About: http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_18/w

Documentation

scienceplus.abes.fr version Bêta

scienceplus.abes.fr | explorer

À propos de : http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_18/w Goto Sponge NotDistinct Permalink

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_18/m/print http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_18/m/web
Date Copyrighted	2003
Rights	Copyright © 2003 American Chemical Society
issue	18
Rights Holder	American Chemical Society
is Is Part Of of	Synthesis and Pharmacological Evaluation of Potent and Highly Selective D3Receptor Ligands: Inhibition of Cocaine-Seeking Behavior and the Role ofDopamine D3/D2 Receptors Oxindole-Based Compounds Are Selective Inhibitors of Plasmodium falciparumCyclin Dependent Protein Kinases Influence of Phenyl Ring Disubstitution on Bisbenzimidazole andTerbenzimidazole Cytotoxicity: Synthesis and Biological Evaluation asRadioprotectors Synthesis, Biological Evaluation, and Receptor Docking Simulations of2-[(Acylamino)ethyl]-1,4-benzodiazepines as κ-Opioid Receptor AgonistsEndowed with Antinociceptive and Antiamnesic Activity Pyrazole Derivatives as Partial Agonists for the Nicotinic Acid Receptor Synthesis and Biological Evaluation of Novel Flavone-8-acetic Acid Derivativesas Reversible Inhibitors of Aminopeptidase N/CD13 N6-SubstitutedD-4‘-Thioadenosine-5‘-methyluronamides: Potent and Selective Agonists at theHuman A3 Adenosine Receptor Novel Pyrone Side Tetracyclic Psoralen Derivatives: Synthesis andPhotobiological Evaluation Potent, Small-Molecule Inhibitors of Human Mast Cell Tryptase. AntiasthmaticAction of a Dipeptide-Based Transition-State Analogue Containing aBenzothiazole Ketone Fluorine Substitution Can Block CYP3A4Metabolism-Dependent Inhibition: Identification of (S)-N-[1-(4-Fluoro-3-morpholin-4-ylphenyl)ethyl]-3-(4-fluorophenyl)acrylamide as an OrallyBioavailable KCNQ2 Opener Devoid ofCYP3A4 Metabolism-DependentInhibition Structure-Based Design of a MacrocyclicInhibitor for Peptide Deformylase Binding of Tetrahydrocarboline Derivatives at Human 5-HT5A Receptors Books of Interest N-(ω-(4-(2-Methoxyphenyl)piperazin-1-yl)alkyl)carboxamides as Dopamine D2and D3 Receptor Ligands A Novel Approach of Water-SolublePaclitaxel Prodrug with No Auxiliaryand No Byproduct: Design and Synthesisof Isotaxel Thalidomide Metabolites and Analogues. 3. Synthesis and AntiangiogenicActivity of the Teratogenic and TNFα-Modulatory Thalidomide Analogue2-(2,6-Dioxopiperidine-3-yl)phthalimidine Stereospecific Synthesis of 5-Substituted 2-Bisarylthiocyclopentane CarboxylicAcids as Specific Matrix Metalloproteinase Inhibitors 3‘-C-Branched-Chain-Substituted Nucleosides and Nucleotides as PotentInhibitors of Mycobacterium tuberculosis Thymidine Monophosphate Kinase DNA Binding Ligands Targeting Drug-Resistant Bacteria: Structure, Activity,and Pharmacology A New Class of Diamine-Based Human Histamine H3 Receptor Antagonists: 4-(Aminoalkoxy)benzylamines

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata