Eugenio
Uriarte Villares
Publicacións nas que colabora con Eugenio Uriarte Villares (43)
2017
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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
2013
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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
2011
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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
2007
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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
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Synthesis and anti-HIV activity of novel cyclopentenyl nucleoside analogues of 8-azapurine
Chemical and Pharmaceutical Bulletin, Vol. 54, Núm. 10, pp. 1418-1420
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Synthesis and structural study of carbocyclic analogues of 1,2-disubstituted nucleosides
Structural Chemistry, Vol. 17, Núm. 5, pp. 465-471
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Synthesis of 1,2-disubstituted carbocyclic nucleoside analogues of cytidine
Helvetica Chimica Acta, Vol. 89, Núm. 5, pp. 954-961
2005
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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
2003
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Crystal structure of {2-[4-(4-chlorophenyI)-4-hydroxy-l-piperidinyl- methyl]cyclopentyl}-(4-fluorophenyl)-methanone, C24H27CIFNO2
Zeitschrift fur Kristallographie - New Crystal Structures, Vol. 218, Núm. JG, pp. 469-470
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Crystal structure of {2-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl-methyl] cyclopentyl}-(4-fluorophenyl)-methanone, C24H27ClFNO 2
Zeitschrift fur Kristallographie - New Crystal Structures, Vol. 218, Núm. 4, pp. 437-438
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Purine derivatives of 1,2-disubstituted cyclohexane analogues of nucleosides
Nucleosides, Nucleotides and Nucleic Acids
2002
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Novel 1,2-disubstituted carbocyclic nucleoside analogues of purine with a cyclopentene ring
Synthesis, pp. 2445-2449
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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
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Synthesis, conformational analysis and antiviral and antitumoral activity of new 1,2-disubstituted carbocyclic nucleosides
European Journal of Medicinal Chemistry, Vol. 37, Núm. 9, pp. 755-760
2001
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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
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Synthesis of 1,2-disubstituted carbocyclic analogs of pyrimidine and purine nucleosides
Synthesis, pp. 1532-1538
2000
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A novel approach for the virtual screening and rational design of anticancer compounds
Journal of Medicinal Chemistry, Vol. 43, Núm. 10, pp. 1975-1985
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Design, synthesis, conformational analysis and biological activities of purine-based 1,2-di-substituted carbocyclic nucleosides
Chemical and Pharmaceutical Bulletin, Vol. 48, Núm. 2, pp. 293-295
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Synthesis of new 4-cyclohexylcoumarin derivatives
Synthesis, pp. 643-645