Publicacións en colaboración con investigadores/as de Universidade de Vigo (36)

2017

  1. Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

    European Journal of Medicinal Chemistry, Vol. 139, pp. 1-11

2015

  1. Integrated Ugi-Based Assembly of Functionally, Skeletally, and Stereochemically Diverse 1,4-Benzodiazepin-2-ones

    Journal of Organic Chemistry, Vol. 80, Núm. 3, pp. 1533-1549

2013

  1. (1S,2S,5S)-2-Methyl-3-oxo-5-(prop-1-en-2-yl)cyclohexane-1-carbonitrile

    Acta Crystallographica Section E: Structure Reports Online, Vol. 69, Núm. 5

  2. Classifier ensemble based on feature selection and diversity measures for predicting the affinity of A2B adenosine receptor antagonists

    Journal of Chemical Information and Modeling, Vol. 53, Núm. 12, pp. 3140-3155

  3. Furan-2-yl]methyl acetate

    Acta Crystallographica Section E: Structure Reports Online, Vol. 69, Núm. 5

2011

  1. Synthesis and study of a series of 3-arylcoumarins as potent and selective monoamine oxidase B inhibitors

    Journal of Medicinal Chemistry, Vol. 54, Núm. 20, pp. 7127-7137

2010

  1. New approaches to 6-oxoisoaporphine and tetrahydroisoquinoline derivatives

    Helvetica Chimica Acta, Vol. 93, Núm. 7, pp. 1385-1394

2009

  1. QSAR and complex network study of the chiral HMGR inhibitor structural diversity

    Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 1, pp. 165-175

2007

  1. ANN-QSAR model for selection of anticancer leads from structurally heterogeneous series of compounds

    European Journal of Medicinal Chemistry, Vol. 42, Núm. 5, pp. 580-585

2006

  1. 3D comparative structural study of 6-hydroxy-4-methyl-5,7-dinitrocoumarin using experimental and theoretical approaches

    Structural Chemistry, Vol. 17, Núm. 5, pp. 459-464

  2. Synthesis and anti-HIV activity of novel cyclopentenyl nucleoside analogues of 8-azapurine

    Chemical and Pharmaceutical Bulletin, Vol. 54, Núm. 10, pp. 1418-1420

  3. Synthesis of 1,2-disubstituted carbocyclic nucleoside analogues of cytidine

    Helvetica Chimica Acta, Vol. 89, Núm. 5, pp. 954-961

2005

  1. 1,2-Disubstituted cyclohexane nucleosides: Comparative study for the synthesis of cis and trans adenosine analogues

    Tetrahedron, Vol. 61, Núm. 2, pp. 473-478

2004

  1. A short and convenient synthesis of new 1,2-disubstituted carbocyclic nucleoside analogues of pyrimidine based on a cyclopentene ring

    Synthesis, pp. 543-548

2003

  1. Purine derivatives of 1,2-disubstituted cyclohexane analogues of nucleosides

    Nucleosides, Nucleotides and Nucleic Acids

  2. Synthesis of carbocyclic analogues of MECA and NECA 1,2-disubstituted as potential adenosine receptor agonists

    Nucleosides, Nucleotides and Nucleic Acids

2002

  1. Novel 1,2-disubstituted carbocyclic nucleoside analogues of purine with a cyclopentene ring

    Synthesis, pp. 2445-2449

  2. Synthesis and structure-activity relationships of new arylpiperazines: Para substitution with electron-withdrawing groups decrease binding to 5-HT1A and D2A receptors

    European Journal of Medicinal Chemistry, Vol. 37, Núm. 6, pp. 503-510

  3. Synthesis of angular pyrrolocoumarins

    Synthesis, pp. 475-478

2001

  1. Resolution of racemic mixtures of carbocyclic analogues of nucleosides and assignment of their absolute configuration

    Nucleosides, Nucleotides and Nucleic Acids, Vol. 20, Núm. 4-7, pp. 1359-1361