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1997
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Copyright © 1997 American Chemical Society
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5
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Heteroaromatic Analogs of 1-[2-(Diphenylmethoxy)ethyl]- and1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazines (GBR12935 and GBR 12909) as High-Affinity Dopamine Reuptake Inhibitors
Design, Synthesis, and Antiviral Evaluation of 2-Substituted 4,5-Dichloro- and4,6-Dichloro-1-β-d-ribofuranosylbenzimidazoles as Potential Agents for HumanCytomegalovirus Infections
(E)- and (Z)-7-Arylidenenaltrexones: Synthesis and Opioid ReceptorRadioligand Displacement Assays
Synthesis and Biological Activities of (R)-5,6-Dihydro-N,N-dimethyl-4H-imidazo[4,5,1-ij]quinolin-5-amine and Its Metabolites
Synthesis and Antiviral Activity of Certain 5‘-Modified Analogs of2,5,6-Trichloro-1-(β-d-ribofuranosyl)benzimidazole
Highly Selective Aldose Reductase Inhibitors. 3. Structural Diversity of3-(Arylmethyl)-2,4,5-trioxoimidazolidine-1-acetic Acids
Probes for Narcotic Receptor Mediated Phenomena. 23. Synthesis, OpioidReceptor Binding, and Bioassay of the Highly Selective δ Agonist(+)-4-[(αR)-α-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]-N,N-diethylbenzamide (SNC 80) and Related Novel Nonpeptide δ OpioidReceptor Ligands
Synthesis and Antitumor Evaluation of New Thiazolo[5,4-b]quinolineDerivatives
Synthesis and Antiproliferative and Antiviral Activity ofCarbohydrate-Modified Pyrrolo[2,3-d]pyridazin-7-one Nucleosides
Three-Dimensional Quantitative Structure−Activity Relationship of MelatoninReceptor Ligands: A Comparative Molecular Field Analysis Study
Structure-Based Design of Substituted Diphenyl Sulfones and Sulfoxides asLipophilic Inhibitors of Thymidylate Synthase
Synthesis, Antiproliferative and Antiviral Activity of Imidazo[4,5-d]isothiazoleNucleosides as 5:5 Fused Analogs of Nebularine and 6-MethylpurineRibonucleoside
Progress in Medicinal Chemistry. Volume 1. Studies in Medicinal Chemistry Edited by M. IqbalChoudhary. Harwood Academic Publishers, Newark,NJ. 1996. xiv + 390 pp. 18 × 25.5 cm. ISBN 3-7186-5795-3. $150.00.
From Peptide to Non-Peptide. 3. Atropisomeric GPIIbIIIa AntagonistsContaining the 3,4-Dihydro-1H-1,4-benzodiazepine-2,5-dione Nucleus
6-(1H-Imidazol-1-yl)-7-nitro-2,3(1H,4H)-quinoxalinedione (YM90K) and Related Compounds: Structure−Activity Relationships for the AMPA-Type Non-NMDAReceptor
Structural Requirements for Binding of Anandamide-Type Compounds to theBrain Cannabinoid Receptor
Books of Interest
Structure-Based Design of New Constrained Cyclic Agonists of theCholecystokinin CCK-B Receptor
Design, Synthesis, and Antiviral Evaluation of2-Chloro-5,6-dihalo-1-β-d-ribofuranosylbenzimidazoles as Potential Agents forHuman Cytomegalovirus Infections
Structure−Activity Relationships of Alkyl- and Alkoxy-Substituted1,4-Dihydroquinoxaline-2,3-diones: Potent and Systemically Active Antagonistsfor the Glycine Site of the NMDA Receptor
4-Substituted-3-phenylquinolin-2(1H)-ones: Acidic and Nonacidic Glycine SiteN-Methyl-d-aspartate Antagonists with inVivo Activity
Synthesis and Evaluation of 6-(Dibromomethyl)-5-nitropyrimidines as PotentialAntitumor Agents
Nonsteroidal Anti-Inflammatory Drugs as Scaffolds for the Design of5-Lipoxygenase Inhibitors
Correlation of Antimalarial Activity of Artemisinin Derivatives with BindingAffinity with Ferroprotoporphyrin IX
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