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Development of Potent Inhibitors of Botulinum Neurotoxin Type B
Design, Synthesis, and Crystal Structure of Selective 2-Pyridone Tissue FactorVIIa Inhibitors
Human β-Secretase (BACE) and BACE Inhibitors
Burger's Medicinal Chemistry and Drug Discovery. Sixth Edition. Volumes 1−6. Edited by D. J.Abraham. Wiley-Interscience, Hoboken, NJ. 2003. 18 ×26 cm. Vol. 1: xv + 932 pp; ISBN 0-471-27090-3. Vol.2: xv + 808 pp; ISBN 0-471-37028-2. Vol. 3: xv + 880pp; ISBN 0- 471-37029-0. Vol. 4: xiv + 702 pp; ISBN0-471-37030-4. Vol. 5: xv + 1084 pp; ISBN 0-471-37031-2. Vol. 6: xiv + 1084 pp; ISBN 0471-27401-1. $2100.00.
Inhibition of Human Immunodeficiency Virus Reverse Transcriptase bySynadenol Triphosphate and Its E-Isomer
Thienyl and Phenyl α-HalomethylKetones: New Inhibitors of GlycogenSynthase Kinase (GSK-3β) from a Libraryof Compound Searching
Nonpeptide αvβ3 Antagonists. 8. In Vitro and in Vivo Evaluation of a Potent αvβ3Antagonist for the Prevention and Treatment of Osteoporosis
Inclusion Complexation andSolubilization of Paclitaxel by BridgedBis(β-cyclodextrin)s Containing aTetraethylenepentaamino Spacer
Synthesis and Antiprotozoal Activity of Aza-Analogues of Furamidine
Molecular Determinants of Steroid Inhibition for the Mouse ConstitutiveAndrostane Receptor
Adenosine Kinase Inhibitors. 3. Synthesis, SAR, and Antiinflammatory Activityof a Series of l-Lyxofuranosyl Nucleosides
Synthesis and Pharmacological Evaluation of 1-Oxo-2-(3-piperidyl)-1,2,3,4-tetrahydroisoquinolines and Related Analogues as a New Class of SpecificBradycardic Agents Possessing If Channel Inhibitory Activity
Design and Synthesis of 4-Azaindoles as Inhibitors of p38 MAP Kinase
Thermal Denaturation: A Method to Rank Slow Binding, High-Affinity P38αMAP Kinase Inhibitors
Finding Discriminating Structural Features by Reassembling Common BuildingBlocks
Kinases, Homology Models, and High Throughput Docking
Taxus: The Genus Taxus. Medicinal and AromaticPlantsIndustrial Profiles. Volume 32 Edited byHideji Itokawa and Kuo-Hsiung Lee. Taylor & Francis,London and New York. 2003. xiii + 456 pp. 18 × 25.5cm. ISBN 0-415-29837-7. $145.00.
Azasterols as Inhibitors of Sterol 24-Methyltransferase in Leishmania Speciesand Trypanosoma cruzi
Structure−Activity Relationships of the p38α MAP Kinase Inhibitor1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)naph-thalen-1-yl]urea (BIRB 796)
Potent Inhibition of NTPase/Helicase of the West Nile Virus by Ring-Expanded(“Fat”) Nucleoside Analogues
Receptor-Guided Alignment-Based Comparative 3D-QSAR Studies ofBenzylidene Malonitrile Tyrphostins as EGFR and HER-2 Kinase Inhibitors
Convergent Synthesis and Unexpected Ca2+-Mobilizing Activity of 8-SubstitutedAnalogues of Cyclic ADP-Carbocyclic-Ribose, a Stable Mimic of theCa2+-Mobilizing Second Messenger Cyclic ADP-Ribose
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