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Attributs	Valeurs
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_21/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_21/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	21
Rights Holder	American Chemical Society
is Is Part Of of	Synthesis of Potent C2-Symmetric, Diol-Based HIV-1 Protease Inhibitors.Investigation of Thioalkyl and Thioaryl P1/P1‘ Substituents Potent and Selective ET-A Antagonists. 2. Discovery and Evaluation of Potentand Water Soluble N-(6-(2-(Aryloxy)ethoxy)-4-pyrimidinyl)sulfonamideDerivatives Are Free Energy Calculations Useful in Practice? A Comparison with RapidScoring Functions for the p38 MAP Kinase Protein System Synthesis and Biological Evaluation of s-Triazine Substituted Polyamines asPotential New Anti-Trypanosomal Drugs Hypoxia-Selective Antitumor Agents. 16. Nitroarylmethyl Quaternary Salts asBioreductive Prodrugs of the Alkylating Agent Mechlorethamine Solid-Phase Organic Synthesis. Volume 1 Editedby Anthony W. Czarnik. John Wiley & Sons, New York.2001. viii + 164 pp. 16 × 23.5 cm. ISBN 0-471-31484-6.$69.95. Long Lasting Antinociceptive Properties of Enkephalin Degrading Enzyme(NEP and APN) Inhibitor Prodrugs Discovery of 4-[(Z)-(4-Bromophenyl)-(ethoxyimino)methyl]-1‘-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4‘-methyl-1,4‘-bipiperidine N-Oxide (SCH 351125): AnOrally Bioavailable Human CCR5Antagonist for the Treatment of HIVInfection Synthesis and Antiviral Activity of Novel 5-(1-Cyanamido-2-haloethyl) and5-(1-Hydroxy(or methoxy)-2-azidoethyl) Analogues of Uracil Nucleosides Synthesis of Novel, Potent, Diol-Based HIV-1 Protease Inhibitors viaIntermolecular Pinacol Homocoupling of(2S)-2-Benzyloxymethyl-4-phenylbutanal 1,2-Benzothiazine 1,1-Dioxide P2−P3 Peptide Mimetic Aldehyde Calpain IInhibitors Analytical Chemistry in a GMP Environment: APractical Guide Edited by James M. Miller andJonathan B. Crowther. John Wiley & Sons, Inc., NewYork. 2000. xxiv + 488 pp. 16 × 24 cm. ISBN 0-471-31431-5. $115.00. Synthesis, DNA Cross-Linking Activity, and Cytotoxicity of Dimeric Mitomycins Palmitoyl Derivatives of GpMBP Epitopes: T-Cell Response and PeptidasesSusceptibility Design and Synthesis of a Series of(2R)-N4-Hydroxy-2-(3-hydroxybenzyl)-N-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide Derivatives asPotent, Selective, and Orally BioavailableAggrecanase Inhibitors Statistical Molecular Design, Parallel Synthesis, and Biological Evaluation of aLibrary of Thrombin Inhibitors From Hit to Lead. Analyzing Structure−Profile Relationships Piperazine-Based CCR5 Antagonists asHIV-1 Inhibitors. II. Discovery of1-[(2,4-Dimethyl-3-pyridinyl)carbonyl]-4-methyl-4-[3(S)-methyl-4-[1(S)-[4-(trifluoro-methyl)phenyl]ethyl]-1-piperazinyl]-piperidine N1-Oxide (Sch-350634), anOrally Bioavailable, Potent CCR5Antagonist From Hit to Lead. Combining Two Complementary Methods for FocusedLibrary Design. Application to μ Opiate Ligands Selective Inhibition of ICAM-1 and E-Selectin Expression in Human EndothelialCells. 2. Aryl Modifications of 4-(Aryloxy)thieno[2,3-c]pyridines withFine-Tuning at C-2 Carbamides A New Class of Ibuprofen Derivatives with Reduced Gastrotoxicity Discovery of Macrocyclic HydroxamicAcids Containing BiphenylmethylDerivatives at P1‘, a Series of SelectiveTNF-α Converting Enzyme Inhibitorswith Potent Cellular Activity in theInhibition of TNF-α Release Potent and Selective ET-A Antagonists. 1. Syntheses and Structure−ActivityRelationships of N-(6-(2-(Aryloxy)ethoxy)-4-pyrimidinyl)sulfonamide Derivatives

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