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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_23/m/print http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_23/m/web
Date Copyrighted	2000
Rights	Copyright © 2000 American Chemical Society
issue	23
Rights Holder	American Chemical Society
is Is Part Of of	Design, Synthesis, and Biological Evaluation of Potent and Selective AmidinoBicyclic Factor Xa Inhibitors Chiral Resolution, Pharmacological Characterization, and Receptor Docking ofthe Noncompetitive mGlu1 Receptor Antagonist (±)-2-Hydroxyimino-1a,2-dihydro-1H-7-oxacyclopropa[b]naphthalene-7a-carboxylic Acid Ethyl Ester Reduction-Sensitive Lipopolyamines as a Novel Nonviral Gene Delivery Systemfor Modulated Release of DNA with Improved Transgene Expression Computational Studies on HIV-1 Protease Inhibitors: Influence of CalculatedInhibitor−Enzyme Binding Affinities on the Statistical Quality of 3D-QSARCoMFA Models Therapeutic Opportunities for Muscarinic Receptors in the Central NervousSystem Structure−Function Studies on the New Growth Hormone-Releasing Peptide,Ghrelin: Minimal Sequence of Ghrelin Necessary for Activation of GrowthHormone Secretagogue Receptor 1a S-Acyl-2-thioethyl Aryl Phosphotriester Derivatives as MononucleotideProdrugs Design and Synthesis of Pyrrolidine-5,5-trans-lactams(5-Oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as Novel Mechanism-Based Inhibitorsof Human Cytomegalovirus Protease. 1. The α-Methyl-trans-lactam Template Design, Radiosynthesis, andBiodistribution of a New Potent andSelective Ligand for in Vivo Imaging ofthe Adenosine A2A Receptor SystemUsing Positron Emission Tomography A Selenopyrylium Photosensitizer for Photodynamic Therapy Related inStructure to the Antitumor Agent AA1 with Potent in Vivo Activity and NoLong-Term Skin Photosensitization Syntheses of 4‘-C-Ethynyl-β-d-arabino- and4‘-C-Ethynyl-2‘-deoxy-β-d-ribo-pentofuranosylpyrimidines and -purines andEvaluation of Their Anti-HIV Activity Solid-Phase Synthesis and Biological Evaluation of a Combinatorial Library ofPhilanthotoxin Analogues Biarylpropylsulfonamides as Novel,Potent Potentiators of 2-Amino-3-(5-methyl-3-hydroxyisoxazol-4-yl)-propanoic Acid (AMPA) Receptors Increased DNA Binding Specificity forAntitumor Ecteinascidin 743 throughProtein−DNA Interactions? Molecular Simplification of 1,4-Diazabicyclo[4.3.0]nonan-9-ones GivesPiperazine Derivatives That Maintain High Nootropic Activity Structure−Activity Relationships of 17α-Derivatives of Estradiol as Inhibitorsof Steroid Sulfatase Multiple-Conformation and Protonation-State Representation in 4D-QSAR: The Neurokinin-1 Receptor System Cyanoindole Derivatives as Highly Selective Dopamine D4 Receptor PartialAgonists: Solid-Phase Synthesis, Binding Assays, and Functional Experiments 5-[1‘-(2‘-N-Arylsulfonyl-1‘,2‘,3‘,4‘-tetrahydroisoquinolyl)]-4,5-dihydro-2(3H)-furanones: Positive AllostericModulators of the GABAA Receptor witha New Mode of Action Synthesis, 18F-Labeling, and Biological Evaluation of Piperidyl and PyrrolidylBenzilates as in Vivo Ligands for Muscarinic Acetylcholine Receptors 6-Alkylamino- and 2,3-Dihydro-3‘-methoxy-2-phenyl-4-quinazolinones andRelated Compounds: Their Synthesis, Cytotoxicity, and Inhibition of TubulinPolymerization Novel Design of Nonpeptide AVP V2 Receptor Agonists: StructuralRequirements for an Agonist Having1-(4-Aminobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepine as a Template Synthesis and Evaluation of 17-Aliphatic Heterocycle-Substituted SteroidalInhibitors of 17α-Hydroxylase/C17−20-Lyase (P450 17) Classification of Multidrug-Resistance Reversal Agents Using Structure-BasedDescriptors and Linear Discriminant Analysis Carbonic Anhydrase Inhibitors: Perfluoroalkyl/Aryl-Substituted Derivatives ofAromatic/Heterocyclic Sulfonamides as Topical Intraocular Pressure-LoweringAgents with Prolonged Duration of Action Exploring the Structural Basis of Neurotoxicity in C17-Polyacetylenes Isolatedfrom Water Hemlock

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