Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mayumi Shimamura"'
Autor:
Mitsushi KOBAYASHI, Kouji FURUUCHI, Jin ONODERA, Fumiaki KOIKE, Yoshihiro TSUJI, Mayumi SHIMAMURA, Hajime TOYOFUKU
Publikováno v:
Journal of the Japan Veterinary Medical Association. 76:e105-e109
Autor:
Ryuichi Kiyama, Yasuhiko Kanda, Susumu Kamata, Yasunobu Ishihara, Takeshi Shiota, Michio Ishikawa, Mayumi Shimamura, Toshiro Konoike, Koji Yoshimura, Nobuhiro Haga, Sanji Hagishita, Yasushi Murakami, Koji Abe, Kaoru Seno
Publikováno v:
Bioorganic & Medicinal Chemistry. 5:1695-1714
A novel series of CCK-B/gastrin receptor antagonists—ureidomethylcarbamoylphenylketone derivatives—were designed, synthesized, and evaluated for activity. Structure-activity relationship studies revealed the importance of a carboxylic acid at sub
Autor:
Yasuyuki Kawanishi, Shoichi Ishihara, Tadahiko Tsushima, Mayumi Shimamura, Kaoru Seno, Noriko Shima, Masanori Miyagoshi, Yasunobu Ishihara, Sanji Hagishita, Michio Ishikawa
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:1427-1430
The chemical modification of the dual histamine H2 and gastrin receptor antagonists described in our preceding paper, particularly the modification of spacers as well as the alteration of their connecting bonds at the gastrin receptor antagonist site
Autor:
Yasuyuki Kawanishi, Sanji Hagishita, Masanori Miyagoshi, Mayumi Shimamura, Tadahiko Tsushima, Shoichi Ishihara, Michio Ishikawa, Noriko Shima, Yasunobu Ishihara, Kaoru Seno
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:1421-1426
The joint type of hybrid molecules composed of two pharmacophore moieties taken from histamine H2 and gastrin receptor antagonists have been designed and synthesized to exhibit dual histamine H2 and gastrin receptor antagonistic activities. Here we r
Autor:
Makoto Kii, Michiko Ishikawa, Shin-ichi Mihara, Hirokazu Hara, Kohji Hanasaki, Sanji Hagishita, Tetsuo Okada, Yasushi Murakami, Mayumi Shimamura, Goro Kato, Masafumi Fujimoto, Hiroshi Hashizume, Yasunobu Ishihara
Publikováno v:
Journal of medicinal chemistry. 42(14)
A novel series of potent and selective non-peptide neuropeptide Y (NPY) Y1 receptor antagonists, having benzazepine nuclei, have been designed, synthesized, and evaluated for activity. Chemical modification of the R(1) and R(3) substituents in struct
Autor:
Yasunobu Ishihara, Susumu Kamata, Sanji Hagishita, Mayumi Shimamura, Kaoru Seno, Michio Ishikawa, Nobuhiro Haga
Publikováno v:
Bioorganicmedicinal chemistry. 5(7)
A series of CCK-B/gastrin receptor antagonists, 2,4-dioxo-1,5-benzodiazepine derivatives with a plane of symmetry, were designed, synthesized, and evaluated for antagonistic activity. Structure-activity relationship studies revealed that carbonylmeth
Autor:
Yasushi, MURAKAMI, Hirokazu, HARA, Tetsuo, OKADA, Hiroshi, HASHIZUME, Makoto, KII, Yasunobu, ISHIHARA, Michiko, ISHIKAWA, Mayumi, SHIMAMURA, Shin-ichi, MIHARA, Goro, KATO, Kohji, HANASAKI, Sanji, HAGISHITA, Masafumi, FUJIMOTO
Publikováno v:
岐阜藥科大學紀要 = The annual proceedings of Gifu College of Pharmacy. 49:80
Publikováno v:
Japanese Journal of Pharmacology. 79:199