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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_8/m/print http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_8/m/web
Date Copyrighted	1997
Rights	Copyright © 1997 American Chemical Society
issue	8
Rights Holder	American Chemical Society
is Is Part Of of	Synthesis and Transporter Binding Properties of 2,3-DiphenyltropaneStereoisomers. Comparison to 3β-Phenyltropane-2β-carboxylic Acid Esters N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines: Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor Mustard Prodrugs for Activation by Escherichia coli Nitroreductase inGene-Directed Enzyme Prodrug Therapy Arylamide Inhibitors of HIV-1 Integrase The Practical Synthesis of a Methylenebisphosphonate Analogue of BenzamideAdenine Dinucleotide: Inhibition of Human Inosine MonophosphateDehydrogenase (Type I and II) Redox Pathway Leading to the Alkylation of DNA by the Anthracycline,Antitumor Drugs Adriamycin and Daunomycin Inhibition of Uridine Phosphorylase. Synthesis and Structure−ActivityRelationships of Aryl-Substituted1-((2-Hydroxyethoxy)methyl)-5-(3-phenoxybenzyl)uracil Correlation of Selective Modifications to a2‘,5‘-Oligoadenylate−3‘,5‘-Deoxyribonucleotide Antisense Chimera with Affinityfor the Target Nucleic Acid and with Ability To Activate RNase L 1-Aryl-3,5-dihydro-4H-2,3-benzodiazepin-4-ones: Novel AMPA ReceptorAntagonists Selecting Optimally Diverse Compounds from Structure Databases: AValidation Study of Two-Dimensional and Three-Dimensional MolecularDescriptors The Discovery of Potent IsoxazolineGlycoprotein IIb/IIIa Receptor Antagonists Synthesis and Biological Characterization of 1,4,5,6-Tetrahydropyrimidine and2-Amino-3,4,5,6-tetrahydropyridine Derivatives as Selective m1 Agonists Novel Indole-2-carboxamide and Cycloalkeno[1,2-b]indole Derivatives.Structure−Activity Relationships for High Inhibition of Human LDLPeroxidation Synthesis and Opioid Activity of Conformationally Constrained Dynorphin AAnalogues. 2. Conformational Constraint in the “Address” Sequence,

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