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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_11/m/print http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_11/m/web
Date Copyrighted	1997
Rights	Copyright © 1997 American Chemical Society
issue	11
Rights Holder	American Chemical Society
is Is Part Of of	Structure−Activity Relationships ofN2-Aryl-3-(isoxazolylsulfamoyl)-2-thiophenecarboxamides as SelectiveEndothelin Receptor-A Antagonists 1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2 Substituted Hexahydrobenzo[f]thieno[c]quinolines as Dopamine D1-SelectiveAgonists: Synthesis and Biological Evaluation in Vitro and in Vivo The Dopamine Receptors Edited by K. A. Neve andR. L. Neve. Humana Press, Totowa, NJ. 1997. xi +533 pp. 16 × 23 cm. ISBN-0-89603. $119.50. Synthesis, Structure, and Antiproliferative Activity of Selenophenfurin, anInosine 5‘-Monophosphate Dehydrogenase Inhibitor Analogue of Selenazofurin 1,2-Diarylimidazoles as Potent, Cyclooxygenase-2 Selective, and Orally ActiveAntiinflammatory Agents Aroyl(aminoacyl)pyrroles, a New Class of Anticonvulsant Agents Design, Synthesis, and Evaluation of Tetrahydropyrimidinones as an Exampleof a General Approach to Nonpeptide HIV Protease Inhibitors Biological and Conformational Examination of Stereochemical ModificationsUsing the Template Melanotropin Peptide, Ac-Nle-c[Asp-His-Phe-Arg-Trp-Ala-Lys]-NH2, on Human Melanocortin Receptors Modulation of Melphalan Resistance in Glioma Cells with a PeripheralBenzodiazepine Receptor Ligand−Melphalan Conjugate Halogenated 4-(Phenoxymethyl)piperidines as Potential Radiolabeled Probesfor σ-1 Receptors: In Vivo Evaluation of[123I]-1-(Iodopropen-2-yl)-4-[(4-cyanophenoxy)methyl]piperidine Synthesis and Structure−Activity Relationships of a New Model ofArylpiperazines. 2. Three-Dimensional Quantitative Structure−ActivityRelationships of Hydantoin−Phenylpiperazine Derivatives with Affinity for5-HT1A and α1 Receptors. A Comparison of CoMFA Models Synthesis and Oral Efficacy of a 4-(Butylethylamino)pyrrolo[2,3-d]pyrimidine: A Centrally Active Corticotropin-Releasing Factor1 Receptor Antagonist Discovery of TBC11251, a Potent, Long Acting, Orally Active EndothelinReceptor-A Selective Antagonist Dual Metalloprotease Inhibitors: Mercaptoacetyl-Based Fused HeterocyclicDipeptide Mimetics as Inhibitors of Angiotensin-Converting Enzyme andNeutral Endopeptidase 7-Spiroindanyl Derivatives of Naltrexone and Oxymorphone as SelectiveLigands for δ Opioid Receptors Potent Noncovalent Thrombin Inhibitors That Utilize the Unique Amino Acidd-Dicyclohexylalanine in the P3 Position. Implications on Oral Bioavailabilityand Antithrombotic Efficacy Books of Interest Chemometric Methodologies in a Quantitative Structure−Activity RelationshipStudy: The Antibacterial Activity of 6-Aminoquinolones 17β-(3-Furyl)-5β-androstane-3β,14β,17α-triol(PST 2238). A Very PotentAntihypertensive Agent with a NovelMechanism of Action Arylcarbamate Derivatives of 1-Piperidineethanol as Potent Ligands for 5-HT4Receptors Synthesis and Pharmacological Properties of a Close Analogue of anAntithrombotic Pentasaccharide (SR 90107A/ORG 31540) Anesthetic Activity of Novel Water-Soluble 2β-Morpholinyl Steroids and TheirModulatory Effects at GABAA Receptors Anticancer and Antiviral Effects and Inactivation of S-Adenosyl-l-homocysteineHydrolase with 5‘-Carboxaldehydes and Oximes Synthesized from Adenosineand Sugar-Modified Analogues

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