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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_25/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_25/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	25
Rights Holder	American Chemical Society
is Is Part Of of	Novel Tropane-Based Irreversible Ligands for the Dopamine Transporter New Antimitotic Agents with Activity in Multi-Drug-Resistant Cell Lines and inVivo Efficacy in Murine Tumor Models O-Phosphonatomethylcholine, Its Analogues, Alkyl Esters, and Their BiologicalActivity Systematic Structure-Based Design and Stereoselective Synthesis of NovelMultisubstituted Cyclopentane Derivatives with Potent Antiinfluenza Activity [1,2,4]Triazino[4,3-a]benzimidazole Acetic Acid Derivatives: A New Class ofSelective Aldose Reductase Inhibitors Antimalarial Alkoxylated and Hydroxylated Chalones: Structure−ActivityRelationship Analysis Synthesis and Biological Studies of Novel Nucleoside PhosphoramidateProdrugs Design, Synthesis, and Biological Activity of a Novel Non-Cisplatin-typePlatinum−Acridine Pharmacophore trans-4-[4-(Methoxyphenyl)cyclohexyl]-1-arylpiperazines: A New Class of Potentand Selective 5-HT1A Receptor Ligands as Conformationally ConstrainedAnalogues of 4-[3-(5-Methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)propyl]-1-arylpiperazines Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design,Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis Discovery of Small-Molecule Inhibitors of Bcl-2 through Structure-BasedComputer Screening 3-(Arylacetylamino)-N-methylbenzamides: A Novel Class of SelectiveAnti-Helicobacter pylori Agents Nonsteroidal Selective Glucocorticoid Modulators: the Effect of C-5 AlkylSubstitution on the Transcriptional Activation/Repression Profile of2,5-Dihydro-10-methoxy-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolines Cheminformatic Models To Predict Binding Affinities to Human SerumAlbumin Free Energy Component Analysis for Drug Design: A Case Study of HIV-1Protease−Inhibitor Binding Synthesis and Structure−Activity Relationships ofN-(1-Benzylpiperidin-4-yl)arylacetamide Analogues as Potent σ1 ReceptorLigands Discovery of Novel p-Arylthio Cinnamides as Antagonists of LeukocyteFunction-Associated Antigen-1/Intercellular Adhesion Molecule-1 Interaction. 4.Structure−Activity Relationship of Substituents on the Benzene Ring of theCinnamide Conformationally Constrained Analoguesof Diacylglycerol. 18. The Incorporationof a Hydroxamate Moiety intoDiacylglycerol-Lactones ReducesLipophilicity and Helps Discriminatebetween sn-1 and sn-2 Binding Modes toProtein Kinase C (PK-C). Implications forIsozyme Specificity

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