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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_4/m/print http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_4/m/web
Date Copyrighted	2004
Rights	Copyright © 2004 American Chemical Society
issue	4
Rights Holder	American Chemical Society
is Is Part Of of	Synthesis of Flexible Sulfur-Containing Heteroarotinoids That InduceApoptosis and Reactive Oxygen Species with Discrimination betweenMalignant and Benign Cells Ligand-Based Structural Hypotheses for Virtual Screening Computer-Aided Design, Synthesis, and Anti-HIV-1 Activity in Vitro of2-Alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as Novel Potent Non-Nucleoside Reverse Transcriptase Inhibitors, AlsoActive Against the Y181C Variant Formation of Water-Soluble Pincer Silver(I)−Carbene Complexes: A NovelAntimicrobial Agent Antitumor Agents. 3. Design, Synthesis, and Biological Evaluation of NewPyridoisoquinolindione and Dihydrothienoquinolindione Derivatives withPotent Cytotoxic Activity Phe-Gly Dipeptidomimetics Designed for the Di-/Tripeptide TransportersPEPT1 and PEPT2: Synthesis and Biological Investigations Discovery of a New Class of Anilinoquinazoline Inhibitors with High Affinityand Specificity for the Tyrosine Kinase Domain of c-Src Synthesis of a5-Methylindolyl-Containing MacrocycleThat Displays Ultrapotent Grb2 SH2Domain-Binding Affinity Explorations of Peptide and Oligonucleotide Binding Sites of Tyrosyl-DNAPhosphodiesterase Using Vanadate Complexes Conformer- and Alignment-Independent Model for Predicting StructurallyDiverse Competitive CYP2C9 Inhibitors Importance of Phenolic Address Groups in Opioid Kappa Receptor SelectiveAntagonists Design, Synthesis, and Biological Characterization of Metabolically StableSelective Androgen Receptor Modulators Inhibitors of Serine Proteases as Potential Therapeutic Agents: The Road fromThrombin to Tryptase to Cathepsin G Prediction of HIV-1 Integrase/Viral DNA Interactions in the Catalytic Domainby Fast Molecular Docking Novel Heteroarotinoids as Potential Antagonists of Mycobacteriumbovis BCG Inhibition of Adenosine Deaminase by Novel 5:7 Fused Heterocycles Containingthe Imidazo[4,5-e][1,2,4]triazepine Ring System: A Structure−ActivityRelationship Study In Vitro Structure−Activity Relationship and in Vivo Studies for a Novel Classof Cyclooxygenase-2 Inhibitors: 5-Aryl-2,2-dialkyl-4-phenyl-3(2H)furanoneDerivatives Synthesis of Mono- and Bisdihydrodipyridopyrazines and Assessment of TheirDNA Binding and Cytotoxic Properties Recognition of Privileged Structures by G-Protein Coupled Receptors Preparation, Properties, Reactions, and Adenosine Receptor Affinities ofSulfophenylxanthine Nitrophenyl Esters: Toward the Development of SulfonicAcid Prodrugs with Peroral Bioavailability Compendium of Organic Synthetic Methods.Volume 11 By Michael B. Smith. John Wiley & Sons,Hoboken, NJ. 2003. xx + 795 pp. 16 × 24 cm. ISBN0-471-25965-9. $225.00. Jatrophane Diterpenes as Modulators of Multidrug Resistance. Advances ofStructure−Activity Relationships and Discovery of the Potent LeadPepluanin A Prediction of Ligand Binding Affinity and Orientation of Xenoestrogens to theEstrogen Receptor by Molecular Dynamics Simulations and the LinearInteraction Energy Method Structural Basis for the Synthesis of Indirubins as Potent and SelectiveInhibitors of Glycogen Synthase Kinase-3 and Cyclin-Dependent Kinases Virtual Screening with Flexible Docking and COMBINE-Based Models.Application to a Series of Factor Xa Inhibitors Synthesis, SAR, Crystal Structure, and Biological Evaluation ofBenzoquinoliziniums as Activators of Wild-Type and Mutant Cystic FibrosisTransmembrane Conductance Regulator Channels Undersulfated and Glycol-Split Heparins Endowed with Antiangiogenic Activity 5-Fluorinated l-Lysine Analogues as Selective Induced Nitric Oxide SynthaseInhibitors Macrocyclic Polyamines Deplete Cellular ATP Levels and Inhibit Cell Growthin Human Prostate Cancer Cells A Selective AT2 Receptor Ligand with a γ-Turn-Like Mimetic Replacing theAmino Acid Residues 4−5 of Angiotensin II Effects of C2-Alkylation, N-Alkylation, and N,N‘-Dialkylation on the Stabilityand Estrogen Receptor Interaction of (4R,5S)/(4S,5R)-4,5-Bis(4-hydroxyphenyl)-2-imidazolines

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