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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_6/m/print http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_6/m/web
Date Copyrighted	2004
Rights	Copyright © 2004 American Chemical Society
issue	6
Rights Holder	American Chemical Society
is Is Part Of of	Structure−Activity Relationships of Potent, Selective Inhibitors of NeuronalNitric Oxide Synthase Based on the 6-Phenyl-2-aminopyridine Structure New Analogues of Amonafide and Elinafide, Containing Aromatic Heterocycles: Synthesis, Antitumor Activity, Molecular Modeling, and DNA BindingProperties First Reported Nonpeptide AT1 Receptor Agonist (L-162,313) Acts as an AT2Receptor Agonist in Vivo Structure-Based Optimization of Novel Azepane Derivatives as PKB Inhibitors A Non-Peptide NK1 Receptor AgonistShowing Subpicomolar Affinity Evaluation of Potent and SelectiveSmall-Molecule Antagonists for theCXCR2 Chemokine Receptor New Steroidal Dimers with Antifungal and Antiproliferative Activity Design, Synthesis, and Evaluation of Novel Thienopyrrolizinones as AntitubulinAgents Selective Optimization of Side Activities: Another Way for Drug Discovery Synthesis and Evaluation of Dihydropyrroloquinolines That SelectivelyAntagonize P-Glycoprotein Anticonvulsant Activity of Phenylmethylenehydantoins: A Structure−ActivityRelationship Study Identification of Opioid Ligands Possessing Mixed μ Agonist/δ AntagonistActivity among Pyridomorphinans Derived from Naloxone, Oxymorphone, andHydropmorphone Arecoline Tripeptide Inhibitors of Proteasome Orally Active Antimalarials: Hydrolytically Stable Derivatives of10-Trifluoromethyl Anhydrodihydroartemisinin 3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a New Class ofSynthetic Histone Deacetylase Inhibitors. 3. Discovery of Novel LeadCompounds through Structure-Based Drug Design and Docking Studies, De Novo Design, Synthesis, and Pharmacology of α-Melanocyte StimulatingHormone Analogues Derived from Somatostatin by a Hybrid Approach 3-(4-Phenoxyphenyl)pyrazoles: A Novel Class of Sodium Channel Blockers Studies on Pyrrolopyrimidines as Selective Inhibitors of Multidrug-Resistance-Associated Protein in Multidrug Resistance Synthesis of a Potent Transition-StateInhibitor of5‘-Deoxy-5‘-methylthioadenosinePhosphorylase New Antibacterial Agents Derived from the DNA Gyrase InhibitorCyclothialidine Crystal Structures of Staphylococcusaureus Methionine AminopeptidaseComplexed with Keto Heterocycle andAminoketone Inhibitors Reveal theFormation of a Tetrahedral Intermediate Design, Synthesis, and Evaluation of Aza-Peptide Epoxides as Selective andPotent Inhibitors of Caspases-1, -3, -6, and -8 A Computational Model for Anthracycline Binding to DNA: TuningGroove-Binding Intercalators for Specific Sequences Comparative in Vivo Stability of Copper-64-Labeled Cross-Bridged andConventional Tetraazamacrocyclic Complexes New 2,4-Diamino-5-(2‘,5‘-substituted benzyl)pyrimidines as Potential Drugsagainst Opportunistic Infections of AIDS and Other Immune Disorders.Synthesis and Species-Dependent Antifolate Activity Design, Synthesis, and Biological Evaluation of New 8-Heterocyclic XanthineDerivatives as Highly Potent and Selective Human A2B Adenosine ReceptorAntagonists Design and Synthesis of New Templates Derived from Pyrrolopyrimidine asSelective Multidrug-Resistance-Associated Protein Inhibitors inMultidrug Resistance

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