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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_22/m/print http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_22/m/web
Date Copyrighted	2006
Rights	Copyright © 2006 American Chemical Society
issue	22
Rights Holder	American Chemical Society
is Is Part Of of	Further Studies on Imidazo[4,5-b]pyridine AT1 Angiotensin II Receptor Antagonists. Effectsof the Transformation of the 4-Phenylquinoline Backbone into 4-Phenylisoquinolinone or1-Phenylindene Scaffolds Peptide Inhibitors of West Nile NS3 Protease: SAR Study of Tetrapeptide Aldehyde Inhibitors Discovery of ((4R,5S)-5-Amino-4-(2,4,5-trifluorophenyl)cyclohex-1-enyl)-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone(ABT-341), a Highly Potent, Selective, OrallyEfficacious, and Safe Dipeptidyl Peptidase IVInhibitor for the Treatment of Type 2 Diabetes Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the PotentAnti-HCV Agent 2‘-C-Methylcytidine Cyclic MrIA: A Stable and Potent Cyclic Conotoxin with a Novel Topological Fold thatTargets the Norepinephrine Transporter 3-Aminoquinazolinediones as a New Class ofAntibacterial Agents Demonstrating ExcellentAntibacterial Activity Against Wild-Type andMultidrug Resistant Organisms Optimization of Chromone-2-carboxamide Melanin Concentrating Hormone Receptor 1Antagonists: Assessment of Potency, Efficacy, and Cardiovascular Safety Discovery of [4-Amino-2-(1-methanesulfonylpiperidin-4-ylamino)pyrimidin-5-yl](2,3-difluoro-6-methoxyphenyl)methanone (R547), A Potent and Selective Cyclin-Dependent Kinase Inhibitorwith Significant in Vivo Antitumor Activity Ligand Affinities Predicted with the MM/PBSA Method: Dependence on the SimulationMethod and the Force Field Of Molecules and Humans Design and Synthesis of a Novel Photoaffinity Ligand for the Dopamine and SerotoninTransporters Based on 2β-Carbomethoxy-3β-biphenyltropane Structure−Function Correlation of Chloroquine and Analogues as Transgene ExpressionEnhancers in Nonviral Gene Delivery A Chimeric Ligand Approach Leading to Potent Antiprion Active Acridine Derivatives: Design, Synthesis, and Biological Investigations Prediction of Activation Energies for Hydrogen Abstraction by Cytochrome P450 Stereoselective Chemoenzymatic Synthesis of the Four Stereoisomers ofl-2-(2-Carboxycyclobutyl)glycine and Pharmacological Characterization at Human ExcitatoryAmino Acid Transporter Subtypes 1, 2, and 3 Dipyridyl Thiosemicarbazone Chelators with Potent and Selective Antitumor Activity FormIron Complexes with Redox Activity 4-Arylazo-3,5-diamino-1H-pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complexwith CDK2, Selectivity, and Cellular Effects N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methylpiperazin-1-yl)ethoxy]-5-(tetrahydro-2H-pyran-4-yloxy)quinazolin-4-amine, a Novel, Highly Selective,Orally Available, Dual-Specific c-Src/Abl Kinase Inhibitor Evaluation of 3-Carboxy-4(1H)-quinolones as Inhibitors of Human Protein Kinase CK2 Arylmethyloxyphenyl Derivatives: Small Molecules Displaying P-Glycoprotein Inhibition A Novel Class of Carbonic Anhydrase Inhibitors: Glycoconjugate Benzene SulfonamidesPrepared by “Click-Tailing”

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