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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_7/m/web http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_7/m/print
Date Copyrighted	1999
Rights	Copyright © 1999 American Chemical Society
issue	7
Rights Holder	American Chemical Society
is Is Part Of of	Orally Active Isoxazoline Glycoprotein IIb/IIIa Antagonists with ExtendedDuration of Action Synthesis and Anti-HIV and Anti-HBV Activities of 2‘-Fluoro-2‘,3‘-unsaturatedl-Nucleosides 1-Arylnaphthalene Lignan: A Novel Scaffold for Type 5 PhosphodiesteraseInhibitor Characterization of the Binding Site of the Histamine H3 Receptor. 1. VariousApproaches to the Synthesis of 2-(1H-Imidazol-4-yl)cyclopropylamine andHistaminergic Activity of (1R,2R)- and (1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine Quinuclidine Inhibitors of 2,3-Oxidosqualene Cyclase-Lanosterol Synthase: Optimization from Lipid Profiles Synthesis, Structure−Activity Relationships, and in Vivo Evaluations ofSubstituted Di-tert-butylphenols as a Novel Class of Potent, Selective, andOrally Active Cyclooxygenase-2 Inhibitors. 2. 1,3,4- and 1,2,4-Thiadiazole Series Synthesis and Biological Evaluation of Boron-Containing Polyamines asPotential Agents for Neutron Capture Therapy of Brain Tumors Novel Potential Agents for Human Cytomegalovirus Infection: Synthesis andAntiviral Activity Evaluation of Benzothiadiazine Dioxide Acyclonucleosides Design and Synthesis of a Potent Cyclic Analogue of the Myelin Basic ProteinEpitope MBP72-85: Importance of the Ala81 Carboxyl Group and of a CyclicConformation for Induction of Experimental Allergic Encephalomyelitis Fluorescent Pseudo-Peptide Linear Vasopressin Antagonists: Design,Synthesis, and Applications, Binding Preferences of Hydroxamate Inhibitors of the MatrixMetalloproteinase Human Fibroblast Collagenase Guanidine Derivatives as Combined Thromboxane A2 Receptor Antagonists andSynthase Inhibitors Synthesis and in Vitro Pharmacology of a Series of New Chiral HistamineH3-Receptor Ligands: 2-(R and S)-Amino-3-(1H-imidazol-4(5)-yl)propyl EtherDerivatives Structure-Based Design, Synthesis, and Biological Evaluation of IrreversibleHuman Rhinovirus 3C Protease Inhibitors. 4. Incorporation of P1 LactamMoieties as l-Glutamine Replacements Docking of Cationic Antibiotics to Negatively Charged Pockets in RNA Folds Enzyme-Assisted Total Synthesis of the Optical Antipodes d-myo-Inositol3,4,5-Trisphosphate and d-myo-Inositol 1,5,6-Trisphosphate: Aspects of TheirStructure−Activity Relationship to Biologically Active Inositol Phosphates Synthesis, Structure−Activity Relationships, and in Vivo Evaluations ofSubstituted Di-tert-butylphenols as a Novel Class of Potent, Selective, andOrally Active Cyclooxygenase-2 Inhibitors. 1. Thiazolone and Oxazolone Series Structure-Based Design, Synthesis, and Biological Evaluation of IrreversibleHuman Rhinovirus 3C Protease Inhibitors. 3. Structure−Activity Studies ofKetomethylene-Containing Peptidomimetics Piperazine Imidazo[1,5-a]quinoxaline Ureas as High-Affinity GABAA Ligands ofDual Functionality 2,3-Diarylcyclopentenones as Orally Active, Highly Selective Cyclooxygenase-2Inhibitors

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