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type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_18/m/print http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_18/m/web
Date Copyrighted	1998
Rights	Copyright © 1998 American Chemical Society
issue	18
Rights Holder	American Chemical Society
is Is Part Of of	A Scoring Scheme for Discriminating between Drugs and Nondrugs Synthesis of 9-Deoxo-4‘‘-deoxy-6,9-epoxyerythromycin Derivatives: Novel andAcid-Stable Motilides Pyrazole Bioisosteres of Leflunomide as B-Cell Immunosuppressants forXenotransplantation and Chronic Rejection: Scope and Limitations 3-Deoxy-d-myo-inositol 1-Phosphate,1-Phosphonate, and Ether LipidAnalogues as Inhibitors ofPhosphatidylinositol-3-kinase Signalingand Cancer Cell Growth Synthesis and Biological Activity of 4-Amino-7-oxo-Substituted Analogues of5-Deaza-5,6,7,8-tetrahydrofolic Acid and 5,10-Dideaza-5,6,7,8-tetrahydrofolicAcid Anticonvulsant Activity and Interactions with Neuronal Voltage-DependentSodium Channel of Analogues of Ameltolide 4-Benzylamino-1-chloro-6-substituted Phthalazines: Synthesis and InhibitoryActivity toward Phosphodiesterase 5 Physical Parameters and Biological Stability of Yttrium(III)Diethylenetriaminepentaacetic Acid Derivative Conjugates Small Molecular Probes for G-Protein-Coupled C5a Receptors: Conformationally Constrained Antagonists Derived from the C Terminus of theHuman Plasma Protein C5a Methods in Molecular Biology, Volume 87. Combinatorial Peptide Library Protocols Edited byShmuel Cabilly. Humana Press, Totowa, NJ. 1998. xiii+ 313 pp. 15.5 × 23.5 cm. ISBN 0-89603-392-9.$74.50. Synthesis and Antiallergic Activity ofDimethyl-2-(phenylcarbamoyl)ethylsulfonium p-Toluenesulfonate Derivatives New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 ProteaseInhibitors: Candidates for Clinical Development Discovery and Preliminary SAR Studies of a Novel, Nonsteroidal ProgesteroneReceptor Antagonist Pharmacophore Synthesis, Physicochemical Properties, and Evaluation ofN-Substituted-2-alkyl-3-hydroxy-4(1H)-pyridinones Design and Synthesis of Brefeldin A Sulfide Derivatives as Prodrug Candidateswith Enhanced Aqueous Solubilities Structure−Activity Study of the Nociceptin(1−13)-NH2 N-Terminal Tetrapeptideand Discovery of a Nociceptin Receptor Antagonist Studies of Structure−Activity Relationship of Nitroxide Free Radicals andTheir Precursors as Modifiers Against Oxidative Damage Structure−Activity Relationships for a Series of Bis(phenylalkyl)amines: Potent Subtype-Selective Inhibitors of N-Methyl-d-aspartate Receptors New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 3.7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as GastrointestinalSafe Antiinflammatory and Analgesic Agents: Variations at the 5 Position β-Amino-thiols Inhibit the Zinc Metallopeptidase Activity of Tetanus ToxinLight Chain Tipranavir (PNU-140690): A Potent, Orally Bioavailable Nonpeptidic HIVProtease Inhibitor of the 5,6-Dihydro-4-hydroxy-2-pyrone Sulfonamide Class Can We Learn To Distinguish between “Drug-like” and “Nondrug-like”Molecules? Synthesis and Biological Activity of Conformationally Restricted Analogues ofMilnacipran: (1S,2R)-1-Phenyl-2-[(R)-1-amino-2-propynyl]-N,N-diethylcyclopropanecarboxamide Is a Novel Class of NMDA Receptor ChannelBlocker 3,5-Dihydro-4H-2,3-benzodiazepine-4-thiones: A New Class of AMPA ReceptorAntagonists Structure-Based Design and Synthesis of Lipophilic 2,4-Diamino-6-SubstitutedQuinazolines and Their Evaluation as Inhibitors of Dihydrofolate Reductasesand Potential Antitumor Agents Synthesis and Evaluation of2-Amino-9-(3-hydroxymethyl-4-alkoxycarbonyloxybut-1-yl)purines as PotentialProdrugs of Penciclovir The P2 Nucleotide Receptors Edited by John T.Turner, Gary A. Weisman, and Jeffrey S. Fedan. Humana Press, Totowa, NJ. 1997. xi + 440 pp. 16 × 23.5cm. ISBN 0-89603-425-9. $139.00. Conformational Analysis of Ketolide, Conformations of RU 004 in Solution andBound to Bacterial Ribosomes Structure-Based Design and Synthesis of High Affinity Tripeptide Ligands ofthe Grb2-SH2 Domain 3-Alkyl Ethers of Clocinnamox: Delayed Long-Term μ-Antagonists withVariable μ Efficacy

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