Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Mamoru Fujioka"'
Autor:
Shinichiro Nakamura, Hiroko Iijima, Yusuke Shibata, Yutaka Watanuki, Sadanobu Ogawa, Takashi Kumada, Hironori Ichikawa, Mamoru Fujioka, Saki Kataoka, Satoshi Yasuda, Toshifumi Tada, Shinichi Hashinokuchi, Kenji Takeshima, Naoya Fukuda, Kazuyuki Tsujii, Fumihiko Niwa, Hidenori Toyoda
Publikováno v:
Hepatology research : the official journal of the Japan Society of HepatologyReferences. 50(12)
AIM A new method has recently been developed for diagnosing hepatic steatosis based on attenuation measurement using ultrasound. We investigated the ability of attenuation imaging (ATI) to detect steatosis that was identified by proton density fat fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::366dee8dad260f8916aa9f39dd4a8360
https://pubmed.ncbi.nlm.nih.gov/32876367
https://pubmed.ncbi.nlm.nih.gov/32876367
Autor:
Yayoi Shihahara, Yoshihiko Okamoto, Marie T. Mooney, Shinnichiro Suzuki, Kyoko Yamamoto, Mamoru Fujioka, Shuhei Deguchi, Toshiji Tada, Tsutomu Yasuda
Publikováno v:
Journal of Inorganic Biochemistry. 65:191-197
(Z)-2-(2-aminothiazol-4-yl)-N-(2-hydroxyethyl)-2-(hydroxyimino)acetamide (HL) has been employed as a model compound for an orally active cephalosporin antibiotic, Cefdinir (CFDN). A binuclear copper(II) complex Cu2L4 (1) has been obtained from an aqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1acf7248e536e31bad7ac271a82a6fb0
https://doi.org/10.1016/s0162-0134(96)00132-8
https://doi.org/10.1016/s0162-0134(96)00132-8
Degradation Kinetics and Isomerization of Cefdinir, a New Oral Cephalosporin, in Aqueous Solution. 1
Autor:
Yoshihiro Namiki, Junichi Matsushita, Mamoru Fujioka, Yoshihiko Okamoto, Kuniko Kiriyama, Tsutomu Yasuda
Publikováno v:
Journal of Pharmaceutical Sciences. 85:976-983
Hydrolytic degradation products of cefdinir were studied in acidic (pH 1), neutral (pH 6), and basic (pH 9) solutions. Seven major degradation products were isolated by preparative and/or high-performance liquid chromatography and characterized by UV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bedb6dd6b4f201478e7a2c62324d2a2a
https://doi.org/10.1021/js950446r
https://doi.org/10.1021/js950446r
Autor:
Yoshihiro Namiki, Tsutomu Yasuda, Junichi Matsushita, Mamoru Fujioka, Yoshihiko Okamoto, Kuniko Kiriyama
Publikováno v:
Journal of Pharmaceutical Sciences. 85:984-989
Hydrolysis of cefdinir leads to pH-dependent isomerizations and beta-lactam ring-opening. Lactam ring opened gamma-lactones were produced as a mixture of four diastereoisomers based on the lactone methyl, and C-6 isomerizations in acidic to neutral s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e2e2ca83de2cdca0f89887fc09f7d4
https://doi.org/10.1021/js950447j
https://doi.org/10.1021/js950447j
Autor:
Tsutomu Yasuda, Kohji Itoh, Yoshihiro Namiki, Junichi Matsushita, Yoshihiko Okamoto, Mamoru Fujioka
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 14:739-748
The validation of the HPLC method used for the determination of cefdinir and its related substances is described. The developed method was specific and stability-indicating and provided a linear response with concentration. The system and method prec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c294d129cda432a6a077b118df3c825c
https://doi.org/10.1016/0731-7085(95)01687-2
https://doi.org/10.1016/0731-7085(95)01687-2
Autor:
Tsutomu Yasuda, Shuhei Deguchi, Yoshihiko Okamoto, Marie T. Mooney, Mamoru Fujioka, Toshiji Tada
Publikováno v:
Chemical and Pharmaceutical Bulletin. 43:374-377
Cefdinir (CFDN) is an orally active, semisynthetic cephalosporin antibiotic and its structure is characterized by an oxyimino side chain which is able to form complexes with various metal ions. We observed that bioavailability of CFDN in dogs was red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0130c8b855b5a6417cbbdfdb8e58f50b
https://doi.org/10.1248/cpb.43.374
https://doi.org/10.1248/cpb.43.374
Autor:
Yuan-Ying Liu, Masakatsu Sudo, Mamoru Fujioka, Yoshiharu Kikawa, Akio Nakai, Yosuke Shigematsu
Publikováno v:
Pediatrics International. 36:112-115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0884c04d66a536d5c6a27383d67a8b4
https://doi.org/10.1111/j.1442-200x.1994.tb03143.x
https://doi.org/10.1111/j.1442-200x.1994.tb03143.x
Publikováno v:
Organic Mass Spectrometry. 25:80-82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da33747182bcb744d6118b76f97d1aa
https://doi.org/10.1002/oms.1210250117
https://doi.org/10.1002/oms.1210250117
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 203(2-3)
Isovaleric acidemia is an autosomal recessive inherited disorder due to a deficiency of isovaleryl-CoA dehydrogenase. Although two clinically different types of this disease, an acute neonatal form and a chronic intermittent form, have been reported,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c7540b8c19ee71236c6548fc3d7779d
https://pubmed.ncbi.nlm.nih.gov/1777996
https://pubmed.ncbi.nlm.nih.gov/1777996
Publikováno v:
Biomedicalenvironmental mass spectrometry. 19(13)
This investigation reports the low-energy collision-induced dissociation of the protonated molecules of polyamino alcohols, formed by chemical reduction of synthetic peptides and N-terminal blocked peptides, in order to evaluate its potential for pep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87a482187b134722aa3d18985b23aad
https://pubmed.ncbi.nlm.nih.gov/2099871
https://pubmed.ncbi.nlm.nih.gov/2099871