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1997
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Copyright © 1997 American Chemical Society
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2
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Identification of High-Potency Neuropeptide Y Analogues through SystematicLactamization
Cyclic Urea Amides: HIV-1 Protease Inhibitors with Low Nanomolar Potencyagainst both Wild Type and Protease Inhibitor Resistant Mutants of HIV
Synthesis and Inhibition Studies of Sulfur-Substituted Squalene OxideAnalogues as Mechanism-Based Inhibitors of 2,3-Oxidosqualene−LanosterolCyclase
Camptothecin and Minor-Groove Binder Hybrid Molecules: Synthesis,Inhibition of Topoisomerase I, and Anticancer Cytotoxicity in Vitro
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Structure−Activity Relationships of Selective Estrogen Receptor Modulators: Modifications to the 2-Arylbenzothiophene Core of Raloxifene
Chlorogenic Acid and Synthetic Chlorogenic Acid Derivatives: Novel Inhibitorsof Hepatic Glucose-6-phosphate Translocase
Synthesis and Protein Kinase C Inhibitory Activities of Balanol Analogs withReplacement of the Perhydroazepine Moiety
Butitaxel Analogues: Synthesis and Structure−Activity Relationships
Expeditious Syntheses of Sugar-Modified Nucleosides and Collections ThereofExploiting Furan-, Pyrrole-, and Thiophene-Based Siloxy Dienes
Coumarin-Based Inhibitors of HIV Integrase
3-[[(4-Aryl-1-piperazinyl)alkyl]cyclohexyl]-1H-indoles as Dopamine D2 PartialAgonists and Autoreceptor Agonists
Structure−Activity Relationships of Cysteine-Lacking Pentapeptide DerivativesThat Inhibit ras Farnesyltransferase
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