Search Results - "SASAHARA, Kunihiro"
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Stereoselective pharmacokinetics of RS-8359, a selective and reversible MAO-A inhibitor, by species-dependent drug-metabolizing enzymes
Published in Chirality (New York, N.Y.) (2005)“…RS‐8359, (±)‐4‐(4‐cyanoanilino)‐5,6‐dihydro‐7‐hydroxy‐7H‐cyclopenta[d]pyrimidine selectively and reversibly inhibits monoamine oxidase A (MAO‐A). After oral…”
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2
Temocaprilat, a novel angiotensin-converting enzyme inhibitor, is excreted in bile via an ATP-dependent active transporter (cMOAT) that is deficient in Eisai hyperbilirubinemic mutant rats (EHBR)
Published in The Journal of pharmacology and experimental therapeutics (01-03-1997)“…Temocapril x HCl (alpha-((2S,6R)-6-[(1S)-1-ethoxy-carbonyl-3-phenyl-propyl]amino-5-oxo-2- (2-thienyl)perhydro-1,4-thiazepin-4-yl)acetic acid hydrochloride) is…”
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3
Pharmacokinetics of troglitazone, an antidiabetic agent: prediction of in vivo stereoselective sulfation and glucuronidation from in vitro data
Published in The Journal of pharmacology and experimental therapeutics (01-03-1997)“…Sulfation and glucuronidation, the major routes of metabolism of troglitazone, an antidiabetic agent, were examined in vitro using hepatic cytosol and…”
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4
An automated method for the simultaneous determination of pravastatin and its main metabolite in human plasma by high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry
Published in Biomedical chromatography (01-09-1998)“…A new method for the determination of pravastatin, a potent inhibitor of 3‐hydroxy‐3‐methylglutaryl coenzyme A (HMG‐CoA) reductase, and its main metabolite…”
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5
Trandolaprilat, an Angiotensin-Converting Enzyme Inhibitor, Is Not Excreted in Bile via an ATP-Dependent Active Transporter (cMOAT)
Published in Hypertension Research (01-05-2001)“…Trandolapril is the prodrug of an angiotensin-converting enzyme (ACE) inhibitor. It has been proposed that its active metabolite, trandolaprilat, is mainly…”
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6
Influence of modes of ACNU administration on tissue and blood drug concentration in malignant brain tumors
Published in Journal of neurosurgery (01-03-1987)“…The water-soluble nitrosourea compound ACNU is also lipid-soluble at normal physiological pH levels. It lacks toxic effects on vision that nitrosoureas…”
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7
Pain relief model for a COX‐2 inhibitor in patients with postoperative dental pain
Published in British journal of clinical pharmacology (01-07-2008)“…WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • Modelling and simulation are being increasingly used to support decision‐making in new drug development. • Novel…”
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Studies on Orally Active Cephalosporin Esters. II. : Chemical Stability of Pivaloyloxymethyl Esters in Phosphate Buffer Solution
Published in Chemical & pharmaceutical bulletin (1989)“…The degradation kinetics of pivaloyloxymethyl (POM) esters of cephalosporins in phosphate buffer solution (pH6-8) were investigated. The degradation of the…”
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9
Improvement of Bioavailability of Poorly Intestinally Absorbed Drugs from Medium-Chain Glyceride Base. Enhancement of the Rectal Absorption of Cefmetazole Sodium in Rabbits
Published in Chemical & pharmaceutical bulletin (01-01-1984)“…Medium-chain glyceride (MCG) enhanced the bioavailability of cefmetazole sodium, a watersoluble β-lactam antibiotic, after rectal administration to rabbits…”
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10
Prediction of the human pharmacokinetics of troglitazone, a new and extensively metabolized antidiabetic agent, after oral administration, with an animal scale-up approach
Published in The Journal of pharmacology and experimental therapeutics (01-06-1996)“…We have attempted to predict the human pharmacokinetics of troglitazone after oral administration based on animal data. Troglitazone is a new antidiabetic…”
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11
Sites of Action of CS-722, a Newly Synthesized Centrally Acting Muscle Relaxant
Published in Japanese Journal of Pharmacology (1993)“…Sites of the muscle relaxant action of CS-722 were investigated in rats. Doses injected intra-4th ventricularly (i.c.v.) or intrathecally (i.t.) were…”
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12
Sites of action of CS-722, a newly synthesized centrally acting muscle relaxant
Published in Japanese Journal of Pharmacology (1994)“…Sites of the muscle relaxant action of CS-722 were investigated in rats. Doses injected intra-4th ventricularly (i.c.v.) or intrathecally (i.t.) were…”
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13
Assessment of pharmacological effects and concentrations of RS-8359 on same rats by microdialysis
Published in Japanese Journal of Pharmacology (1994)“…RS-8359, which is under development as an anti-depressant, is a specific inhibitor of A-form monoamine oxidase (MAO-A). Dose-dependent increases in the…”
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14
HIGH-PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR DETERMINING THE CS-807 CONCENTRATION IN BODY FLUIDS
Published in CHEMOTHERAPY (1988)“…The following results were obtained by high-performance liquid chromatography (HPLC) of R-3763, the active metabolite of CS-807, in human serum and urine. 1)…”
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15
Improvement of bioavailability of poorly absorbed drugs. IV. Mechanism of the promoting effect of medium chain glyceride on the rectal absorption of water soluble drugs
Published in Journal of pharmacobio-dynamics (1985)“…The mechanisms of the promoting effect of medium chain glyceride (MCG) containing glyceryl mono-, di- and tri-caprylate on rectal absorption of water soluble…”
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16
Improvement of bioavailability of poorly absorbed drugs. I. Effect of medium chain glyceride base on the rectal absorption of cefmetazole sodium in rats
Published in Journal of pharmacobio-dynamics (01-11-1984)“…The effect of medium chain glyceride on the rectal absorption of cefmetazole sodium is investigated using an in situ experiment in rats. Each glyceride…”
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17
Improvement of bioavailability of poorly absorbed drugs. V. Effect of surfactants on the promoting effect of medium chain glyceride for the rectal absorption of beta-lactam antibiotics in rats and dogs
Published in Journal of pharmacobio-dynamics (1985)“…The promoting effects of medium chain glyceride (MCG) on the rectal absorption of beta-lactam antibiotics were compared among various experimental animals…”
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18
PHASE I CLINICAL STUDY OF CS-807, A NEW ORAL CEPHALOSPORIN
Published in CHEMOTHERAPY (1988)“…CS-807, a new cephalosporin for oral administration, is metabolized to an active metabolite (R-3763) by nonspecific esterase in the gut wall. R-3763 has been…”
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19
Studies on the Metabolism of Oxazolam. I. Distribution and Excretion Studies
Published in Chemical & pharmaceutical bulletin (1971)“…The distribution of orally and intravenously administered 14C-oxazolam was studied in mice by means of whole-body autoradiography and in rats by scintillation…”
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20
Improvement of bioavailability of poorly absorbed drugs. II. Effect of medium chain glyceride base on the intestinal absorption of cefmetazole sodium in rats and dogs
Published in Journal of pharmacobio-dynamics (1985)“…The effect of medium chain glyceride (MCG) on the intestinal absorption of cefmetazole sodium (CMZ) was investigated in rats and dogs. In rats, MCG containing…”
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