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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_11/m/print http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_11/m/web
Date Copyrighted	2001
Rights	Copyright © 2001 American Chemical Society
issue	11
Rights Holder	American Chemical Society
is Is Part Of of	Diguanidino and “Reversed” Diamidino 2,5-Diarylfurans as AntimicrobialAgents Potent Reversible Inhibitors of the Protein Tyrosine Phosphatase CD45 QSAR and Molecular Modeling Studies of Baclofen Analogues as GABABAgonists. Insights into the Role of the Aromatic Moiety in GABAB Binding andActivation Antiplasmodial Activity and Cytotoxicity of Bis-, Tris-, and Tetraquinolineswith Linear or Cyclic Amino Linkers Design, Synthesis, and PreclinicalCharacterization of Novel, HighlySelective Indole Estrogens Homology Modeling Using Multiple Molecular Dynamics Simulations andDocking Studies of the Human Androgen Receptor Ligand Binding DomainBound to Testosterone and Nonsteroidal Ligands Design, Synthesis, and Biological Evaluation of Analogues of the AntitumorAgent, 2-{4-[(7-Chloro-2-quinoxalinyl)oxy]phenoxy}propionic Acid (XK469) Recent Developments in the Biology and Medicinal Chemistry of PotassiumChannel Modulators: Update from a Decade of Progress Stepwise Modulation of Neurokinin-3 and Neurokinin-2 Receptor Affinity andSelectivity in Quinoline Tachykinin Receptor Antagonists Ether Phospholipid-AZT Conjugates Possessing Anti-HIV and Antitumor CellActivity. Synthesis, Conformational Analysis, and Study of Their ThermalEffects on Membrane Bilayers Enantioselective Syntheses of Dopaminergic (R)- and(S)-Benzyltetrahydroisoquinolines Synthesis and Biological Evaluation of Purine-Containing Butenolides Structural Basis of Binding of High-Affinity Ligands to Protein Kinase C: Prediction of the Binding Modes through a New Molecular Dynamics Methodand Evaluation by Site-Directed Mutagenesis Development of a Pharmacophore Model for Histamine H3 ReceptorAntagonists, Using the Newly Developed Molecular Modeling Program SLATE Quinazolin-4-one α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid(AMPA) Receptor Antagonists: Structure−Activity Relationship of the C-2 SideChain Tether The Role of Sugar Residues in Molecular Recognition by Vancomycin Estradiol-16α-carboxylic Acid Esters as Locally Active Estrogens Phenanthroindolizidine Alkaloids as Cytotoxic Substances in a DanaidButterfly, Ideopsis similis, against Human Cancer Cells Discovery of Novel Aldose Reductase Inhibitors Using a ProteinStructure-Based Approach: 3D-Database Search Followed by Design andSynthesis Synthesis and Structure−Activity Relationships of Naphthamides as DopamineD3 Receptor Ligands

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