Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kantaro Ushiroda"'
Publikováno v:
Journal of Materials Chemistry. 10:2507-2514
The direct redox reaction between tetracyanoethylene (TCNE) and a planar porphyrinatomanganese(II), octakis(2,3,7,8,12,13,17,18-methylthio)porphyrinatomanganese(II), MnIIOMTP, produced a polymeric electron transfer salt (ETS), that has been structura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e518d0b5b82f18dec536a7c1b92ea71
https://doi.org/10.1039/b006261h
https://doi.org/10.1039/b006261h
Autor:
Atsushi Tsuchida, Kiyotaka Iwai, Katsunori Maruta, Jun Nagamine, Kantaro Ushiroda, Ryu Nagata, Mutsuo Taiji, Makoto Kitoh
Publikováno v:
ChemInform. 42
A series of benzoylpyrrole-based carboxylic acids are designed and synthesized as peroxisome proliferator-activated receptor (PPAR) activators.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83ceef099c80d7e17b77bcd8a7b6712e
https://doi.org/10.1002/chin.201119208
https://doi.org/10.1002/chin.201119208
Autor:
Yasuhiro Sato, Shinji Horai, Mutsuo Taiji, Katsunori Maruta, Kantaro Ushiroda, Kazunori Yanagi, Takeshi Takazawa, Tetsuya Kohno, Ryu Nagata, Tomokazu Nagano
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(7)
In our search for new PPARα/γ agonists, we designed and synthesized a series of benzoylazole-based carboxylic acids. Compound 9 showed potent PPARγ partial agonistic activity with modest PPARα agonistic activity. The sodium salt of 9 (9Na) demons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2932ab8a342ec79c0ecdbba09cfb2474
https://pubmed.ncbi.nlm.nih.gov/21377875
https://pubmed.ncbi.nlm.nih.gov/21377875
Autor:
Mutsuo Taiji, Ryu Nagata, Jun Nagamine, Makoto Kitoh, Katsunori Maruta, Kantaro Ushiroda, Kiyotaka Iwai, Atsushi Tsuchida
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(1)
Starting with a subtle blood glucose-lowering effect of a TGF-β inhibitor, we designed and synthesized a series of benzoylpyrrole-based carboxylic acids as PPARs activators. Among these compounds, 10sNa exhibited favorable blood glucose-lowering eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa161602d0e0dffd14cc5b92db25c55
https://pubmed.ncbi.nlm.nih.gov/21130649
https://pubmed.ncbi.nlm.nih.gov/21130649
Publikováno v:
ChemInform. 29
Tetraphenylporphyrins substituted with methylchalcogeno groups (XMe: X = Te, Se, S, and O) were prepared. Crystal structure analysis revealed that a novel type of molecular alignments was achieved by intermolecular CH···π interactions between XCH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c421b901ad5d5d8d1277066987cb9ba
https://doi.org/10.1002/chin.199806146
https://doi.org/10.1002/chin.199806146
Autor:
Takuya Matsumoto, Yoshio Takai, Tomoji Kawai, Satoshi Ohkouchi, Kantaro Ushiroda, Yoshiteru Sakata, Yasuhisa Naitoh, Ken-ichi Sugiura
Publikováno v:
ChemInform. 31
A novel porphyrin-fused porphyrin is formed by an oligomerization reaction of a (porphyrinato)nickel complex with TeCl4; the isolated compound, [2]porphyracene, was characterized by spectroscopic methods and direct observation using scanning tunnelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ded3482cbfb0e206ffea7e1f6bbc129
https://doi.org/10.1002/chin.200002140
https://doi.org/10.1002/chin.200002140
Autor:
Yasuhisa Naitoh, Ken-ichi Sugiura, Yoshio Takai, Takuya Matsumoto, Satoshi Ohkouchi, Tomoji Kawai, Yoshiteru Sakata, Kantaro Ushiroda
Publikováno v:
Chemical Communications. :1957-1958
A novel porphyrin-fused porphyrin is formed by an oligomerization reaction of a (porphyrinato)nickel complex with TeCl4; the isolated compound, [2]porphyracene, was characterized by spectroscopic methods and direct observation using scanning tunnelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0bfa5853eb1acfa7faf12400cdb16d0
https://doi.org/10.1039/a906073a
https://doi.org/10.1039/a906073a
Publikováno v:
Chemistry Letters. 26:927-928
Tetraphenylporphyrins substituted with methylchalcogeno groups (XMe: X = Te, Se, S, and O) were prepared. Crystal structure analysis revealed that a novel type of molecular alignments was achieved by intermolecular CH···π interactions between XCH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b094f732d96a7bacf765d94772d4506a
https://doi.org/10.1246/cl.1997.927
https://doi.org/10.1246/cl.1997.927