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type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_24/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_24/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	24
Rights Holder	American Chemical Society
is Is Part Of of	Methyl Analogues of the Experimental Alzheimer Drug Phenserine: Synthesisand Structure/Activity Relationships for Acetyl- and ButyrylcholinesteraseInhibitory Action Novel Agouti-Related-Protein-Based Melanocortin-1 Receptor Antagonist 5,6-Diphenylpyridazine Derivatives as Acyl-CoA:Cholesterol AcyltransferaseInhibitors Synthesis and Antibacterial Activity ofAcylides (3-O-Acyl-erythromycinDerivatives): A Novel Class of MacrolideAntibiotics The Biological Effects of Structural Variation at the Meta Position of theAromatic Rings and at the End of the Alkenyl Chain in theAlkenyldiarylmethane Series of Non-Nucleoside Reverse TranscriptaseInhibitors 5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-Based Potentand Selective CCK1 Receptor Antagonists: Structure−Activity RelationshipStudies on the Central 1,3-Dioxoperhydropyrido[1,2-c]pyrimidine Scaffold Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic AcidDerivatives as Bone Anabolic Agents for the Treatment of Osteoporosis Cytokine Inhibitors Edited by Gennaro Cilibertoand Rocco Savino. Marcel Dekker, New York. 2001. xiv+ 372 pp. 15.5 × 23.5 cm. ISBN 0-0434-7. $165.00. Role of Hydrophilic Interaction in Binding of Hydroxylated 3-Deoxy C19Steroids to the Active Site of Aromatase Synthesis and Biological Evaluation of Prostaglandin-F Alkylphosphinic Acid Derivatives as BoneAnabolic Agents for the Treatment of Osteoporosis. Synthesis and Antiviral Activity of Novel Acyclic Nucleoside Analogues of5-(1-Azido-2-haloethyl)uracils Salicylaldoxime Moiety as a Phenolic “A-Ring” Substitute in Estrogen ReceptorLigands Advances in Protein Chemistry. Volume 56. DrugDiscovery and Design Edited by Edward M. Scolnick.Academic Press, San Diego, CA. 2000. xi + 567 pp. 16× 23.5 cm. ISBN 0-12-034256-1. $119.95. Design, Synthesis, and Biological Activityof Methoctramine-Related Polyamines asPutative Gi Protein Activators Metal Ions in Biological Systems. Volume 38.Probing of Proteins by Metal Ions and TheirLow Molecular Weight Complexes Edited byAstrid Sigel and Helmut Sigel. Marcel Dekker, NewYork. 2001. xlvii + 690 pp. 16 × 23.5 cm. ISBN 0-8247-0289-1. $250.00. The Synthesis of a Prodrug of Doxorubicin Designed to Provide ReducedSystemic Toxicity and Greater Target Efficacy Neoceptor Concept Based on Molecular Complementarity in GPCRs: A MutantAdenosine A3 Receptor with Selectively Enhanced Affinity for Amine-ModifiedNucleosides An Orally Active, Water-Soluble Neurokinin-1 Receptor Antagonist Suitable forBoth Intravenous and Oral Clinical Administration Design and Pharmacological Activity of Phosphinic Acid Based NAALADaseInhibitors Discovery and Biological Evaluation of a New Family of Potent Inhibitors ofthe Dual Specificity Protein Phosphatase Cdc25 Rational Design, Discovery, and Synthesis of a Novel Series of Potent GrowthHormone Secretagogues Estrogen Receptor-β Potency-Selective Ligands: Structure−ActivityRelationship Studies of Diarylpropionitriles and Their Acetylene and PolarAnalogues Design of Selective and Soluble Inhibitors of Tumor Necrosis Factor-αConverting Enzyme (TACE) Design and Optimization of 20-O-Linked Camptothecin Glycoconjugates asAnticancer Agents Combinatorial Chemistry Edited by Hicham Fenniri. 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Novel Nicotinic Antagonist Design, Synthesis, and Transfection Biology of Novel Cationic Glycolipids forUse in Liposomal Gene Delivery N-[3-(2-Dimethylaminoethyl)-2-methyl-1H-indol-5-yl]-4-fluorobenzamide: A Potent,Selective, and Orally Active 5-HT1FReceptor Agonist Potentially Useful forMigraine Therapy Solid Phase Synthesis. Edited by Kevin Burgess.Wiley Interscience, New York. 2000. xiv + 277 pp. 15.5× 23.5 cm. ISBN 0471318256. $69.95. Novel Erythromycin Derivatives with Aryl Groups Tethered to the C-6 PositionAre Potent Protein Synthesis Inhibitors and Active against Multidrug-ResistantRespiratory Pathogens Solid PhaseSynthesis: A Practical Guide Editedby Steven A. Kates and Fernando Albericio. MarcelDekker, Inc., New York. 2000. xx + 826 pp. 15.5 × 24cm. ISBN 0-8247-0359-6. $250.00. Fluorescent Tricyclic Analogues of Acyclovir and Ganciclovir.A Structure−Antiviral Activity Study

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