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Persico Marco
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http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_6/101021jm049510k/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_24/101021jm060899g/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_23/101021jm050257d/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_4/101021jm061429p/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_11/101021jm701253t/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_5/101021jm7012375/authorship/4
http://hub.abes.fr/acs/periodical/bichaw/2005/volume_44/issue_28/101021bi047437u/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_5/101021jm701247k/authorship/7
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Design, Synthesis, and Structure-Activity Relationship Studies of 4-Quinolinyl- and 9-Acrydinylhydrazones as Potent Antimalarial Agents
Specific Targeting Highly Conserved Residues in the HIV-1 ReverseTranscriptase Primer Grip Region. Design, Synthesis, and BiologicalEvaluation of Novel, Potent, and Broad Spectrum NNRTIs with AntiviralActivity
Development of Molecular Probes for the Identification of Extra InteractionSites in the Mid-Gorge and Peripheral Sites of Butyrylcholinesterase (BuChE).Rational Design of Novel, Selective, and Highly Potent BuChE Inhibitors
Clotrimazole Scaffold as an Innovative Pharmacophore Towards Potent Antimalarial Agents: Design, Synthesis, and Biological and Structure-Activity Relationship Studies
Specific Targeting of Hepatitis C Virus NS3 RNA Helicase. Discovery of thePotent and Selective Competitive Nucleotide-Mimicking Inhibitor QU663
Design and Synthesis of Potent AntimalarialAgents Based on Clotrimazole Scaffold: Exploring an Innovative Pharmacophore
Exploiting Protein Fluctuations at the Active-Site Gorge of Human Cholinesterases: Further Optimization of the Design Strategy to Develop Extremely Potent Inhibitors
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