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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_23/m/print http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_23/m/web
Date Copyrighted	1997
Rights	Copyright © 1997 American Chemical Society
issue	23
Rights Holder	American Chemical Society
is Is Part Of of	Antimuscarinic 3-(2-Furanyl)quinuclidin-2-ene Derivatives: Synthesis andStructure−Activity Relationships Combinatorial Chemistry. Synthesis and Application Edited by Stephen R. Wilson and Anthony W.Czarnik. John Wiley & Sons. 1997. ix + 269 pp. 16× 24 cm. ISBN 0-471-12687-X. $69.95. Burgers' Medicinal Chemistry and Drug Discovery. Volume 4 Edited by M. E. Wolff. John Wiley &Sons, New York. 1997. viii + 656 pp. 18.5 × 26 cm.ISBN 0-471-57559-3. $225.00. Design, Synthesis, and Cocrystal Structure of a Nonpeptide Src SH2 DomainLigand Studies in Medicinal Chemistry. Volume 2. Biological Inhibitors Edited by M. Iqbal Choudhary.Harwood Academic Publishers GmbH, Amsterdam.1996. xiv + 378 pp. 17.5 × 25.3 cm. ISBN 3-7186-5879-8. $150.00. Retinoic Acid Conjugates as Potential Antitumor Agents: Synthesis andBiological Activity of Conjugates with Ara-A, Ara-C, 3(2H)-Furanone, andAniline Mustard Moieties Synthesis and Evaluation of (S)-4-(3-(2‘-[11C]Isopropylamino)-2-hydroxypropoxy)-2H-benzimidazol-2-one ((S)-[11C]CGP 12388) and (S)-4-(3-((1‘-[18F]Fluoroisopropyl)amino)-2-hydroxypropoxy)-2H-benzimidazol-2-one((S)-[18F]Fluoro-CGP 12388) for Visualization of β-Adrenoceptors with PositronEmission Tomography Synthesis and Structure−Activity Profiles of A-Homoestranes, theEstratropones Design, Synthesis, and Biochemical Evaluation of Phosphonate andPhosphonamidate Analogs of Glutathionylspermidine as Inhibitors ofGlutathionylspermidine Synthetase/Amidase from Escherichia coli Betidamino Acid Scan of the GnRH Antagonist Acyline 1-[(ω-Aminoalkyl)amino]-4-[N-(ω-aminoalkyl)carbamoyl]-9-oxo-9,10-dihydro-acridines as Intercalating Cytotoxic Agents: Synthesis, DNA Binding, andBiological Evaluation 1,4-Disubstituted Anthracene Antitumor Agents The Chemistry of Mind-Altering Drugs. History,Pharmacology, and Cultural Context By DanielM. Perrine. American Chemical Society, Washington,D.C. 1996. x + 480 pp. 17.5 × 25 cm. ISBN 0-8412-3253-9. $39.95. 4-Hydroxy-5,6-dihydropyrones. 2. Potent Non-Peptide Inhibitors of HIVProtease Discovery of a Novel, Selective, and Orally Bioavailable Class of ThrombinInhibitors Incorporating Aminopyridyl Moieties at the P1 Position Design and Synthesis of Imidazoline Derivatives Active on Glucose Homeostasisin a Rat Model of Type II Diabetes. 1. Synthesis and Biological Activities ofN-Benzyl-N ‘-(arylalkyl)-2-(4‘,5‘-dihydro-1‘H-imidazol-2‘-yl)piperazines Synthesis and Biological Activity of a Series of Potent Fluoromethyl KetoneInhibitors of Recombinant Human Calpain I Potent and Selective 1,2,3-TrisubstitutedIndole NPY Y-1 Antagonists Synthesis and Biological Evaluation of 4-(Hydroxyalkyl)estradiols and RelatedCompounds Simple Analogues of Anthralin: Unusual Specificity of Structure andAntiproliferative Activity N6-Cyclopentyl-3‘-substituted-xylofuranosyladenosines: A New Class ofNon-Xanthine Adenosine A1 Receptor Antagonists Synthesis and Antimalarial Activity in Vitro and in Vivo of a NewFerrocene−Chloroquine Analogue Synthesis of 5,6-Dihydro-4-hydroxy-2-pyrones as HIV-1 Protease Inhibitors: The Profound Effect of Polarity onAntiviral Activity

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