Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Tsutomu Katakami"'
Autor:
Tsutomu Katakami, Joji Kamiya, Nobuya Kawauchi, Tadahito Nobori, Tatsuo Kaiho, Haruki Mori, Michihiko Miyamoto, Kunio Sannohe, Tatsuro Yokoyama
Publikováno v:
Journal of Medicinal Chemistry. 35:3325-3330
A series of 6-[(2-aminoethyl)amino]-1,3-dimethyl-2,4(1H,3H)- pyrimidinedione derivatives were synthesized and studied for their class III electrophysiological activity and class II (beta-blocking) effects in in vitro and in vivo models. Structure-act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::494840e2071ca6c937ab00f7b055fc46
https://doi.org/10.1021/jm00096a003
https://doi.org/10.1021/jm00096a003
Publikováno v:
Japanese Journal of Pharmacology. 58:107-115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84cd50b6f2a2cc1444733f5026f55a8e
https://doi.org/10.1016/s0021-5198(19)39753-7
https://doi.org/10.1016/s0021-5198(19)39753-7
Publikováno v:
ChemInform. 35
During the past decade, much attention has been directed toward the development of potassium channel blockers, which were expected to be a novel type of antiarrhythmic agent. Pharmacological screening for new cardiovascular agents led us to discover
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2716069fd638978de704697f72ceb184
https://doi.org/10.1002/chin.200424243
https://doi.org/10.1002/chin.200424243
Publikováno v:
Journal of Molecular and Cellular Cardiology. 22:S70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a31e9c6357adb0ab2ffd8a9f44694c99
https://doi.org/10.1016/0022-2828(90)91735-p
https://doi.org/10.1016/0022-2828(90)91735-p
Autor:
Tsutomu Katakami, Tatsuro Yokoyama, Masaaki Ishii, Makoto Hirayama, Hitoshi Banno, Joji Kamiya
Publikováno v:
Japanese Journal of Pharmacology. 52:250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ef01d9bb1420b81fb56a147d7465fda
https://doi.org/10.1016/s0021-5198(19)55574-3
https://doi.org/10.1016/s0021-5198(19)55574-3
Autor:
Tsutomu Katakami, Joji Kamiya, Kanji Yoshihara, Akihiro Oyabe, Mie Nakamura, Michihiko Miyamoto, Masaaki Ishii
Publikováno v:
Japanese Journal of Pharmacology. 52:251
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e5026ff86f83d29f4bc1c82de5cc2b7
https://doi.org/10.1016/s0021-5198(19)55575-5
https://doi.org/10.1016/s0021-5198(19)55575-5
Publikováno v:
Bulletin of the Chemical Society of Japan. 49:297-301
Syntheses of dimethyldiphenyl-(VI and XII) and tetraphenyltetrakisdehydro[18]annulenes (XVII) have been performed. It was found that the reaction sequence used for the synthesis of tetramethyltetrakisdehydro[18]annulene can be used generally for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adcf8b9f04a0da988d1af57862795b5a
https://doi.org/10.1246/bcsj.49.297
https://doi.org/10.1246/bcsj.49.297
Publikováno v:
Tetrahedron Letters. 9:1115-1120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dec8ef0dc50e0d13918503f5d3aa2c31
https://doi.org/10.1016/s0040-4039(01)98903-8
https://doi.org/10.1016/s0040-4039(01)98903-8
Autor:
Takayoshi Kashitani, Masazumi Nakagawa, Masahiko Iyoda, Ryonosuke Muneyuki, Tsutomu Katakami, Mamoru Morimoto, Motomu Tanaka
Publikováno v:
Bulletin of the Chemical Society of Japan. 46:2565-2570
Substituted 2,8-decadien-4,6-diyndials (I, II and III) were synthesized by the oxidative coupling of corresponding substituted pentenynals (VII and XIII) or acetal (XI). It was found that decadiendiyndials (I, II and III) give readily dihydrofuranyli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f121c247921259571131fd7e6d25315
https://doi.org/10.1246/bcsj.46.2565
https://doi.org/10.1246/bcsj.46.2565
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbc8626c12f06e7de88efaa9f5a79578
https://doi.org/10.1002/chin.197617169
https://doi.org/10.1002/chin.197617169