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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_26/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_26/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	26
Rights Holder	American Chemical Society
is Is Part Of of	Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−ActivityRelationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted2-Aminoindans Design and Synthesis of Non-peptidic Inhibitors for the Syk C-Terminal SH2Domain Based on Structure-Based In-Silico Screening Principles and Applications of Asymmetric Synthesis By Guo-Qiang Lin, Yue-Ming Li, and Albert S.C. Chan. Wiley Interscience, New York. 2001. xvii + 515pp. 16 × 24 cm. ISBN 0-471-40027-0. $89.95. Chemosensitization of a Multidrug-Resistant Leishmania tropica Line by NewSesquiterpenes from Maytenus magellanica and Maytenus chubutensis Identification of Dipeptidyl Nitriles as Potent and Selective Inhibitors ofCathepsin B through Structure-Based Drug Design A Novel Approach for the Development of Selective Cdk4 Inhibitors: LibraryDesign Based on Locations of Cdk4 Specific Amino Acid Residues Quadruplex-Interactive Agents as Telomerase Inhibitors: Synthesis ofPorphyrins and Structure−Activity Relationship for the Inhibition ofTelomerase Synthesis, Biological Evaluation, and Pharmacophore Generation of Uracil,4(3H)-Pyrimidinone, and Uridine Derivatives as Potent and Selective Inhibitorsof Parainfluenza 1 (Sendai) Virus Mononuclear Platinum(II) Complex with 2-Phenylpyridine Ligands ShowingHigh Cytotoxicity against Mouse Sarcoma 180 Cells Acquiring High CisplatinResistance Structure of Protein Tyrosine Phosphatase 1B in Complex with InhibitorsBearing Two Phosphotyrosine Mimetics Characterization of the1H-Cyclopentapyrimidine-2,4(1H,3H)-dioneDerivative (S)-CPW399 as a Novel,Potent, and Subtype-Selective AMPAReceptor Full Agonist with PartialDesensitization Properties Synthesis and Biological Evaluation ofMyoseverin Derivatives: MicrotubuleAssembly Inhibitors Design, Synthesis and BiologicalEvaluation of Novel Arachidonic AcidDerivatives as Highly Potent andSelective Endocannabinoid TransporterInhibitors Dimerization of G-Protein-Coupled Receptors Diaminoindanes as Microsomal Triglyceride Transfer Protein Inhibitors Oxindole Derivatives as Orally Active Potent Growth Hormone Secretagogues 2-(2-Piperidyl)- and 2-(2-Pyrrolidyl)chromans as Nicotine Agonists: Synthesisand Preliminary Pharmacological Characterization Synthesis and Antitumor Activity of Novel C-7 Paclitaxel Ethers: Discovery ofBMS-184476 Synthesis and Applications of IsotopicallyLabelled Compounds. Volume 7. Proceedings ofthe Seventh International Symposium, Dresden,Germany, June 18−22, 2000 Edited by U. Pleissand R. Voges. Wiley, New York. 2001. xxv + 702 pp.17 × 25 cm. ISBN 0-471-49501-8. $220.00. Synthetic 2-Aroylindole Derivatives as a New Class of PotentTubulin-Inhibitory, Antimitotic Agents Structural Basis for the Binding Affinity of Xanthines with the DNAIntercalator Acridine Orange Design, Synthesis, and Pharmacological Evaluation of Thapsigargin Analoguesfor Targeting Apoptosis to Prostatic Cancer Cells C-16 Artemisinin Derivatives and Their Antimalarial and Cytotoxic Activities: Syntheses of Artemisinin Monomers, Dimers, Trimers, and Tetramers byNucleophilic Additions to Artemisitene Synthesis, in Vitro Pharmacology, and Molecular Modeling of syn-Huprines asAcetylcholinesterase Inhibitors Design, Synthesis, and Biological Characterization of Bivalent1-Methyl-1,2,5,6-tetrahydropyridyl-1,2,5-thiadiazole Derivatives as SelectiveMuscarinic Agonists Structure-Based Generation of a New Class of Potent Cdk4 Inhibitors: New deNovo Design Strategy and Library Design

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