Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Shin, Takusagawa"'
Publikováno v:
European Journal of Drug Metabolism and Pharmacokinetics. 43:301-309
Mirabegron is cleared by multiple mechanisms, including drug-metabolizing enzymes. One of the most important clearance pathways is direct glucuronidation. In humans, M11 (O-glucuronide), M13 (carbamoyl-glucuronide), and M14 (N-glucuronide) have been
Publikováno v:
Clinical Therapeutics. 37:1031-1044
Purpose The objective of these studies was to evaluate the pharmacokinetic profile, safety, and tolerability of mirabegron, a β 3 -adrenoceptor agonist for the treatment of overactive bladder, including food effects (low- or high-fat meals) and sex,
Autor:
Virginie Kerbusch, Walter Krauwinkel, Selina Moy, Alan Marion, Donna Kowalski, Michael Roy, James Keirns, Taiji Sawamoto, Jennifer Lee, Marcel van Gelderen, John Meijer, Shin Takusagawa
Publikováno v:
Clinical Drug Investigation. 33:429-440
Mirabegron is a β3-adrenoceptor agonist for the treatment of overactive bladder. There has been little information published or presented about the involvement of cytochrome P450 (CYP) isoenzymes 3A and 2D6 in the metabolism of mirabegron in humans;
Autor:
Virginie Kerbusch, Yutaka Takahashi, Hiroyuki Nemoto, Fumihiko Ushigome, Takafumi Iwatsubo, Aiji Miyashita, Shin Takusagawa, Takashi Usui, Qun Li
Publikováno v:
Molecular Pharmaceutics. 10:1783-1794
Mirabegron, a weak-basic compound, is a potent and selective β3-adrenoceptor agonist for the treatment of overactive bladder. Mirabegron extended release formulation shows dose-dependent oral bioavailability in humans, which is likely attributable t
Autor:
Shin, Takusagawa, Fumihiko, Ushigome, Hiroyuki, Nemoto, Yutaka, Takahashi, Qun, Li, Virginie, Kerbusch, Aiji, Miyashita, Takafumi, Iwatsubo, Takashi, Usui
Publikováno v:
Molecular pharmaceutics. 10(5)
Mirabegron, a weak-basic compound, is a potent and selective β3-adrenoceptor agonist for the treatment of overactive bladder. Mirabegron extended release formulation shows dose-dependent oral bioavailability in humans, which is likely attributable t
Publikováno v:
Plant Science. 121:167-174
A cDNA library was constructed with poly(A) + RNA prepared from 10-day-old rice seedlings. We have isolated three nuclear genes, rpl 13, rpl 24 and rpl 28, that encode chloroplast ribosomal proteins L13, L24 and L28, respectively. Comparison with the
Autor:
Takafumi Iwatsubo, Shotaro Uehara, Aiji Miyashita, Kanako Yajima, Shin Takusagawa, Takashi Usui
Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 42(10)
1. Human cytochrome P450 (CYP) enzymes and esterases involved in the metabolism of mirabegron, a potent and selective human β(3)-adrenoceptor agonist intended for the treatment of overactive bladder, were identified in in vitro studies. 2. Incubatio
Autor:
Aiji Miyashita, Marloes Schaddelee, Katsuhiro Suzuki, Marcel van Gelderen, John Meijer, Takafumi Iwatsubo, Mitsuhiro Sekiguchi, Walter Krauwinkel, Masanori Nagata, Jan Jaap van Lier, Shin Takusagawa, Takashi Usui
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 40(4)
The mass balance and metabolite profiles of 2-(2-amino-1,3-thiazol-4-yl)-N-[4-(2-{[(2R)-2-hydroxy-2-phenylethyl]amino}ethyl)[U-(14)C]phenyl]acetamide ([(14)C]mirabegron, YM178), a β(3)-adrenoceptor agonist for the treatment of overactive bladder, we
Autor:
Raymond van Teijlingen, Shin Takusagawa, Takashi Usui, Marcel van Gelderen, Cas van den Beld, John Meijer
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
Mirabegron is being developed for the treatment of overactive bladder. To support the development of mirabegron, including pharmacokinetic studies, liquid chromatography/tandem mass spectrometry methods for mirabegron and eight metabolites (M5, M8, M
Autor:
Mikio Nakazono, Shin-ichi Arimura, Shoji Hatano, Shin Takusagawa, Atsushi Hirai, Nobuhiro Tsutsumi
Publikováno v:
FEBS letters. 450(3)
We have cloned a novel nuclear gene for a ribosomal protein of rice and Arabidopsis that is like the bacterial ribosomal protein S9. To determine the subcellular localization of the gene product, we fused the N-terminal region and green fluorescent p