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1998
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Copyright © 1998 American Chemical Society
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12
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Cyclic HIV Protease Inhibitors: Design and Synthesis of Orally Bioavailable,Pyrazole P2/P2‘ Cyclic Ureas with Improved Potency
New Alkenyldiarylmethanes with Enhanced Potencies as Anti-HIV AgentsWhich Act as Non-Nucleoside Reverse Transcriptase Inhibitors
Second Supplements to the Second Edition ofRodd's Chemistry of Carbon Compounds. VolumeIV: Heterocyclic Compounds. Part A: Three-,Four- and Five-Membered Monoheterocyclic Compounds Edited by M. Sainsbury. Elsevier, Amsterdam. 1997. xxvi + 704 pp. 15.5 × 23 cm. ISBN-0-444-827366. $457.00.
Structure−Activity Relationships of the 7-Substituents of5,4‘-Diamino-6,8,3‘-trifluoroflavone, a Potent Antitumor Agent
Supramolecular Chemistry of Anions Edited byAntonio Bianchi, Kristin Bowman-James, and EnriqueGarcia-Espana. Wiley-VCH, New York, NY. 1997. xiv+ 461 pp. ISBN 0-471-18622-8. $79.95.
Arylpiperazines with Serotonin-3 Antagonist Activity: A ComparativeMolecular Field Analysis
Design, Synthesis, and Biological Evaluation of a Second Generation ofPyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as Potent and Selective A2AAdenosine Receptor Antagonists
Antimalarial Cyclic Peroxy Ketals
Combinatorial Chemistry, Synthesis and Application Edited by S. R. Wilson and A. W. Czarnik. JohnWiley & Sons, Inc., New York. 1997. ix + 269 pp. 16× 24 cm. ISBN 0-471-12687. $69.95.
Selective Inhibitors of Monoamine Oxidase (MAO). 5., 1-SubstitutedPhenoxathiin Inhibitors Containing No Nitrogen That Inhibit MAO A byBinding It to a Hydrophobic Site
Development of Orally Active Oxytocin Antagonists: Studies on1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2-methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662)and Related Pyridines
Second Supplements to the Second Edition ofRodd's Chemistry of Carbon Compounds. VolumeIV: Heterocyclic Compounds. Parb B: Five-Membered Monoheterocyclic Compounds: Alkaloids, Dyes, Pigments Edited by M. Sainsbury.Elsevier, Amsterdam. 1997. xvi + 509 pp. 15.5 × 23cm. ISBN-0-444-827587. $324.25.
Specific and Irreversible Cyclopeptide Inhibitors of Dipeptidyl Peptidase IVActivity of the T-Cell Activation Antigen CD26
Pharmacologic Analysis of Drug−Receptor Interaction By Terry Kenakin. Lippincott-Raven Publishers, Philadelphia. 1997. xii + 491 pp. 16 × 24 cm.ISBN 0-397-51815-3. $99.00.
Does the Anti-Hepatitis B Virus Activity of (+)-5‘-Noraristeromycin Exist in Its4‘-Epimer and 4‘-Deoxygenated Derivatives?
6β-Acetoxynortropane: A Potent Muscarinic Agonist with Apparent Selectivitytoward M2-Receptors
[125I/127I/131I]Iodorhodamine: Synthesis, Cellular Localization, andBiodistribution in Athymic Mice Bearing Human Tumor Xenografts andComparison with [99mTc]Hexakis(2-methoxyisobutylisonitrile)
Substituted Naphthofurans as Hallucinogenic Phenethylamine−ErgolineHybrid Molecules with Unexpected Muscarinic Antagonist Activity
Emerging Therapeutic Targets. Volume 1 Editedby R. Anand, P. Smith, and P. Warne. Ashley Publications Ltd., London. 1997, ix + 281 pp. 21 × 29.5 cm.ISSN 1460-0412. $865.00.
Newly Synthesized l-Enantiomers of 3'-Fluoro-Modifiedβ-2'-Deoxyribonucleoside 5'-Triphosphates Inhibit Hepatitis B DNA PolymerasesBut Not the Five Cellular DNA Polymerases α, β, γ, δ, and ε Nor HIV-1 ReverseTranscriptase
Orally Active Benzamide Antipsychotic Agents with Affinity for Dopamine D2,Serotonin 5-HT1A, and Adrenergic α1 Receptors
Second Supplements to the Second Edition ofRodd's Chemistry of Carbon Compounds. VolumeIV: Heterocyclic Compounds. Part E: Six-Membered Monoheterocyclic Compounds with a Hetero Atom from Groups IV, VI or VII of the PeriodicTable Edited by M. Sainsbury. Elsevier, Amsterdam.1997. xiv + 692 pp. 15.5 × 23 cm. ISBN-0-444-827536.$447.75.
Novel Benzothiazolin-2-one and Benzoxazin-3-one Arylpiperazine Derivativeswith Mixed 5HT1A/D2 Affinity as Potential Atypical Antipsychotics
Vancomycin: Conformational Consequences of the Sugar Substituent
Structural Analysis of Thrombin Complexed with Potent InhibitorsIncorporating a Phenyl Group as a Peptide Mimetic and Aminopyridines asGuanidine Substitutes
Highly Selective Neurotoxins. Basic and ClinicalApplications Edited by R. M. Kostrzewa. HumanaPress, Towota, NJ. 1998. xii + 404 pp. 16 × 23.5 cm.ISBN 0-89603-465-8. $125.00.
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