Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Tetsuro Tamai"'
Autor:
Yoshifusa Abe MD, PhD, Hitomi Wakabayashi, Yasuha Ogawa, Ayano Machida, Mio Endo, Tetsuro Tamai MD, Shunsuke Sakurai MD, PhD, Satoshi Hibino MD, PhD, Takeshi Mikawa MD, Yoshitaka Watanabe MD, PhD, Kazuhisa Ugajin ICMT, Kunihiko Fukuchi MD, PhD, Kazuo Itabashi MD, PhD
Publikováno v:
Global Pediatric Health, Vol 3 (2016)
To validate the policy of administering cefazolin (CEZ) as a first-line antibiotic to children who are hospitalized with their first febrile urinary tract infection (UTI), we evaluated microbial susceptibility to CEZ and the efficacy of CEZ. The 75 e
Externí odkaz:
https://doaj.org/article/a0a3c16335ac4c3eb055596dc36e590f
Autor:
Shuhei Takahashi, Ryosuke Kusano, Akiho Ueda, Naoaki Hori, Chieko Kusano, Yu Kuramochi, Rena Okada, Yuiko Suzuki, Tetsuro Tamai
Publikováno v:
The Kitakanto Medical Journal. 71:199-201
Autor:
Atsutoshi Shiratori, Satoshi Hibino, Kazushige Dobashi, Yoshifusa Abe, Yoshitaka Watanabe, Shuichiro Watanabe, Satomi Nimura, Tsuneki Watanabe, Yuya Nakano, Katsumi Mizuno, Yasuko Nakano, Kaori Kamijo, Kazuo Itabashi, Tetsuro Tamai, Hirokazu Ikeda, Shunsuke Sakurai, Takaaki Takayanagi
Publikováno v:
Clinical and Experimental Nephrology
Background Serum adiponectin circulates in three multimeric isoforms: high-molecular-weight (HMW), middle-molecular-weight (MMW), and low-molecular-weight (LMW) isoforms. Potential change in the circulating adiponectin levels in patients with nephrot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262c437eb0f5eb98e27ebcd665a92bff
https://doi.org/10.21203/rs.3.rs-28091/v1
https://doi.org/10.21203/rs.3.rs-28091/v1
Autor:
Nobuyuki Tanaka, Akihito Hirabayashi, Masuo Akahane, Hideyuki Muranaka, Harunobu Mukaiyama, Takehiro Ishikawa, Satoshi Akahane, Tetsuro Tamai
Publikováno v:
Bioorganic & Medicinal Chemistry. 9:3265-3271
In a search for novel analogues of beta(3)-adrenoceptor (AR) agonists relaxing the bladder for treatment of urinary dysfunction, 2-[4-(2-[[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethyl]amino]ethyl)phenoxy]-2-methylpropionic acids (1a-e), into w
Autor:
Hideyuki Rasukasasu Azumino Muranaka, Satoshi Akahane, Harunobu Mukaiyama, Hiroshi Miyata, Masuo Akahane, Nobuyuki Tanaka, Akihito Hirabayashi, Tetsuro Tamai
Publikováno v:
Journal of Medicinal Chemistry. 44:1436-1445
With a novel assay using isolated ferret detrusor to estimate beta(3)-adrenoceptor agonistic activity, we found that a series of glycine derivatives of ritodrine, a beta(2)-adrenoceptor agonist, are potent beta(3)-adrenoceptor agonists, with excellen
Autor:
Tetsuro Tamai, Satsuki Mukaiyama, Kuniaki Tatsuta, Yuko Nozaki, Mitsuhiro Kinoshita, Masaya Nakata, Kazunobu Toshima
Publikováno v:
Journal of the American Chemical Society. 117:3717-3727
Publikováno v:
Bulletin of the Chemical Society of Japan. 67:3057-3066
The first total synthesis of AB3217-A has been achieved. The deacetylanisomycin unit, (3S,4S,5R)-3-benzyloxy-1-(benzyloxycarbonyl)-5-[(1R)-1-hydroxy-1-(4-methoxyphenyl)methyl]-4-(2-tetrahydropyranyloxy)pyrrolidine (18), was prepared from dimethyl L-t
Autor:
Yasuyuki Kurita, Takashi Inagaki, Tetsuro Tamai, Hiroki Gunji, Ryonosuke Yoshida, Kuniaki Tatsuta, Shozo Miura
Publikováno v:
Bulletin of the Chemical Society of Japan. 67:1701-1707
A Z-isomer (4) of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acid, which is the common acyl moiety of clinically useful cephem antibiotics, has been prepared from the aminoisoxazoles through the skeletal rearrangement in several routes.
Publikováno v:
Tetrahedron Letters. 35:3099-3102
The first total synthesis of AB3217-A, a novel anti-mite substance, has been achieved via intermolecular etherification and intramolecular glycosylation as the key steps for the formation of the nine-membered ring.
Autor:
Tetsuro Tamai, Shozo Miura, Ryonosuke Yoshida, Takashi Inagaki, Kuniaki Tatsuta, Hiroki Gunji
Publikováno v:
Tetrahedron Letters. 34:6423-6426
A Z -isomer of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acid, which is the common acyl moiety of clinically useful cephalosporins, has been prepared from the aminoisoxazols through the thiadiazol-acetate in two pathways.