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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_26/m/print http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_26/m/web
Date Copyrighted	2003
Rights	Copyright © 2003 American Chemical Society
issue	26
Rights Holder	American Chemical Society
is Is Part Of of	Investigation of Neuraminidase-Substrate Recognition Using MolecularDynamics and Free Energy Calculations Novel sst4-Selective Somatostatin (SRIF) Agonists. 1. Lead Identification Usinga Betide Scan Novel sst4-Selective Somatostatin (SRIF) Agonists. 2. Analogues withβ-Methyl-3-(2-naphthyl)alanine Substitutions at Position 8 Optimization of the Pharmacophore Model for 5-HT7R Antagonism. Design andSynthesis of New Naphtholactam and Naphthosultam Derivatives Synthesis and Structure−Activity Relationship of Aminobenzophenones. ANovel Class of p38 MAP Kinase Inhibitors with High Antiinflammatory Activity Rational Design of an Indolebutanoic Acid Derivative as a Novel AldoseReductase Inhibitor Based on Docking and 3D QSAR Studies ofPhenethylamine Derivatives Structure-Based Design, Synthesis, and Antimicrobial Activity ofIndazole-Derived SAH/MTA Nucleosidase Inhibitors 2-Arylureidobenzoic Acids: Selective Noncompetitive Antagonists for theHomomeric Kainate Receptor Subtype GluR5 Parallel Solid-Phase Synthesis and Evaluation of Inhibitors of Streptomycescoelicolor Type II Dehydroquinase Synthesis and Biological Evaluation of Iodinated and Fluorinated9-(2-Hydroxypropyl) and 9-(2-Hydroxyethoxy)methyl Purine NucleosideAnalogues Improving Structure-Based Virtual Screening by Multivariate Analysis ofScoring Data Bisintercalating Threading Diacridines: Relationships between DNA Binding,Cytotoxicity, and Cell Cycle Arrest Generation of Bis-Cationic Heterocyclic Inhibitors of Bacillus subtilis HPrKinase/Phosphatase from a Ditopic Dynamic Combinatorial Library Enantioselective Responses to aPhosphorothioate Analogue ofLysophosphatidic Acid with LPA3Receptor-Selective Agonist Activity Design, Synthesis, and Biological Evaluation of IndenoisoquinolineTopoisomerase I Inhibitors Featuring Polyamine Side Chains on the LactamNitrogen Synthesis, in Vitro Affinity, and Efficacyof a Bis 8-Ethynyl-4H-imidazo[1,5a]-[1,4]benzodiazepine Analogue, the FirstBivalent α5 Subtype Selective BzR/GABAA Antagonist Novel sst4-Selective Somatostatin (SRIF) Agonists. 4. Three-DimensionalConsensus Structure by NMR Analyses of Activity for Factor Xa Inhibitors Based on Monte Carlo Simulations Computer Modeling of Selective Regions in the Active Site of Nitric OxideSynthases: Implication for the Design of Isoform-Selective Inhibitors Synthesis and Pharmacological Identification of Neutral Histamine H1-ReceptorAntagonists Constrained Derivatives of Stylostatin 1. 1. Synthesis and Biological Evaluationas Potential Anticancer Agents Systematic Surface Scan of the MostFavorable Interaction Sites ofMagnesium Ions with Tetracycline Novel Lavendamycin Analogues as Potent HIV-Reverse TranscriptaseInhibitors: Synthesis and Evaluation of Anti-Reverse Transcriptase Activity ofAmide and Ester Analogues of Lavendamycin Synthesis and Structure−Activity Relationship of Mannose-BasedPeptidomimetics Selectively Blocking Integrin α4β7 Binding to MucosalAddressin Cell Adhesion Molecule-1 Synthesis and Biological Evaluation of3-(4-Substituted-phenyl)-N-hydroxy-2-propenamides, a New Class of HistoneDeacetylase Inhibitors Design and Synthesis of Novel Bioactive Peptides and Peptidomimetics Three-Dimensional Quantitative Structure−Activity Relationship Analyses ofPeptide Substrates of the Mammalian H+/Peptide Cotransporter PEPT1 Shape Signatures: A New Approach to Computer-Aided Ligand- andReceptor-Based Drug Design Novel sst4-Selective Somatostatin (SRIF) Agonists. 3. Analogues Amenable toRadiolabeling

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