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1997
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Copyright © 1997 American Chemical Society
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9
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Antimalarial Activity of New Dihydroartemisinin Derivatives. 7.4-(p-Substituted phenyl)-4(R or S)-[10(α or β)-dihydroartemisininoxy]butyricAcids1-6
Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class ofCyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib)
Studies of Pyrrolo[1,2-a]benzimidazolequinone DT-Diaphorase SubstrateActivity, Topoisomerase II Inhibition Activity, and DNA Reductive Alkylation
Pharmacological Options in the Treatment of Benign Prostatic Hyperplasia
Carbocyclic Oxetanocins Lacking the C-3‘ Methylene
Hypoxia-Selective Antitumor Agents. 15. Modification of Rate ofNitroreduction and Extent of Lysosomal Uptake by Polysubstitution of4-(Alkylamino)-5-nitroquinoline Bioreductive Drugs
Modeling, Chemistry, and Biology of the Benzolactam Analogues of IndolactamV (ILV). 2. Identification of the Binding Site of the Benzolactams in the CRD2Activator-Binding Domain of PKCδ and Discovery of an ILV Analogue ofImproved Isozyme Selectivity
Enantioselective Synthesis and Antiproliferative Properties of an IlmofosineAnalog, 2‘-(Trimethylammonio)ethyl 3-(Hexadecyloxy)-2-(methoxymethyl)propylPhosphate, on Epithelial Cancer Cell Growth
Quantitative Structure−Activity Relationships among Macrolide AntibacterialAgents: In Vitro and in Vivo Potency against Pasteurella multocida
Synthesis and Ligand Binding of Nortropane Derivatives: N-Substituted2β-Carbomethoxy-3β-(4‘-iodophenyl)nortropane andN-(3-Iodoprop-(2E)-enyl)-2β-carbomethoxy-3β-(3‘,4‘-disubstitutedphenyl)nortropane. New High-Affinity and Selective Compounds for theDopamine Transporter
Bioactivities and Secondary Structures of Constrained Analogues of HumanParathyroid Hormone: Cyclic Lactams of the Receptor Binding Region
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