PEDRO
BESADA PEREIRA
TITULAR DE UNIVERSIDADE - TEMPO COMPLETO
MARTA
TEIJEIRA BAUTISTA
TITULAR DE UNIVERSIDADE - TEMPO COMPLETO
Publicacións nas que colabora con MARTA TEIJEIRA BAUTISTA (11)
2016
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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
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Stereoselective synthesis of novel isonucleoside analogues of purine with a tetrahydropyran ring
Synthesis, pp. 425-430
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Synthesis and cytostatic activity of purine nucleosides derivatives of allofuranose
European Journal of Medicinal Chemistry, Vol. 45, Núm. 12, pp. 6114-6119
2009
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Synthesis of new 9-beta-D-allofuranosyl purines as potential antitumor agents
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
2008
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New QSAR combined strategy for the design of A1 adenosine receptor agonists
Bioorganic and Medicinal Chemistry, Vol. 16, Núm. 4, pp. 1658-1675
2005
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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
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BCUT descriptors to predicting affinity toward A3 adenosine receptors
Bioorganic and Medicinal Chemistry Letters, Vol. 15, Núm. 15, pp. 3491-3495
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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
2003
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Synthesis of carbocyclic analogues of MECA and NECA 1,2-disubstituted as potential adenosine receptor agonists
Nucleosides, Nucleotides and Nucleic Acids
1999
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Nucleoside analogues of purine with a 1,2-disubstituted cyclopentene ring
Nucleosides and Nucleotides