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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_25/m/print http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_25/m/web
Date Copyrighted	2003
Rights	Copyright © 2003 American Chemical Society
issue	25
Rights Holder	American Chemical Society
is Is Part Of of	1,2-Benzisoxazole Phosphorodiamidates as Novel Anticancer ProdrugsRequiring Bioreductive Activation Synthesis and Structure−Activity Relationship of Novel, Highly PotentMetharyl and Methcycloalkyl Cyclooxygenase-2 (COX-2) Selective Inhibitors Polyamine−Iron Chelator Conjugate Synthesis of a Prodrug Designed To Release Multiple Inhibitors of theEpidermal Growth Factor Receptor Tyrosine Kinase and an Alkylating Agent: A Novel Tumor Targeting Concept Guanidino N-Substituted and N,N-Disubstituted Derivatives of the κ-OpioidAntagonist GNTI Anticancer Activity of Phenolic Acids of Natural or Synthetic Origin: AStructure−Activity Study Synthesis, Comparative Photosensitizing Efficacy, Human Serum Albumin (SiteII) Binding Ability, and Intracellular Localization Characteristics of NovelBenzobacteriochlorins Derived from vic-Dihydroxybacteriochlorins Synthesis and Structure−Activity Relationships of ConformationallyConstrained Histamine H3 Receptor Agonists Carbonic Anhydrase Inhibitors: Inhibition of Transmembrane,Tumor-Associated Isozyme IX, and Cytosolic Isozymes I and II with AliphaticSulfamates Design, Synthesis, and Biological Activityof a Difluoro-Substituted,Conformationally Rigid VigabatrinAnalogue as a Potent γ-AminobutyricAcid Aminotransferase Inhibitor Analgesics. From Chemistry and Pharmacology toClinical Application Edited by H. Buschmann, T.Christoph, E. Friderichs, C. Maul, and B. Sundermann.Wiley-VCH, Weinheim, Germany. 2002. ix + 604 pp. 18× 25 cm. ISBN 3527304037. $185.00. An Alpha Helix Conformationally Restricted Peptide Is Recognized by CervicalCarcinoma Patients' Sera Synthesis and Biological Evaluation of 4-Arylcoumarin Analogues ofCombretastatins Molecular Basis of Neurotrophin−Receptor Interactions Pyrazole and Isoxazole Derivatives as New, Potent, and Selective20-Hydroxy-5,8,11,14-eicosatetraenoic Acid Synthase Inhibitors A Method for Designing Conformationally Restricted Analogues Based onAllylic Strain: Synthesis of a Novel Class of Noncompetitive NMDA ReceptorAntagonists Having the Acrylamide Structure Synthesis and Evaluation of ImidazoleAcetic Acid Inhibitors of ActivatedThrombin-Activatable FibrinolysisInhibitor as Novel Antithrombotics New Lupane Derived Compounds with Pro-Apoptotic Activity in Cancer Cells: Synthesis and Structure−Activity Relationships Synthesis and Evaluation of Nitroheterocyclic Carbamate Prodrugs for Usewith Nitroreductase-Mediated Gene-Directed Enzyme Prodrug Therapy Characterization of the 5-HT7 Receptor. Determination of the Pharmacophorefor 5-HT7 Receptor Agonism and CoMFA-Based Modeling of the Agonist BindingSite Nα-Imidazolylalkyl and Pyridylalkyl Derivatives of Histaprodifen: Synthesisand in Vitro Evaluation of Highly Potent Histamine H1-Receptor Agonists Molecular Model of the αIIbβ3 Integrin Application of the λ-Dynamics Method To Evaluate the Relative Binding FreeEnergies of Inhibitors to HCV Protease Neurosteroid Analogues. 9. Conformationally Constrained Pregnanes: Structure−Activity Studies of 13,24-Cyclo-18,21-dinorcholane Analogues of theGABA Modulatory and Anesthetic Steroids (3α,5α)- and(3α,5β)-3-Hydroxypregnan-20-one Syntheses and Binding Studies of New [(Aryl)(aryloxy)methyl]piperidineDerivatives and Related Compounds as Potential Antidepressant Drugs withHigh Affinity for Serotonin (5-HT) and Norepinephrine (NE) Transporters Discovery of 1-(2-Aminomethylphenyl)-3-trifluoromethyl-N-[3-fluoro-2‘-(aminosulfonyl)[1,1‘-biphenyl)]-4-yl]-1H-pyrazole-5-carboxyamide(DPC602), a Potent, Selective, and Orally Bioavailable Factor Xa Inhibitor A New Class of Potent Vascular Endothelial Growth Factor Receptor TyrosineKinase Inhibitors: Structure−Activity Relationships for a Series of9-Alkoxymethyl-12-(3-hydroxypropyl)indeno[2,1-a]pyrrolo[3,4-c]carbazole-5-onesand the Identification of CEP-5214 and Its Dimethylglycine Ester ProdrugClinical Candidate CEP-7055

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