Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Masaro Shimizu"'
Autor:
Kiyoaki Katano, Kazue Sasaki, Takashi Tsuruoka, Masaro Shimizu, Shokichi Ohuchi, Yasuko Isomura, Mami Kawaguchi, Eiki Shitara, Tomoaki Miura
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2601-2606
The tetrahydrothienopyridine derivatives were derived from aminomethylcyclohexylcarboxylic acid as a lead moiety. Evaluation of the antiplatelet activity and receptor binding assay revealed that compound 1(ME3277) was a novel and potent non-peptide a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0789bb53e6a25e5a5cc30cedaadec4ac
https://doi.org/10.1016/0960-894x(96)00476-3
https://doi.org/10.1016/0960-894x(96)00476-3
Publikováno v:
ChemInform. 22
Twenty-five 8-amino-5, 6-quinolinediones were prepared by copper(II)-catalyzed oxidation of 6-quinolinol in methanol with secondary amines, or by oxidative demethylation of the corresponding 5, 6-dimethoxyquinolines in aqueous acetonitrile with ceriu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::110d387d0efb45a17cfc48a79d717ab5
https://doi.org/10.1002/chin.199119182
https://doi.org/10.1002/chin.199119182
Autor:
Masaro Shimizu, Eiki Shitara, Mami Kawaguchi, Yasuko Isomura, Takashi Tsuruoka, Shokichi Ohuchi, Kiyoaki Katano, Kazue Sasaki, Tomoaki Miura
Publikováno v:
ChemInform. 28
The tetrahydrothienopyridine derivatives were derived from aminomethylcyclohexylcarboxylic acid as a lead moiety. Evaluation of the antiplatelet activity and receptor binding assay revealed that compound 1(ME3277) was a novel and potent non-peptide a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3de191927527c1790def84203b11e6e0
https://doi.org/10.1002/chin.199714218
https://doi.org/10.1002/chin.199714218
Autor:
Manabu Akazawa, Yoshiyasu Kitahara, Akinori Kubo, Shinsuke Nakahara, Tatsuya Nakai, Masaro Shimizu
Publikováno v:
Chemical and Pharmaceutical Bulletin. 39:2256-2263
5, 8-Isopuinolinediones (12, 18, 25), 7, 8-isoquinolinediones (14, 19) and 5, 6-isoquinolinediones (26) were synthesized by oxidative demethylation of the corresponding dimethoxyisoquinolines with cerium(IV) ammonium nitrate or silver(II) oxide. 8-Di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::231203c7beea4f632473ef724f8f3a13
https://doi.org/10.1248/cpb.39.2256
https://doi.org/10.1248/cpb.39.2256
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:2841-2846
Twenty-five 8-amino-5, 6-quinolinediones were prepared by copper(II)-catalyzed oxidation of 6-quinolinol in methanol with secondary amines, or by oxidative demethylation of the corresponding 5, 6-dimethoxyquinolines in aqueous acetonitrile with ceriu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2da4025111dc800e768b31c8f9fbb4ae
https://doi.org/10.1248/cpb.38.2841
https://doi.org/10.1248/cpb.38.2841
Publikováno v:
HETEROCYCLES. 36:1909
2,5,8(1H)-Quinolinetriones (12), 2,5,6(1H)-quinolinetriones (13), 2-alkoxy-5,8-quinolinediones (14), 2,8-dimethoxy-5,6-quinolinedione (15), and 2,6-dimethoxy-7,8-quinolinediones (16) were synthesized by oxidative demethylation of the corresponding 2(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c949c5701e35b8a6387ad525240fdb6c
https://doi.org/10.3987/com-93-6404
https://doi.org/10.3987/com-93-6404
Autor:
Masaro Shimizu, Keiichiro Hozumi
Publikováno v:
BUNSEKI KAGAKU. 20:267-274
光学積分法による迅速酸素自動分析計では,有機酸素を高温の炭素層に通じ,一酸化炭素に変換し,これを五酸化ヨウ素と反応させて生成するヨウ素蒸気の吸光度を測定するが,光学的密度が
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4730e1a4199c309b0afe0088d701568d
https://doi.org/10.2116/bunsekikagaku.20.267
https://doi.org/10.2116/bunsekikagaku.20.267
Autor:
Keiichiro Hozumi, Masaro Shimizu
Publikováno v:
BUNSEKI KAGAKU. 19:1041-1049
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26e1694b3e85ced8e9e92f4ff90954a6
https://doi.org/10.2116/bunsekikagaku.19.1041
https://doi.org/10.2116/bunsekikagaku.19.1041