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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_6/m/print http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_6/m/web
Date Copyrighted	1999
Rights	Copyright © 1999 American Chemical Society
issue	6
Rights Holder	American Chemical Society
is Is Part Of of	Novel, Potent, and Selective Phosphodiesterase-4 Inhibitors as AntiasthmaticAgents: Synthesis and Biological Activities of a Series of 1-PyridylnaphthaleneDerivatives Thieno[3,2-b]- and Thieno[2,3-b]pyrrole Bioisosteric Analogues of theHallucinogen and Serotonin Agonist N,N-Dimethyltryptamine Melatonergic Properties of the (+)- and (−)-Enantiomers ofN-(4-Methoxy-2,3-dihydro-1H-phenalen-2-yl)amide Derivatives Strategies for Organic Drug Synthesis andDesign By Daniel Lednicer. John Wiley & Sons, Inc.,New York. 1998. xv + 502 pp. 16.5 × 24 cm. ISBN0-471-19657-6. $79.95. Design, Synthesis, and Evaluation of Conformationally Constrained Tongs, NewInhibitors of HIV-1 Protease Dimerization Structure−Activity Relationships of Lysophosphatidic Acid: ConformationallyRestricted Backbone Mimetics Design, Synthesis, Structure−Activity Relationships, and BiologicalCharacterization of Novel Arylalkoxyphenylalkylamine σ Ligands as PotentialAntipsychotic Drugs Postsynthetic Generation of a MajorAcrolein Adduct of 2‘-Deoxyguanosine inOligomeric DNA† Diversity Analysis of 14 156 Molecules Tested by the National Cancer Institutefor Anti-HIV Activity Using the Quantitative Structure−Activity RelationalExpert System MCASE Synthesis and Antiparasitic and Antitumor Activity of 2,4-Diamino-6-(arylmethyl)-5,6,7,8-tetrahydroquinazoline Analogues of Piritrexim Glutathione-Mediated Metabolism of Technetium-99m SNS/S Mixed LigandComplexes: A Proposed Mechanism of Brain Retention Metal-catalyzed Cross-coupling Reactions Editedby François Diederich and Peter J. Stang. Wiley−VCH,Weinheim. 1998. xxi + 517 pp. 17 × 25 cm. ISBN 3-527-29421-X. $140.00. 6-Substituted Benzopyrans as Potassium Channel Activators: Synthesis,Vasodilator Properties, and Multivariate Analysis Cytotoxicity of (2,2‘:6‘,2‘ ‘-Terpyridine)platinum(II) Complexes to Leishmaniadonovani, Trypanosoma cruzi, and Trypanosoma brucei Discovery of a Novel Class of Selective Non-Peptide Antagonists for the HumanNeurokinin-3 Receptor. 2. Identification of (S)-N-(1-Phenylpropyl)-3-hydroxy-2-phenylquinoline-4-carboxamide (SB 223412) Bis- and Mixed-Tetrahydroisoquinolinium Chlorofumarates: NewUltra-Short-Acting Nondepolarizing NeuromuscularBlockers Use of a Pharmacophore Model for the Design of EGFR Tyrosine KinaseInhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones Structure-based Ligand Design Edited by K. Gubernator and H.-J. Bohm. Wiley-VCH, Weinheim. 1998.xiv + 153 pp. 17.5 × 24.5 cm. ISBN 3-527-29343-4.$135.00. Synthesis, Pharmacological Characterization, and Molecular Modeling ofHeterobicyclic Amino Acids Related to (+)-2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic Acid (LY354740): Identification of Two New Potent, Selective,and Systemically Active Agonists for Group II Metabotropic GlutamateReceptors Structure−Activity Relationship of Diaryl Phosphonate Esters as PotentIrreversible Dipeptidyl Peptidase IV Inhibitors Structural and Conformational Requirements for High-Affinity Binding to theSH2 Domain of Grb2 Novel Inhibitors of Carboxypeptidase G2 (CPG2): Potential Use inAntibody-Directed Enzyme Prodrug Therapy

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