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Merck Research Laboratories | 論文
- Investigation of high-throughput ultrafiltration for the determination of an unbound compound in human plasma using liquid chromatography and tandem mass spectrometry with electrospray ionization
- Terminology of Developmental Abnormalities in Common Laboratory Mammals : Version 1
- Bioconversion of Indene to cis(1S, 2R)Indandiol and trans(1R, 2R)Indandiol by Rhodococcus Species
- Potential efficacy of the oral histone deacetylase inhibitor vorinostat in a phase I trial in follicular and mantle cell lymphoma
- Phase I and pharmacokinetic study of vorinostat (suberoylanilide hydroxamic acid) in Japanese patients with solid tumors
- Quinoxapeptins: Novel Chromodepsipeptide Inhibitors of HIV-1 and HIV-2 Reverse Transcriptase
- Isolation and Insecticidal/Anthelmintic Activity of Xanthonol, a Novel Bis-xanthone, from a Non-sporulating Fungal species
- Isolation and Structures of Novel Fungal Metabolites as Chemokine Receptor (CCR2) Antagonists
- Isolation, Structure and HIV-1 Integrase Inhibitory Activity of Exophillic Acid, a Novel Fungal Metabolite from Exophiala pisciphila
- Discovery of an Angiotensin II Binding Inhibitor from a Cytospora sp. Using Semi-automated Screening Procedures
- The Discovery of Australifungin, a Novel Inhibitor of Sphinganine N-Acyltransferase from Sporormiella australis Producing Organism, Fermentation, Isolation, and Biological Activity
- Production of a Family of Kinase-inhibiting, Lactones from Fungal Fermentations
- Chiral Bio-Resolution of Racemic Indene Oxide by Fungal Epoxide Hydrolases
- Therapeutic effects of alendronate 35mg once weekly and 5mg once daily in Japanese patients with osteoporosis : a double-blind, randomized study
- Monoamine Oxidase Type B is Localized to Mitochondrial Outer Membranes in Mast Cells, Schwann Cells, Endothelial Cells and Fibroblasts of the Rat Tongue
- Viridiofungins, Novel Inhibitors of Sphingolipid Synthesis
- High-throughput sample preparation procedures for the quantitation of a new bone integrin α_νβ_3 antagonist in human plasma and urine using liquid chromatography-tandem mass spectrometry
- 製薬企業における粉砕技術開発
- Process Development for the Producton of the (S)-Acid Precursor of a Novel Elastase Inhibitor (L-694,458) through the Lipase-Catalyzed Kinetic Resolution of a β-Lactam Benzyl Ester
- Asymmetric Bioreduction of a Keto Ester to Its Corresponding (S)-Hydroxy Ester by Microbacterium sp. MB 5614
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