Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hiroomi, Watabe"'
Autor:
Hiroomi Watabe
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 55:229-234
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad7c77110b60beeb132f5c362425880a
https://doi.org/10.5059/yukigoseikyokaishi.55.229
https://doi.org/10.5059/yukigoseikyokaishi.55.229
Autor:
Maki Watanabe, Hideyo Yamaguchi, Hiroomi Watabe, Tomio Takeuchi, Hiromi Tohyama, Shinichi Kondo, Tamio Hiratani, Shigeharu Inoue
Publikováno v:
The Journal of Antibiotics. 50:1042-1051
The mechanism of fungitoxic action of an antifungal antibiotic benanomicin A was studied with intact cells and protoplasts of Saccharomyces cerevisiae as well as with its enzymic preparations. The results obtained are summarized as follows: (1) benan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d11ef114918590e7a5c398a1dab20f0e
https://doi.org/10.7164/antibiotics.50.1042
https://doi.org/10.7164/antibiotics.50.1042
Autor:
Hiroomi Watabe, Shigeharu Inouye, Toru Sasaki, Masahiro Hatsu, Mieko Nagasawa, Masaji Sezaki, Shinichi Kondo, Shinji Miyadoh, Takashi Shomura
Publikováno v:
The Journal of Antibiotics. 45:320-324
A new antitumor antibiotic SF2575 has been isolated from a culture filtrate of Streptomyces sp. SF2575. The molecular formula was determined to be C40H43NO15 by elemental analysis, mass and 13C NMR spectral analyses. The spectral data revealed SF2575
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eb95be3ab6d76e9b4ad814785b973e4
https://doi.org/10.7164/antibiotics.45.320
https://doi.org/10.7164/antibiotics.45.320
Publikováno v:
The Japanese journal of antibiotics. 56(6)
We examined the effects of fosfomycin (FOM), norfloxacin (NFLX), kanamycin (KM), chloramphenicol (CP), and ampicillin (ABPC) on the morphology of E. coli O157:H7, and the accumulation (cell fraction) and release (medium fraction) of Shiga toxins (Stx
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f8b7f9b56d252a2d2368e4a0889c95e
https://pubmed.ncbi.nlm.nih.gov/15007877
https://pubmed.ncbi.nlm.nih.gov/15007877
Autor:
Kazumasa Aizawa, Atsuyuki Shimizu, Shiro Sakakibara, Hiroomi Watabe, Toshihiko Takata, Kyoichi Totsuka
Publikováno v:
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy. 10(2)
Pharmacokinetic and pharmacodynamic (PK/PD) parameters, which are important indices of the therapeutic efficacy of antimicrobials, and the minimum inhibitory concentration (MIC) predictive of clinical efficacy at common clinical doses, were examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c605bc103713d514ecf5badb8703753
https://pubmed.ncbi.nlm.nih.gov/15160313
https://pubmed.ncbi.nlm.nih.gov/15160313
Publikováno v:
The Japanese journal of antibiotics. 56(2)
Antibacterial activity of biapenem (BIPM) against clinical isolates of 8 species between 2000 and 2002 was compared with those of imipenem/cilastatin (IPM/CS), meropenem (MEPM), panipenem/betamipron (PAPM/BP) and ceftazidime (CAZ). The MICs of biapen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3f0ed4e4bf1639de676420a1b6b3650d
https://pubmed.ncbi.nlm.nih.gov/12825414
https://pubmed.ncbi.nlm.nih.gov/12825414
Publikováno v:
ChemInform. 34
PF1163A and B are a pair of antifungal agents isolated from a fermentation broth of Penicillium sp. PF1163A inhibited ergosterol synthesis in Saccharomyces cerevisiae, resulting in an accumulation of 4,4-dimethylzymosterol and a decrease of ergostero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a088360f209defdec620328e9c88ea6
https://doi.org/10.1002/chin.200317216
https://doi.org/10.1002/chin.200317216
Publikováno v:
The Japanese journal of antibiotics. 55(6)
In vitro antibacterial activity of fosfomycin was evaluated by various methods. Strains of methicillin-sensitive Staphylococcus aureus, methicillin-sensitive coagulase-negative Staphylococci and Escherichia coli were much more susceptible when glucos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f25577d844d77a833b63511c7055221
https://pubmed.ncbi.nlm.nih.gov/12621737
https://pubmed.ncbi.nlm.nih.gov/12621737
Autor:
Masaki, Shimizu, Makiko, Tabata, Tetsuro, Hara, Minako, Araake, Hiroomi, Watabe, Takeshi, Nishino
Publikováno v:
The Japanese journal of antibiotics. 55(6)
The in vitro short-term bactericidal activity and accumulation of NM394, the active metabolite of prulifloxacin, was compared with those of ciprofloxacin (CPFX), levofloxacin (LVFX) and gatifloxacin (GFLX), using Staphylococcus aureus, Escherichia co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98c360c30346e22abbc062b38a603db4
https://pubmed.ncbi.nlm.nih.gov/12621733
https://pubmed.ncbi.nlm.nih.gov/12621733
Publikováno v:
The Japanese journal of antibiotics. 55(6)
The inhibitory activity of NM394, the active form of the prodrug prulifloxacin, against type II topoisomerase from Pseudomonas aeruginosa was compared with those of ciprofloxacin (CPFX), levofloxacin (LVFX) and gatifloxacin (GFLX). The 50% inhibitory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24d267ec41fcfc88b571875eb1d2ffdf
https://pubmed.ncbi.nlm.nih.gov/12621742
https://pubmed.ncbi.nlm.nih.gov/12621742