Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hideaki Tohjo"'
Publikováno v:
Biomedical Research. 18:465-469
Autor:
Hiroshi Sano, Hideaki Tohjo, Hiroshi Sato, Yoshiharu Katami, Eijiro Tagashira, Sachiko Yatsu, Yoshio Esumi, Tetsuyoshi Yokoshima, Seiji Toyama
Publikováno v:
Drug Metabolism and Pharmacokinetics. 7:461-476
The absorption, distribution, metabolism and excretion of 14C-nizatidine were studied after a single oral or intravenous administration of 5 mg/kg to rats.1. The blood levels of radioactivity reached a maximum concentration at 30 min after oral admin
Autor:
Matsuo Takaichi, Sadao Aoyama, Kenji Mizojiri, Naoko Saito, Shinya Hanawa, Kazuo Kamata, Koichi Sugeno, Hideaki Tohjo, Yoshio Esumi
Publikováno v:
Drug Metabolism and Pharmacokinetics. 3:83-99
The metabolism of 14C-S-3460 in rats, rabbits and mice was studied after subcutaneous administration at dose of 0.5 mg/kg. Plasma protein binding was also determined. 1. Plasma metabolites. The main metabolite was 21-hydroxy compound ((2)) and unchan
Autor:
Hiroshi SANO, Hiroshi SATO, Seiji TOYAMA, Eijiro TAGASHIRA, Yoshio ESUMI, Yoshiharu KATAMI, Hideaki TOHJO, Sachiko YATSU, Tetsuyoshi YOKOSHIMA
Publikováno v:
Drug Metabolism and Pharmacokinetics. 4:43-54
Autor:
Tetsuyoshi Yokoshima, Matsuo Takaichi, Yoshio Esumi, Kenji Mizojiri, Hideaki Tohjo, Koichi Sugeno
Publikováno v:
Drug Metabolism and Pharmacokinetics. 2:229-235
Transfer of 14C-dilevalol (Sch-19927) into the fetus and milk were studied following oral administration to pregnant or lactating rats at the dose level of 30 mg/kg. 1. On day 12 of gestation, the radioactivity in the fetus was lower than that in the
Autor:
Matsuo Takaichi, Yoshio Esumi, Hideaki Tohjo, Koichi Sugeno, Tetsuyoshi Yokoshima, Kenji Mizojiri
Publikováno v:
Drug Metabolism and Pharmacokinetics. 2:217-227
Autor:
Tetsuyoshi Yokoshima, Koichi Sugeno, Yoshio Esumi, Hideaki Tohjo, Matsuo Takaichi, Kenji Mizojiri
Publikováno v:
Drug Metabolism and Pharmacokinetics. 2:237-246
The absorption, metabolism and excretion of 14C-dilevalol (Sch-19927) were studied following a single or a 10 day period of daily oral administration to dogs at 30 mg/kg. 1. The plasma levels of radioactivity reached a peak level (15.22 μg equivalen
Autor:
Hiroshi SANO, Hiroshi SATO, Seiji TOYAMA, Eijiro TAGASHIRA, Yoshio ESUMI, Yoshiharu KATAMI, Hideaki TOHJO, Sachiko YATSU, Tetsuyoshi YOKOSHIMA
Publikováno v:
Drug Metabolism and Pharmacokinetics. 4:31-42
Autor:
Hideaki Tohjo, Hiroshi Sano, Hiroshi Sato, Seiji Toyama, Eijiro Tagashira, Yoshiharu Katami, Tetsuyoshi Yokoshima, Yoshio Esumi, Sachiko Yatsu
Publikováno v:
Drug Metabolism and Pharmacokinetics. 4:55-62
The absorption, metabolism and excretion of 14C-nizatidine were studied after a single oral administration of 5 mg/kg to male dogs.1. The blood levels of radioactivity reached a peak level (1876 ng eq./ml) at 1 hr after administration and then declin