Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Masatomo Fukasawa"'
Autor:
Yoshihiro Sumita, Masatomo Fukasawa
Publikováno v:
Chemotherapy. 42:47-56
Two genetically distinct classes of meropenem-low-susceptibility Pseudomonas oaeruginosa PA02152 mutants, which arose spontaneously, were isolated. Two meropenem resistance genes, &
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae688f315a2e752da016db6267994b3e
https://doi.org/10.1159/000239421
https://doi.org/10.1159/000239421
Publikováno v:
Journal of Antimicrobial Chemotherapy. 35:473-481
We devised an accurate procedure with which to measure the affinities of beta-lactam antibiotics for penicillin-binding protein (PBP) 2' in methicillin-resistant Staphylococcus aureus (MRSA). In the present study, we used two isogenic strains of MRSA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ca037fe37dbe707903c34bf0fb7eb74
https://doi.org/10.1093/jac/35.4.473
https://doi.org/10.1093/jac/35.4.473
Publikováno v:
Chemotherapy. 41:172-177
We detected a novel protein with [14C]benzylpenicillin (PCG)-binding capacity and a molecular mass of about 60 kD in methicillin-resistant Staphylococcus aureus using a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dae4d5d339662b4ebec1e7d4a8e8527
https://doi.org/10.1159/000239340
https://doi.org/10.1159/000239340
Autor:
Yoshihiro Sumita, Akira Sasaki, Hisatoshi Shinagawa, Hiroshi Yamaga, Makoto Sunagawa, Masatomo Fukasawa
Publikováno v:
The Journal of Antibiotics. 47:1354-1358
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86f643032429bb6d43cfb10ed1b92964
https://doi.org/10.7164/antibiotics.47.1354
https://doi.org/10.7164/antibiotics.47.1354
Autor:
Kiyoshi Taya, Kazuo Kumagai, Masatomo Fukasawa, Akio Fukui, Masaru Fukui, Shigeyasu Nabeshima
Publikováno v:
The Journal of Antibiotics. 46:972-978
An actinomycete strain SC-4710, a new soil isolate, was found to produce a new macrolide antibiotic, PC-766B. Chemotaxonomic analysis of the producing organism revealed that the cells of SC-4710 had type IV cell wall, type A whole cell sugar pattern,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66083629e9c2531bc29db6777b2f9213
https://doi.org/10.7164/antibiotics.46.972
https://doi.org/10.7164/antibiotics.46.972
Publikováno v:
The Journal of Antibiotics. 45:500-504
A series of new penem compounds with a C-2 side chain consisting of a pyrrolidin-3'-ylthio group substituted with various aminocarbonyl groups at the C-5' position have been prepared. Antibacterial activity, stability to renal dehydropeptidase-I and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7c6c11523a5246c8baba21e0790cb96
https://doi.org/10.7164/antibiotics.45.500
https://doi.org/10.7164/antibiotics.45.500
Publikováno v:
The Journal of Antibiotics. 45:971-976
A series of 1 beta-methylcarbapenem compounds, which have a 5'-substituted-N-methylpyrrolidin-3'-ylthio group as a C-2 side chain, have been prepared and their biological properties were investigated. Substitution with a methyl group on the nitrogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aa6b288a717ee13588cf98266259dda
https://doi.org/10.7164/antibiotics.45.971
https://doi.org/10.7164/antibiotics.45.971
Publikováno v:
The Journal of Antibiotics. 43:314-320
We investigated the binding affinities of SM-7338 for penicillin-binding proteins (PBPs) and the morphological changes induced by it compared with those of imipenem. Both SM-7338 and imipenem had the highest binding affinities for PBP-2 of Escherichi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6cca41bdfededc78789b7421f64c109
https://doi.org/10.7164/antibiotics.43.314
https://doi.org/10.7164/antibiotics.43.314
Publikováno v:
The Journal of Antibiotics. 43:519-532
A series of new carbapenem compounds, which have a pyrrolidin-3'-ylthio group substituted with various aminocarbonyl group at C-5' position as C-2 side chain, have been prepared. The antibacterial activity and the stability to renal dehydropeptidase-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d08433c7483e5aeb1593491e7b0e1aa4
https://doi.org/10.7164/antibiotics.43.519
https://doi.org/10.7164/antibiotics.43.519
Autor:
Masatomo Fukasawa
Publikováno v:
Nihon Ishinkin Gakkai zasshi = Japanese journal of medical mycology. 46(4)
Liposomal amphotericin B (AmBisome) is a DDS (drug delivery system) formulation of amphotericin B (AMPH-B), and has been developed in an attempt to reduce the toxicity of AMPH-B while retaining its therapeutic efficacy. AMPH-B has been the "gold stan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee9fe00688118283d4a6c087d24670d
https://pubmed.ncbi.nlm.nih.gov/16282964
https://pubmed.ncbi.nlm.nih.gov/16282964