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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_7/m/print http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_7/m/web
Date Copyrighted	2007
Rights	Copyright © 2007 American Chemical Society
issue	7
Rights Holder	American Chemical Society
is Is Part Of of	Inhibition of Secreted Phospholipase A2. 4-Glycerol Derivatives of4,5-Dihydro-3-(4-tetradecyloxybenzyl)-1,2,4-4H-oxadiazol-5-one with Broad Activities 1,4-Benzodiazepines as Inhibitors of Respiratory Syncytial Virus. The Identification of aClinical Candidate Ovarian Cancer Activity of Cyclic Amine and Thiaether Metal Complexes Design, Synthesis, and Evaluation of the Antiproliferative Activity of a Series of Novel FusedXanthenone Aminoderivatives in Human Breast Cancer Cells N-(3,3a,4,4a,5,5a,6,6a-Octahydro-1,3-dioxo-4,6-ethenocycloprop[f]isoindol-2-(1H)-yl)carboxamides: Identification of Novel Orthopoxvirus EgressInhibitors Analogues of Acifran: Agonists of the High andLow Affinity Niacin Receptors, GPR109a andGPR109b Modeling the Preferred Shapes of Polyamine TransporterLigands and Dihydromotuporamine-C Mimics: Shovel versusHoe. Stressin1-A, a Potent Corticotropin Releasing Factor Receptor 1 (CRF1)-Selective PeptideAgonist Structure−Activity Relationship Study To Understand the Estrogen Receptor-Dependent GeneActivation of Aryl- and Alkyl-Substituted 1H-Imidazoles Probing the Pharmacophore of Ginkgolides as Glycine Receptor Antagonists Self-Organizing Maps for Identification of New Inhibitors of P-Glycoprotein Novel N-Substituted Indol-3-ylglyoxylamides Probing the LDi and L1/L2 Lipophilic Regions ofthe Benzodiazepine Receptor Site in Search for Subtype-Selective Ligands Peripheral and Axial Substitution of Phthalocyanines with Solketal Groups: Synthesis and InVitro Evaluation for Photodynamic Therapy Synthesis, Critical Micelle Concentrations, and Antimycobacterial Properties of Homologous,Dendritic Amphiphiles. Probing Intrinsic Activity and the “Cutoff” Effect Probing the Anticancer Activity of Nucleoside Analogues: A QSAR Model Approach Using anInternally Consistent Training Set Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 SelectiveAntagonists (Part 2) Structural and Functional Basis of Cyclooxygenase Inhibition Synthesis and Pharmacological Characterization of N3-Substituted Willardiine Derivatives: Role of the Substituent at the 5-Position of the Uracil Ring in the Development of Highly Potentand Selective GLUK5 Kainate Receptor Antagonists Identification and Synthesis of a Novel Selective Partial PPARδ Agonist with Full Efficacy onLipid Metabolism In Vitro and In Vivo Driving Forces in the Delivery of Penetratin Conjugated G Protein Fragment Stabilization of G-Quadruplex DNA and Down-Regulation of Oncogene c-myc by QuindolineDerivatives Synthetic Anticancer Vaccine Candidates: Rational Design of Antigenic Peptide Mimetics ThatActivate Tumor-Specific T-Cells New Drug Discovery & Development. By Daniel Lednicer.John Wiley & Sons, Inc., Hoboken, New Jersey. 2007. xii +190 pp. 16 × 24 cm. ISBN-10 0-470-00750-8. $89.95. Quinols As Novel Therapeutic Agents. 7. Synthesis of Antitumor4-[1-(Arylsulfonyl-1H-indol-2-yl)]-4-hydroxycyclohexa-2,5-dien-1-ones by Sonogashira Reactions http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_7/101021jm068038v/w NO-Donor COX-2 Inhibitors. New Nitrooxy-Substituted 1,5-Diarylimidazoles Endowed withCOX-2 Inhibitory and Vasodilator Properties Discovery of Diaryl Imidazolidin-2-one Derivatives, a Novel Class of Muscarinic M3 SelectiveAntagonists (Part 1) Structure-Based Design, Synthesis, and Biological Evaluation of Potent and SelectiveMacrocyclic Checkpoint Kinase 1 Inhibitors Enzymatically Activated cycloSal-d4T-monophosphates: The Third Generation ofcycloSal-Pronucleotides Synthesis and Biological Evaluation ofDihydromotuporamine Derivatives in Cells Containing ActivePolyamine Transporters. (Aryloxyacetylamino)benzoic Acid Analogues: A New Class of Hypoxia-Inducible Factor-1Inhibitors Discovery of N-(4-(3-Amino-1H-indazol-4-yl)phenyl)-N‘-(2-fluoro-5-methylphenyl)urea(ABT-869), a 3-Aminoindazole-Based Orally Active Multitargeted Receptor Tyrosine KinaseInhibitor Synthesis and Anti-Cancer Activity of C-Ring-Functionalized Prodigiosin Analogues Characterizing the 1,4-Dihydropyridines Binding Interactions in the L-Type Ca2+ Channel: Model Construction and Docking Calculations Factor Xa Inhibitors: S1 Binding Interactions of a Series ofN-{(3S)-1-[(1S)-1-Methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}sulfonamides Synthesis and Biological Evaluation of Selective Aromatase Expression Regulators in BreastCancer Cells Carbonic Anhydrase Inhibitors: Inhibition of Isozymes I, II, and IX with Triazole-LinkedO-Glycosides of Benzene Sulfonamides Synthesis of a New Class of Druglike Angiotensin II C-Terminal Mimics with Affinity for theAT2 Receptor

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