Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Naohiko Okada"'
Autor:
Toshiaki Kamimura, Kazuyo Miki, Naohiko Okada, Minoru Nishida, Yoshiko Yokota, Hiroshi Sakamoto, Shigemi Fukada, Shoji Nakamoto, Takeo Murakawa
Publikováno v:
The Journal of Antibiotics. 29:444-459
FR10612, like cephalexin, is a broad-spectrum oral cephalosporin derivative. The antimicrobial activity of FR10612 against clinical isolates was similar to cephalexin; however, at a low inoculum size its activity was greater than cephalexin against K
Autor:
Minoru Nishida, B.D. Rawal, K.R. Comber, Yohko Kohno, Tom Bergan, F. Fried, B.G. Charles, H. Held, Walter H. Traub, G.H. Valler, Hiroshi Sakamoto, Yoshiko Yokota, Ingrid Kleber, Takeo Murakawa, R. Sutherland, Naohiko Okada, M.J. Basker
Publikováno v:
Chemotherapy. 23:I-VI
Autor:
Hiroshi Sakamoto, Yoshiko Yokota, Shoji Nakamoto, Yoko Kono, Toshiaki Kamimura, Takeo Murakawa, Shigemi Fukada, Naohiko Okada, Minoru Nishida
Publikováno v:
Antimicrobial Agents and Chemotherapy. 11:51-63
FR10024 is a broad-spectrum antibiotic. The in vitro antibacterial activity of FR10024 against clinical isolates of Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae , and Proteus mirabilis is greater than that of any of the cephalospori
Autor:
Sachiko Goto, Naohiko Okada, Minoru Nishida, Toshiaki Kamimura, Yoshimi Matsumoto, Y Mine, Shogo Kuwahara
Publikováno v:
Antimicrobial Agents and Chemotherapy. 16:540-548
FK 749 is a new parenteral cephalosporin derivative which is more active against various gram-negative bacilli, including the opportunistic pathogens such as Enterobacter, Citrobacter species, and Serratia marcescens, than cephalosporins and cephamyc
Publikováno v:
Antimicrobial agents and chemotherapy. 14(1)
The bactericidal activity of cefazolin, cephaloridine, and cephalothin in a simulated intramuscular study (500 mg) and a simulated intravenous drip infusion study (2 g/2 h) is reported. In both model systems, the bactericidal activity of cefazolin su
Publikováno v:
Chemotherapy. 23(6)
Serum levels of FR10612 given orally to rats persisted significantly longer than did those of cephalexin. Since the elucidation of this phenomenon observed in rats is considered to be pertinent to the understanding of the drug kinetics of FR10612 in