp. 258-270

  2. Gender differences in the effects of cardiovascular drugs

    European Heart Journal - Cardiovascular Pharmacotherapy, Vol. 3, Núm. 3, pp. 163-182

  3. Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents

    Scientific Reports, Vol. 7

  4. Trends in net survival from liver cancer in six European Latin countries: Results from the SUDCAN population-based study

    European Journal of Cancer Prevention, Vol. 26, Núm. Trends in cancer net survival in six European Latin Countries: the SUDCAN study, pp. S56-S62

2016

  1. A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort

    Clinical Cancer Research, Vol. 22, Núm. 18, pp. 4664-4675

  2. Design and synthesis of potent in vitro and in vivo anticancer agents based on 1-(3',4',5'-trimethoxyphenyl)-2-Aryl-1H-imidazole

    Scientific Reports, Vol. 6

  3. Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation

    European Journal of Medicinal Chemistry, Vol. 108, pp. 39-52

2015

  1. Design, Synthesis, in Vitro, and in Vivo Anticancer and Antiangiogenic Activity of Novel 3-Arylaminobenzofuran Derivatives Targeting the Colchicine Site on Tubulin

    Journal of Medicinal Chemistry, Vol. 58, Núm. 7, pp. 3209-3222

  2. Synthesis and biological evaluation of a new series of 2-amino-3-aroyl thiophene derivatives as agonist allosteric modulators of the A1 adenosine receptor. A position-dependent effect study

    European Journal of Medicinal Chemistry, Vol. 101, pp. 185-204

2014

  1. Design, synthesis and biological evaluation of 3,5-disubstituted 2-amino thiophene derivatives as a novel class of antitumor agents

    Bioorganic and Medicinal Chemistry, Vol. 22, Núm. 18, pp. 5097-5109

  2. Design, synthesis and biological evaluation of arylcinnamide hybrid derivatives as novel anticancer agents

    European Journal of Medicinal Chemistry, Vol. 81, pp. 394-407

  3. HPLC Method and Antioxidant Activity for Bioactive Component Determination of Lycopersicon esculentum Mill. Varieties from a Coastal Area of Southern Spain

    Food Analytical Methods, Vol. 7, Núm. 3, pp. 660-668

  4. Synthesis and biological evaluation of novel 2-amino-3-aroyl-4-neopentyl-5- substituted thiophene derivatives as allosteric enhancers of the A1 adenosine receptor

    Bioorganic and Medicinal Chemistry, Vol. 22, Núm. 1, pp. 148-166