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Biopharmaceutical and Pharmacokinetic Research Laboratories, Fujisawa Pharmaceutical Co., Ltd. | 論文
- Interindividual Variability in 5-Fluorouracil Metabolism and Procainamide N-Acetylation in Human Liver Cytosol(Biochemistry/Molecular Biology)
- Identification of Cytochrome P450 Enzymes Involved in the Metabolism of FK228, a Potent Histone Deacetylase Inhibitor, in Human Liver Microsomes(Biopharmacy)
- Interindividual Variability in 2-Hydroxylation, 3-Sulfation, and 3-Glucuronidation of Ethynylestradiol in Human Liver(Biochemistry/Molecular Biology)
- Effect of Nilvadipine, a Dihydropyridine Calcium Antagonist, on Cytochrome P450 Activities in Human Hepatic Microsomes (Biochemistry/Molecular Biology)
- Effect of Cefixime and Cefdinir, Oral Cephalosporins, on Cytochrome P450 Activities in Human Hepatic Microsomes(Biochemistry/Molecular Biology)
- New SRM Data Dependent Exclusion (MS)^n Measurement for Structural Determination of Drug Metabolites Using LC/ESI/Ion Trap MS
- Stategy for Structure Elucidation of Drug Metabolites Derived from Protonated Molecules and (MS)^n Fragmentation of Zotepine, Tiaramide and their Metabolites
- Effect of Antifungal Drugs on Cytochrome P450 (CYP) 2C9, CYP2C19, and CYP3A4 Activities in Human Liver Microsomes(Biopharmacy)
- No Inhibition of Cytochrome P450 Activities in Human Liver Microsomes by Sulpiride, an Antipsychotic Drug(Biopharmacy)
- Tissue Distribution after Intravenous Dosing of Micafungin, an Antifungal Drug, to Rats(Biopharmacy)
- FK317, a Novel Substituted Dihydrobenzoxazine, Exhibits Potent Antitumor Activity against Human Tumor Xenografts in Nude Mice
- Evidence for Singlet Oxygen Involvement in Rat and Human Cytochrome P450-dependent Substrate Oxidations
- Quantitative Determination Method for Trace Amount of Penicillin Contaminants in Commercially Available Drug Product by HPLC Coupled with Tandem Mass Spectrometry
- Utility of Microtiter Plate Assays for Human Cytochrome P450 Inhibition Studies in Drug Discovery : Application of Simple Method for Detecting Quasi-irreversible and Irreversible Inhibitors
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