Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yoko Misawa"'
Autor:
Yuanjun Gu, Yasuhiko Tabata, Yoshiyuki Kawakami, Appakaalai N. Balamurugan, Hiroshi Hori, Natsuki Nagata, Akira Satake, Wanxing Cui, Meirigeng Qi, Yoko Misawa, Maki Toma, Masaaki Miyamoto, Masumi Nozawa, Kazutomo Inoue M.D., Ph.D.
Publikováno v:
Cell Transplantation, Vol 10 (2001)
The subcutaneous space is a potential site for clinical islet transplantation. Even though there are several advantages, poor blood supply at this site mainly causes failure of islet survival. In this study, angiogenesis was induced in advance at the
Externí odkaz:
https://doaj.org/article/233d2353825b4e2bb95a0c28acbde642
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7da028918fa71aed46cda864faf22d29
https://doi.org/10.1002/chin.200206267
https://doi.org/10.1002/chin.200206267
Publikováno v:
The Journal of Antibiotics. 43:570-573
We describe the structure and antibacterial activity of the degradation products of 6-O-methylerythromycin A and its derivatives under acidic conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c6a21ee43870d58390c4dca26226e1
https://doi.org/10.7164/antibiotics.43.570
https://doi.org/10.7164/antibiotics.43.570
Autor:
Yoko Misawa, Tetsuya Tanikawa, Masakazu Sato, Toshifumi Asaka, Masato Kashimura, Shigeo Morimoto, Atsushi Nishida, Keiko Suzuki, Kazuya Kameo
Publikováno v:
Journal of medicinal chemistry. 44(24)
Introduction of an acyl group to the 3-O-position of erythromycin A derivatives instead of L-cladinose led to a novel class of macrolide antibiotics that we named "acylides". The 3-O-nitrophenylacetyl derivative TEA0777 showed significantly potent ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4213ac4b6c38fb1bdf92fb4850ebe293
https://pubmed.ncbi.nlm.nih.gov/11708904
https://pubmed.ncbi.nlm.nih.gov/11708904
Publikováno v:
The Journal of antibiotics. 54(8)
The novel 6-O-methyl tricyclic ketolides TE-802 and its analogs were synthesized by two successive cyclization reactions, 11,12-cyclic carbamate formation by intramolecular Michael addition and 9,11-diazaheptene ring construction by intramolecular de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f47beb465bea3e5ef8b5667d647ebab7
https://pubmed.ncbi.nlm.nih.gov/11592503
https://pubmed.ncbi.nlm.nih.gov/11592503
Autor:
Masato Kashimura, Yutaka Kawashima, Takeo Ono, Ikuo Moriguchi, Takatoshi Nagate, Yoko Misawa, Toshifumi Asaka, Yuki Yamada, Katsuo Hatayama, Sigeo Morimoto, Shuichi Hirono
Publikováno v:
Chemicalpharmaceutical bulletin. 42(5)
In order to develop new-generation macrolide antibiotics active against erythromycin (EM)-resistant strains, a series of 6-O-methyl EM 9-O-substituted oxime derivatives was synthesized and evaluated for antibacterial activity against EM-resistant (S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb3feb80f3b42c8f0053a0da026ab599
https://pubmed.ncbi.nlm.nih.gov/8069961
https://pubmed.ncbi.nlm.nih.gov/8069961
Autor:
Takatoshi Nagate, Yoko Misawa, Yoshiaki Watanabe, Sadafumi Omura, Takashi Adachi, Shigeo Morimoto
Publikováno v:
The Journal of antibiotics. 43(5)
6-O-Methylerythromycin B has been synthesized from erythromycin B via regioselective methylation of the 6-hydroxyl group in 71 % overall yield. This compound shows in vitro antibacterial activity comparable to erythromycins A and B and exhibits super
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b34493a9ab5b5ff2d1830016643c8c
https://pubmed.ncbi.nlm.nih.gov/2358406
https://pubmed.ncbi.nlm.nih.gov/2358406
Autor:
Kazuo Numata, Yoko Misawa, Kazuhiko Sugita, Sadafumi Omura, Junko Miyachi, Kenji Yamada, Takeo Ono, Takatoshi Nagate, Shigeo Morimoto
Publikováno v:
The Journal of antibiotics. 43(3)
The in vitro and in vivo antibacterial activities of 6-O-methylerythromycin A (TE-031, A-56268, or clarithromycin) and 6, 11-di-O-methylerythromycin A (TE-032) have been compared with those of erythromycin A (EM) and josamycin (JM). TE-031 and TE-032
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dae3b717c83ba00cb27ccd4c6130d53
https://pubmed.ncbi.nlm.nih.gov/2139023
https://pubmed.ncbi.nlm.nih.gov/2139023
Autor:
Wanxing Cui, Yoshiyuki Kawakami, Masumi Nozawa, Yoko Misawa, Akira Satake, Yuanjun Gu, Meirigeng Qi, Hiroshi Hori, Kazutomo Inoue, Yasuhiko Tabata, A. N. Balamurugan, Natsuki Nagata, Masaaki Miyamoto, Maki Toma
Publikováno v:
ResearcherID
Cell Transplantation, Vol 10 (2001)
Cell Transplantation, Vol 10 (2001)
The subcutaneous space is a potential site for clinical islet transplantation. Even though there are several advantages, poor blood supply at this site mainly causes failure of islet survival. In this study, angiogenesis was induced in advance at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cf92c7d45f6849c9f713076a4b1535b
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000170544500019&KeyUID=WOS:000170544500019
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000170544500019&KeyUID=WOS:000170544500019
