Publicacións nas que colabora con Marta Teijeira Bautista (11)

2016

  1. Topological sub-structural molecular design (TOPS-MODE): a useful tool to explore key fragments of human A3adenosine receptor ligands

    Molecular Diversity, Vol. 20, Núm. 1, pp. 55-76

2010

  1. Stereoselective synthesis of novel isonucleoside analogues of purine with a tetrahydropyran ring

    Synthesis, pp. 425-430

  2. Synthesis and cytostatic activity of purine nucleosides derivatives of allofuranose

    European Journal of Medicinal Chemistry, Vol. 45, Núm. 12, pp. 6114-6119

2009

  1. Synthesis of new 9-beta-D-allofuranosyl purines as potential antitumor agents

    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY

2008

  1. New QSAR combined strategy for the design of A1 adenosine receptor agonists

    Bioorganic and Medicinal Chemistry, Vol. 16, Núm. 4, pp. 1658-1675

2005

  1. A radial distribution function approach to predict A 2B agonist effect of adenosine analogues

    Bioorganic and Medicinal Chemistry, Vol. 13, Núm. 3, pp. 601-608

  2. BCUT descriptors to predicting affinity toward A3 adenosine receptors

    Bioorganic and Medicinal Chemistry Letters, Vol. 15, Núm. 15, pp. 3491-3495

  3. Geometry, topology, and atom-weights assembly descriptors to predicting A1 adenosine receptors agonists

    Bioorganic and Medicinal Chemistry Letters, Vol. 15, Núm. 10, pp. 2641-2645

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

    Nucleosides, Nucleotides and Nucleic Acids

1999

  1. Nucleoside analogues of purine with a 1,2-disubstituted cyclopentene ring

    Nucleosides and Nucleotides