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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40
has manifestation of work	http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_19/m/print http://hub.abes.fr/acs/periodical/jmcmar/1997/volume_40/issue_19/m/web
Date Copyrighted	1997
Rights	Copyright © 1997 American Chemical Society
issue	19
Rights Holder	American Chemical Society
is Is Part Of of	Molecular Modeling and 3D-QSAR Studies on the Interaction Mechanism ofTripeptidyl Thrombin Inhibitors with Human α-Thrombin Medetomidine Analogs as α2-Adrenergic Ligands. 3. Synthesis and BiologicalEvaluation of a New Series of Medetomidine Analogs and Their PotentialBinding Interactions with α2-Adrenoceptors Involving a “Methyl Pocket” Synthesis and Structure−Activity Relationships of Potent Thrombin Inhibitors: Piperazides of 3-Amidinophenylalanine Structure−Activity Studies on Position 14 of Human α-Calcitonin Gene-RelatedPeptide Synthesis, Anti-HumanImmunodeficiency Virus andAnti-Hepatitis B Virus Activities of NovelOxaselenolane Nucleosides Synthesis and Binding Affinity of 2-Phenylimidazo[1,2-a]pyridine Derivativesfor both Central and Peripheral Benzodiazepine Receptors. A New Series ofHigh-Affinity and Selective Ligands for the Peripheral Type Inhibition of Melanoma Cell Binding to Type IV Collagen by Analogs of CellAdhesion Regulator Books of Interest Synthesis and Pharmacological Characterization ofAminocyclopentanetricarboxylic Acids: New Tools to Discriminate betweenMetabotropic Glutamate Receptor Subtypes Chemistry Today and Tomorrow: The Central,Useful, and Creactive Science By Ronald Breslow.American Chemical Society, Washington, DC. 1997. ix+ 134 pp. 18 × 25.5 cm. ISBN 0-8412-34640-4. $19.95. Evolution of the Dmt-Tic Pharmacophore: N-Terminal Methylated Derivativeswith Extraordinary δ Opioid Antagonist Activity Antitumor Agents. 178. Synthesis and Biological Evaluation of Substituted2-Aryl-1,8-naphthyridin-4(1H)-ones as Antitumor Agents That Inhibit TubulinPolymerization Fused Pyrrolo[2,3-c]carbazol-6-ones: Novel Immunostimulants That EnhanceHuman Interferon-γ Activity Dihydrobenzofuran Analogues of Hallucinogens. 4. Mescaline Derivatives Alkyl-Substituted Amino Acid Amides and Analogous Di- and Triamines: NewNon-Peptide G Protein Activators Conformationally Restricted Analogues of Trimethoprim: 2,6-Diamino-8-substituted Purines as Potential Dihydrofolate ReductaseInhibitors from Pneumocystis carinii and Toxoplasma gondii Curcumin Analogs with Altered Potencies against HIV-1 Integrase as Probes forBiochemical Mechanisms of Drug Action Ras Farnesyltransferase: A New Therapeutic Target 7-Spirobenzocyclohexyl Derivatives of Naltrexone, Oxymorphone, andHydromorphone as Selective Opioid Receptor Ligands Nonclassical 2,4-Diamino-5-aryl-6-ethylpyrimidine Antifolates: Activity asInhibitors of Dihydrofolate Reductase from Pneumocystis carinii andToxoplasma gondii and as Antitumor Agents Synthesis and Study of Thiocarbonate Derivatives of Choline as PotentialInhibitors of Acetylcholinesterase Conformational Studies of RS-66271, an Analog of ParathyroidHormone-Related Protein with Pronounced Bone Anabolic Activity

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