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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_5/m/print http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_5/m/web
Date Copyrighted	2000
Rights	Copyright © 2000 American Chemical Society
issue	5
Rights Holder	American Chemical Society
is Is Part Of of	1,2-Dibenzamidobenzene Inhibitors of Human Factor Xa Inhibition of Grb2 SH2 Domain Binding by Non-Phosphate-Containing Ligands.2. 4-(2-Malonyl)phenylalanine as a Potent Phosphotyrosyl Mimetic Monocyclic l-Nucleosides with Type 1 Cytokine-Inducing Activity Design, Synthesis, and Enzymatic Evaluation of Multisubstrate AnalogueInhibitors of Escherichia coli Thymidine Phosphorylase Consensus Bioactive Conformation of Cyclic GnRH Antagonists Defined byNMR and Molecular Modeling Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked(Azolylphenyl)oxazolidinones with Expanded Activity Against the FastidiousGram-Negative Organisms Haemophilus influenzae and Moraxella catarrhalis 2-Substituted Tryptamines: Agents with Selectivity for 5-HT6 SerotoninReceptors 4-[5-Methyl-3-phenylisoxazol-4-yl]-benzenesulfonamide, Valdecoxib: APotent and Selective Inhibitor of COX-2 Design and Synthesis of 13,14-Dihydro Prostaglandin F1α Analogues as Potentand Selective Ligands for the Human FP Receptor Design of Potent Dicyclic (4−10/5−8) Gonadotropin Releasing Hormone (GnRH)Antagonists N-Terminal Dipeptides of d(−)-Penicillamine as Sequestration Agents forAcetaldehyde N2-Aroylanthranilamide Inhibitors of Human Factor Xa Synthesis of N-Substituted 4-(4-Hydroxyphenyl)piperidines,4-(4-Hydroxybenzyl)piperidines, and (±)-3-(4-Hydroxyphenyl)pyrrolidines: Selective Antagonists at the 1a/2B NMDA Receptor Subtype Novel 1,5-Diphenylpyrazole Nonnucleoside HIV-1 Reverse TranscriptaseInhibitors with Enhanced Activity versus the Delavirdine-Resistant P236LMutant: Lead Identification and SAR of 3- and 4-Substituted Derivatives Dual Function Glutamate-RelatedLigands: Discovery of a Novel, PotentInhibitor of Glutamate CarboxypeptidaseII Possessing mGluR3 Agonist Activity 1-(2-Nitrophenyl)thiosemicarbazides: ANovel Class of Potent, Orally ActiveNon-Peptide Antagonist for theBradykinin B2 Receptor Design of Potent Dicyclic (1−5/4−10) Gonadotropin Releasing Hormone (GnRH)Antagonists Design of Monocyclic (1−3) and Dicyclic (1−3/4−10) Gonadotropin ReleasingHormone (GnRH) Antagonists Synthesis, Biological Activity, and Molecular Modeling of Ribose-ModifiedDeoxyadenosine Bisphosphate Analogues as P2Y1 Receptor Ligands 5,6-Dihydropyran-2-ones Possessing Various Sulfonyl Functionalities: PotentNonpeptidic Inhibitors of HIV Protease New Azolidinediones as Inhibitors of Protein Tyrosine Phosphatase 1B withAntihyperglycemic Properties Selective ETA Antagonists. 5. Discovery and Structure−Activity Relationships ofPhenoxyphenylacetic Acid Derivatives Potent Anti-HIV (Type 1 and Type 2) Activity of Polyoxometalates: Structure−Activity Relationship and Mechanism of Action Structure-Based Design of Potent, Amidine-Derived Inhibitors of Factor Xa: Evaluation of Selectivity, Anticoagulant Activity, and Antithrombotic Activity Conformationally Constrained Analogues of Diacylglycerol (DAG). 16. HowMuch Structural Complexity Is Necessary for Recognition and High BindingAffinity to Protein Kinase C? α2 Adrenoceptor Agonists as PotentialAnalgesic Agents. 2. Discovery of4-(4-Imidazo)-1,3-dimethyl-6,7-dihydrothianaphthene as a High-Affinity Ligandfor the α2D Adrenergic Receptor

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