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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_14/m/print http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_14/m/web
Date Copyrighted	2004
Rights	Copyright © 2004 American Chemical Society
issue	14
Rights Holder	American Chemical Society
is Is Part Of of	Identification of Non-Phosphate-Containing Small Molecular Weight Inhibitorsof the Tyrosine Kinase p56 Lck SH2 Domain via in Silico Screening against thepY + 3 Binding Site Total Synthesis and Anti-Tubulin Activity of Epi-C3 Analogues ofCryptophycin-24 Design, Synthesis, and Biological Evaluation of2,4-Diamino-5-methyl-6-substituted-pyrrolo[2,3-d]pyrimidines as DihydrofolateReductase Inhibitors Conjugates of Gadolinium Complexes to Bile Acids as Hepatocyte-DirectedContrast Agents for Magnetic Resonance Imaging Novel Dicationic Imidazo[1,2-a]pyridines and5,6,7,8-Tetrahydro-imidazo[1,2-a]pyridines as Antiprotozoal Agents New 2,4-Diamino-5-(2‘,5‘-substituted benzyl)pyrimidines as Potential Drugs against Opportunistic Infections of AIDS and Other Immune Disorders.Synthesis and Species-Dependent Antifolate Activity Synthesis, Characterization, and Preliminary in Vivo Tests of New Poly(ethylene glycol) Conjugates of the Antitumor Agent 10-Amino-7-ethylcamptothecin 3-(2-Aminoalkyl)-1-(2,6-difluorobenzyl)-5-(2-fluoro-3-methoxyphenyl)-6-methyl-uracils as Orally BioavailableAntagonists of the Human GonadotropinReleasing Hormone Receptor Development of Potent Bifunctional Endomorphin-2 Analogues with Mixedμ-/δ-Opioid Agonist and δ-Opioid Antagonist Properties Inhibition of Group IVA Cytosolic Phospholipase A2 by Novel 2-Oxoamides inVitro, in Cells, and in Vivo Frontiers in Medicinal ChemistryOnline. Volume 1 (online book series) Edited by Atta-ur-Rahman and A. B. Reitz. Bentham Science Publishers,Ltd. (http://www.bentham.org/). 2004. vi + 688 pp. CDROM $245.00 or $45.00 per Chapter Online. Hydrophobic Acetal and KetalDerivatives of Mannopeptimycin-α andDesmethylhexahydromannopeptimycin-α: Semisynthetic Glycopeptides with PotentActivity Against Gram-Positive Bacteria Antagonist Analogue of6-[3‘-(1-Adamantyl)-4‘-hydroxyphenyl]-2-naphthalenecarboxylic Acid (AHPN)Family of Apoptosis Inducers That Effectively Blocks AHPN-Induced Apoptosisbut Not Cell-Cycle Arrest Uncharged AZT and D4T Derivatives of Phosphonoformic and PhosphonoaceticAcids as Anti-HIV Pronucleosides Synthesis, Biological Activity, and Three-Dimensional QuantitativeStructure−Activity Relationship Model for a Series ofBenzo[c]quinolizin-3-ones, Nonsteroidal Inhibitors of Human Steroid5α-Reductase 1 Tiplaxtinin, a Novel, Orally EfficaciousInhibitor of Plasminogen ActivatorInhibitor-1: Design, Synthesis, andPreclinical Characterization Dye-Labeled Benzodiazepines: Development of Small Ligands for ReceptorBinding Studies Using Fluorescence Correlation Spectroscopy Probing the Pharmacophore for Allosteric Ligands of Muscarinic M2 Receptors: SAR and QSAR Studies in a Series of Bisquaternary Salts of Caracurine V andRelated Ring Systems Computer-Assisted Design of Selective Imidazole Inhibitors for CytochromeP450 Enzymes Synthesis and Biological Evaluation of3-Heterocyclyl-7,8,9,10-tetrahydro-(7,10-ethano)-1,2,4-triazolo[3,4-a]phthalazinesand Analogues as Subtype-Selective Inverse Agonists for the GABAAα5Benzodiazepine Binding Site Synthesis and Antibacterial Activity of a Novel Series of Potent DNA GyraseInhibitors. Pyrazole Derivatives Identification, Synthesis, and Characterization of New Glycogen PhosphorylaseInhibitors Binding to the Allosteric AMP Site Mechanism of Inactivation of β-Lactamases by Novel 6-Methylidene PenemsElucidated Using Electrospray Ionization Mass Spectrometry New Manzamine Alkaloids from an Indo-Pacific Sponge. Pharmacokinetics,Oral Availability, and the Significant Activity of Several Manzamines againstHIV-I, AIDS Opportunistic Infections, and Inflammatory Diseases Inhibition of Cytokine Production by Hymenialdisine Derivatives 1,2,4-Triazolo[4,3-a]quinoxalin-1-one Moiety as an Attractive Scaffold ToDevelop New Potent and Selective Human A3 Adenosine Receptor Antagonists: Synthesis, Pharmacological, and Ligand−Receptor Modeling Studies DNA Binding To Guide the Development ofTetrahydroindeno[1,2-b]pyrido[4,3,2-de]quinoline Derivatives as CytotoxicAgents Fragment-Based Drug Discovery Catalase-Mediated Nitric Oxide Formation from Hydroxyurea Studies in Natural Products Chemistry. Volume29. Bioactive Natural Products (Part J) Edited byAtta-ur-Rahman. Elsevier, New York. 2003. x + 902 pp.16.5 × 24.5 cm. ISBN 0-444-51510-0. $410.00.

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