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Ortuso Francesco
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http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_10/101021jm0493461/authorship/9
http://hub.abes.fr/oup/periodical/bioinformatics/2006/volume_22/issue_12/101093bioinformaticsbtl115/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_19/101021jm0504609/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_23/101021jm040903t/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_4/101021jm011040w/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_16/101021jm800132g/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_4/101021jm060869d/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_3/101021jm060868l/authorship/9
http://hub.abes.fr/acs/periodical/jcisd8/2005/volume_45/issue_3/101021ci0496595/authorship/2
http://hub.abes.fr/acs/periodical/jnprdf/2006/volume_69/issue_6/101021np060015w/authorship/14
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GBPM: GRID-based pharmacophore model: concept and application studies to protein-protein recognition
Molecular Modeling of DNA Cross-linking Analogues Based on the Azinomycin Scaffold
DNA Cross-Linking by Azinomycin B: Monte Carlo Simulations in theEvaluation of Sequence Selectivity
Further Studies on the Interaction of the 5-Hydroxytryptamine3 (5-HT3)Receptor with Arylpiperazine Ligands. Development of a New 5-HT3 ReceptorLigand Showing Potent Acetylcholinesterase Inhibitory Properties
Quercetin as the Active Principle of Hypericum hircinum Exerts a Selective Inhibitory Activityagainst MAO-A: Extraction, Biological Analysis, and Computational Study
Monoamine Oxidase Isoform-DependentTautomeric Influence in the Recognition of3,5-Diaryl Pyrazole Inhibitors
Molecular Modeling, Synthesis, and Preliminary Biological Evaluation ofGlutathione-S-Transferase Inhibitors as Potential Therapeutic Agents
Synthesis, Molecular Modeling Studies, and Selective Inhibitory Activityagainst Monoamine Oxidase of 1-Thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazole Derivatives
Selective Inhibitory Activity against MAO and Molecular Modeling Studies of2-Thiazolylhydrazone Derivatives
Synthesis, Stereochemical Identification, and Selective Inhibitory Activity against Human Monoamine Oxidase-B of 2-Methylcyclohexylidene-(4-arylthiazol-2-yl)hydrazones
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