Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Yuhta Masuoka"'
Autor:
Yoichi Hayakawa, Kazuo Furihata, Haruo Seto, Kenichi Suzuki, Kazuo Shin-ya, Yuhta Masuoka, Koji Nagai
Publikováno v:
The Journal of Antibiotics. 54:187-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f72e5b79aff29c7a7062837597335c3
https://doi.org/10.7164/antibiotics.54.187
https://doi.org/10.7164/antibiotics.54.187
Autor:
Haruo Seto, Yuhta Masuoka, Kazuo Furihata, Kazuo Shin-ya, Koji Nagai, Atsuko Nagai, Kenichi Suzuki, Yoichi Hayakawa
Publikováno v:
Tetrahedron Letters. 42:41-44
Spiruchostatins A and B were isolated from Pseudomonas sp. as gene expression-enhancing substances. They possess novel bicyclic depsipeptides involving 4-amino-3-hydroxy-5-methylhexanoic acid and 4-amino-3-hydroxy-5-methylheptanoic acid residues, res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5909a2b26973cf15e80151eccd476570
https://doi.org/10.1016/s0040-4039(00)01874-8
https://doi.org/10.1016/s0040-4039(00)01874-8
Autor:
Kenichi Suzuki, Yong-Bae Kim, Haruo Seto, Minoru Yoshida, Yoichi Hayakawa, Kazuo Shin-ya, Yuhta Masuoka, Koji Nagai
Publikováno v:
The Journal of Antibiotics. 53:788-792
A new metabolite, diheteropeptin, was found in the culture broth of Diheterospora chlamydosporia Q58044 by screening for TGF-beta-like active substances. Diheteropeptin was extracted from the culture supernatant and purified by a series of chromatogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b5cc1ca0b7b525781940539610d9db
https://doi.org/10.7164/antibiotics.53.788
https://doi.org/10.7164/antibiotics.53.788
Autor:
Yuhta Masuoka, Koji Nagai, Kazuo Shin-ya, Kenichi Suzuki, Yukhhro Takebayashi, Kazuo Furihata, Yoichi Hayakawa, Hisao Matsumoto, Haruo Seto
Publikováno v:
The Journal of Antibiotics. 53:793-798
The structure of diheteropeptin (1), a TGF-beta-like active substance from Diheterospora chlamydosporia Q58044, was determined to be a new cyclotetrapeptide, cyclo[2aminoisobutyryl-(S)-phenylalanyl-(R)-prolyl-(2S,8R,9R)-2-am ino-8,9-dihydroxydecanoyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5976a3f8b3380d9ede40ad262a877800
https://doi.org/10.7164/antibiotics.53.793
https://doi.org/10.7164/antibiotics.53.793
Autor:
Haruo Seto, Kazuo Shin-ya, Yuhta Masuoka, Koji Nagai, Kazuo Furihata, Yoichi Hayakawa, Kenichi Suzuki
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c0673e75565a2260ed4ebff9563e7ef
https://doi.org/10.1002/chin.200131233
https://doi.org/10.1002/chin.200131233
Publikováno v:
Natural Compounds as Drugs ISBN: 9783764385941
Histone deacetylase (HDAC) inhibitors, such as trichostatin A and trapoxin, which were first found in microorganisms, potently and selectively inhibit HDAC enzymes. They have made a strong contribution to research on HDACs, chromatin control, abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03293862dbeaf6872d35b4a431334777
https://doi.org/10.1007/978-3-7643-8595-8_7
https://doi.org/10.1007/978-3-7643-8595-8_7
Publikováno v:
Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques. 66
Histone deacetylase (HDAC) inhibitors, such as trichostatin A and trapoxin, which were first found in microorganisms, potently and selectively inhibit HDAC enzymes. They have made a strong contribution to research on HDACs, chromatin control, abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ac6fb93d1de3372beb406ab7352ab8e9
https://pubmed.ncbi.nlm.nih.gov/18416310
https://pubmed.ncbi.nlm.nih.gov/18416310
Autor:
Aya Kita, Yuhta Masuoka, Nobuaki Amino, Kiyoshi Furuichi, Kin-Ya Sohda, Kazuo Oda, Masamichi Mori, Toshiyuki Sakai, Masatoshi Taniguchi, Masao Sasamata, Yoh Terada, Hitoshi Matsushime, Yoshihiro Sowa, Koji Nagai, Nobuaki Shindoh, Masaya Orita
Publikováno v:
International journal of oncology. 32(3)
Histone deacetylase (HDAC) inhibitors have been shown to have antitumor activity in vitro and in vivo. Various studies related to their antitumor activity and mechanism of action have been reported for HDAC inhibitors, but the relationship of their a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92f5feaa0d31baeb044875f8c162c08f
https://pubmed.ncbi.nlm.nih.gov/18292931
https://pubmed.ncbi.nlm.nih.gov/18292931
Publikováno v:
The Journal of Antibiotics. 50:1058-1060
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d125c2271fe5d7711a7631e57b4481c2
https://doi.org/10.7164/antibiotics.50.1058
https://doi.org/10.7164/antibiotics.50.1058
Autor:
Yuhta Masuoka, Yoichi Hayakawa, Kenichi Suzuki, Atsuko Nagai, Kazuo Furihata, Kazuo Shin-ya, Koji Nagai, Haruo Seto
Publikováno v:
ChemInform. 32
Spiruchostatins A and B were isolated from Pseudomonas sp. as gene expression-enhancing substances. They possess novel bicyclic depsipeptides involving 4-amino-3-hydroxy-5-methylhexanoic acid and 4-amino-3-hydroxy-5-methylheptanoic acid residues, res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22f95dcce920e228fea4cfcb0875d1d6
https://doi.org/10.1002/chin.200112193
https://doi.org/10.1002/chin.200112193