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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/m/print http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/m/web
Date Copyrighted	2005
Rights	Copyright © 2005 American Chemical Society
issue	20
Rights Holder	American Chemical Society
is Is Part Of of	Inhibitors of Apoptosis in Lymphocytes: Synthesis and Biological Evaluation ofCompounds Related to Pifithrin-α Synthesis and Structure−Activity Relationship of the First NonpeptidergicInverse Agonists for the Human Cytomegalovirus Encoded ChemokineReceptor US28 Synthesis and SAR of 5-Amino- and 5-(Aminomethyl)benzofuran Histamine H3Receptor Antagonists with Improved Potency A Novel Series of Non-Carboxylic Acid, Non-Hydantoin Inhibitors of AldoseReductase with Potent Oral Activity in Diabetic Rat Models: 6-(5-Chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and Congeners 5-Cyanopyrimidine Derivatives as a Novel Class of Potent, Selective, and OrallyActive Inhibitors of p38α MAP Kinase Design, Synthesis, and Preliminary Pharmacological Evaluation of a Set ofSmall Molecules That Directly Activate Gi Proteins Indole-3-acetic Acid Antagonists of theProstaglandin D2 Receptor CRTH2 Modeling Water Molecules in Protein−Ligand Docking Using GOLD Synthesis and Antiinflammatory Activity of Coumarin Derivatives, High Affinity Electrophilic and Photoactivatable Covalent EndocannabinoidProbes for the CB1 Receptor Synthesis, Binding Affinity at Glutamic Acid Receptors, NeuroprotectiveEffects, and Molecular Modeling Investigation of Novel Dihydroisoxazole AminoAcids Adenosine Kinase Inhibitors. 5. Synthesis, Enzyme Inhibition, and AnalgesicActivity of Diaryl-erythro-furanosyltubercidin Analogues Synthesis and Pharmacological Evaluation of 1H-Imidazoles as Ligands for theEstrogen Receptor and Cytotoxic Inhibitors of the Cyclooxygenase Pharmacophore Modeling, Docking, and Principal Component Analysis BasedClustering: Combined Computer-Assisted Approaches To Identify NewInhibitors of the Human Rhinovirus Coat Protein Design, Synthesis, and Activity of Analogues of Phosphinothricin as Inhibitorsof Glutamine Synthetase Synthesis of an Estrogen Receptor β-Selective Radioligand: 5-[18F]Fluoro-(2R,3S)-2,3-bis(4-hydroxyphenyl)pentanenitrile and Comparisonof in Vivo Distribution with 16α-[18F]Fluoro-17β-estradiol Unambiguous Synthesis and Prophylactic Antimalarial Activities ofImidazolidinedione Derivatives Design, Synthesis, and Biological Activity of m-Tyrosine-Based 16- and17-Membered Macrocyclic Inhibitors of Hepatitis C Virus NS3 Serine Protease Glycodiversification for the Optimization of the Kanamycin ClassAminoglycosides Synthesis of Leukotriene B4 Antagonists Labeled with In-111 or Tc-99m toImage Infectious and Inflammatory Foci Acyl Ureas as Human Liver Glycogen Phosphorylase Inhibitors for theTreatment of Type 2 Diabetes Ligand Recognition by RAR and RXR Receptors: Binding and Selectivity Alkyl-Substituted Polyaminohydroxamic Acids: A Novel Class of TargetedHistone Deacetylase Inhibitors Reagents for High-Throughput Solid-Phase andSolution-Phase Organic Synthesis Edited by PeterWipf. John Wiley & Sons, Chichester, West Sussex,England. 2005. xi + 380 pp. 22 × 29 cm. ISBN 0-470-86298-X. $140.00. Potent Cannabinergic Indole Analogues as Radioiodinatable Brain ImagingAgents for the CB1 Cannabinoid Receptor Synthesis and Biological Evaluation of Spin-Labeled Alkylphospholipid Analogs Molecular Modeling of Wild-Type and D816V c-Kit Inhibition Based onATP-Competitive Binding of Ellipticine Derivatives to Tyrosine Kinases Design and Synthesis of Specific Probes for Human 5-HT4 ReceptorDimerization Studies Discovery of N-(2,6-Dimethylphenyl)-Substituted Semicarbazones asAnticonvulsants: Hybrid Pharmacophore-Based Design Simple but Highly Effective Three-Dimensional Chemical-Feature-BasedPharmacophore Model for Diketo Acid Derivatives as Hepatitis C VirusRNA-Dependent RNA Polymerase Inhibitors Synthesis and Structure−Activity Relationships of Novel Anti-hepatitis CAgents: N3,5‘-Cyclo-4-(β-d-ribofuranosyl)-vic-triazolo[4,5-b]pyridin-5-oneDerivatives Multimodality Agents for Tumor Imaging (PET, Fluorescence) andPhotodynamic Therapy. A Possible “See and Treat” Approach Discovery of Potent3,5-Diphenyl-1,2,4-oxadiazoleSphingosine-1-phosphate-1 (S1P1)Receptor Agonists with ExceptionalSelectivity against S1P2 and S1P3 Structure−Activity Relationships of New A,D-Ring Modified Steroids asAromatase Inhibitors: Design, Synthesis, and Biological Activity Evaluation Structure−Activity Studies of Peptides from the “Hot-Spot” Region of HumanCD2 Protein: Development of Peptides for Immunomodulation DrugScoreCSDKnowledge-Based Scoring Function Derived from SmallMolecule Crystal Data with Superior Recognition Rate of Near-Native LigandPoses and Better Affinity Prediction

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