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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_23/m/print http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_23/m/web
Date Copyrighted	2003
Rights	Copyright © 2003 American Chemical Society
issue	23
Rights Holder	American Chemical Society
is Is Part Of of	Conformational Study of Lipophilic Ligands in Phospholipid Model MembraneSystems by Solution NMR Multidrug Resistance Reversal Agents Design, Synthesis, and Biological Evaluation of6-Substituted-3-(4-methanesulfonylphenyl)-4-phenylpyran-2-ones: A Novel Classof Diarylheterocyclic Selective Cyclooxygenase-2 Inhibitors 5-Substituted-2,4-diamino-6-[2-(phosphonomethoxy)ethoxy]pyrimidinesAcyclicNucleoside Phosphonate Analogues with Antiviral Activity Dissociation of Antibacterial andHemolytic Activities of an AmphipathicPeptide Antibiotic Synthesis and Biological Evaluation of2‘-Methyl Taxoids Derived from BaccatinIII and 14β-OH-Baccatin III1,14-Carbonate Synthesis, Characterization, and Biological Properties of 8-Azido- and8-Amino-Substituted 2‘,5‘-Oligoadenylates Multivalent Antibiotics via Metal Complexes: Potent Divalent Vancomycinsagainst Vancomycin-Resistant Enterococci Design, Synthesis, and SAR of Potent and Selective Dipeptide-DerivedInhibitors for Dipeptidyl Peptidases Nitroaryl Phosphoramides as NovelProdrugs for E. coli NitroreductaseActivation in Enzyme Prodrug Therapy Synthesis and Biological Evaluation of 5-Substituted Derivatives of the PotentAntiherpes Agent (north)-Methanocarbathymine Isoquine and Related Amodiaquine Analogues: A New Generation of Improved4-Aminoquinoline Antimalarials Prazosin-Related Compounds. Effect of Transforming thePiperazinylquinazoline Moiety into an Aminomethyltetrahydroacridine Systemon the Affinity for α1-Adrenoreceptors Structure−Activity Relationships of γ-MSH Analogues at the HumanMelanocortin MC3, MC4, and MC5 Receptors. Discovery of Highly SelectivehMC3R, hMC4R, and hMC5R Analogues Synthesis, Characterization, and in Vitro Antitumor Activity of OsteotropicDiam(m)ineplatinum(II) Complexes Bearing aN,N-Bis(phosphonomethyl)glycine Ligand Medicinal Plants of the World. Volume I: Chemical Constituents, Traditional and Modern Uses.Second Edition By Ivan A. Ross. Humana Press,Totawa, NJ. 2003. xv + 489 pp. 16.5 × 26 cm. ISBN1-58829-281-9. $99.50. Estrogenic Potential of 2-Alkyl-4-(thio)chromenone 6-O-Sulfamates: PotentInhibitors of Human Steroid Sulfatase Poly(ethylene glycol) Transport Forms of Vancomycin: A Long-LivedContinuous Release Delivery System Design and Synthesis of trans-3-(2-(4-((3-(3-(5-Methyl-1,2,4-oxadiazolyl))-phenyl)carboxamido)cyclohexyl)ethyl)-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SB-414796): A Potent and Selective Dopamine D3Receptor Antagonist Three-Dimensional Quantitative Structure−Activity Relationship Analysis ofPropafenone-Type Multidrug Resistance Modulators: Influence of VariableSelection on Test Set Predictivity Modeling the Adenosine Receptors: Comparison of the Binding Domains of A2AAgonists and Antagonists 2-Substitution of Adenine Nucleotide Analogues Containing aBicyclo[3.1.0]hexane Ring System Locked in a Northern Conformation: Enhanced Potency as P2Y1 Receptor Antagonists Synthesis and Biological Evaluation of2,4-Diamino-6-(arylaminomethyl)pyrido[2,3-d]pyrimidines as Inhibitors ofPneumocystis carinii and Toxoplasma gondii Dihydrofolate Reductase and asAntiopportunistic Infection and Antitumor Agents CpG Oligonucleotides with Modified Termini and Nicked Dumbbell StructureShow Enhanced Immunostimulatory Activity Discovery of (Aryloxopropenyl)pyrrolylHydroxyamides as Selective Inhibitors ofClass IIa Histone Deacetylase HomologueHD1-A Potent and Selective Inhibitors of Platelet-Derived Growth Factor ReceptorPhosphorylation. 3. Replacement of Quinazoline Moiety and Improvement ofMetabolic Polymorphism of 4-[4-(N-Substituted(thio)carbamoyl)-1-piperazinyl]-6,7-dimethoxyquinazoline Derivatives Anti-Herpes Simplex Virus Activity of Substituted 1-Hydroxyacridones Large Dimeric Ligands with Favorable Pharmacokinetic Properties andPeroxisome Proliferator-Activated Receptor Agonist Activity in Vitro and inVivo A New Generation of N-Aryl-N‘-(1-alkyl-2-chloroethyl)ureas as MicrotubuleDisrupters: Synthesis, Antiproliferative Activity, and β-Tubulin AlkylationKinetics Synthesis, in Vitro Evaluation, and Intraocular Pressure Effects ofWater-Soluble Prodrugs of Endocannabinoid Noladin Ether Synthesis and Ca2+-Mobilizing Activity of Purine-Modified Mimics ofAdenophostin A: A Model for the Adenophostin−Ins(1,4,5)P3 ReceptorInteraction Molecular Docking Studies of Natural Cholinesterase-Inhibiting SteroidalAlkaloids from Sarcococca saligna Identification of a Potent and Selective5-HT6 Antagonist: One-Step Synthesis of(E)-3-(Benzenesulfonyl)-2-(methylsulfanyl)pyrido[1,2-a]pyrimidin-4-ylidenamine from2-(Benzenesulfonyl)-3,3-bis(methylsulfanyl)acrylonitrile

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