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http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_11/101021jm001096a/authorship/7
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_16/101021jo010137n/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_24/101021jm0497545/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_22/101021jm050256l/authorship/8
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_33/101021ja061155v/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_23/101021jm0504860/authorship/7
http://hub.abes.fr/acs/periodical/bichaw/2003/volume_42/issue_45/101021bi0353629/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_4/101021jm001079l/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_5/101021jm7009292/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_14/101021jm9601359/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_24/101021jm010268g/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_14/101021jm990946n/authorship/8
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5-Substituted Tetrazoles as Bioisosteres of Carboxylic Acids. Bioisosterism andMechanistic Studies on Glutathione Reductase Inhibitors as Antimalarials
Antiplasmodial Activity and Cytotoxicity of Bis-, Tris-, and Tetraquinolineswith Linear or Cyclic Amino Linkers
Bromination Studies of the2,3-Dimethylnaphthazarin Core AllowingEasy Access to Naphthazarin Derivatives
A Fluoro Analogue of the Menadione Derivative6-[2‘-(3‘-Methyl)-1‘,4‘-naphthoquinolyl]hexanoic Acid Is aSuicide Substrate of Glutathione Reductase. Crystal Structureof the Alkylated Human Enzyme
Antimalarial, Antitrypanosomal, and Antileishmanial Activities andCytotoxicity of Bis(9-amino-6-chloro-2-methoxyacridines): Influence of theLinker
New Steroidal Diazo Ketones as Potential Photoaffinity Labeling Reagents forthe Mineralocorticoid Receptor: Synthesis and Biological Activities
2- and 3-Substituted 1,4-Naphthoquinone Derivatives as Subversive Substratesof Trypanothione Reductase and Lipoamide Dehydrogenase from Trypanosomacruzi: Synthesis and Correlation between Redox Cycling Activities and in VitroCytotoxicity
Irreversible Inactivation of Trypanothione Reductase by Unsaturated MannichBases: A Divinyl Ketone as Key Intermediate
Antimalarial Dual Drugs Based on Potent Inhibitors of Glutathione Reductase from Plasmodium falciparum
Mechanism-Based Inactivation of Thioredoxin Reductase from Plasmodiumfalciparum by Mannich Bases. Implication for Cytotoxicity
A Prodrug Form of a Plasmodium falciparum Glutathione Reductase InhibitorConjugated with a 4-Anilinoquinoline
Synthesis of 5-Nitro-2-furancarbohydrazides and Theircis-Diamminedichloroplatinum Complexes as Bitopic and Irreversible HumanThioredoxin Reductase Inhibitors
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