Synthesis of Granuliberin-R and Various Fragment Peptides and Their Histamine-Releasing Activities
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概要
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Granuliberin-R and various fragment peptides were synthesized and their histaminereleasing activities were examined. The relative potencies of granuliberin-R, H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH_2,as liberators of histamine from mast cells are very similar to those of substance P and bradykinin. Studies on the histamine-releasing activity of various fragment peptides of granuliberin-R showed that a 4-amino acid central sequence, -Ile-Tyr-Arg-Arg-, is the minimum requirement for the releasing action of this frog skin peptide.
- 社団法人日本薬学会の論文
- 1980-03-25
著者
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牧 良孝
武田薬品中央研究所生物研
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矢島 治明
Faculty of Pharmaceutical Sciences, Kyoto University
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安原 義
東京農大
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藤野 政彦
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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藤野 政彦
武田薬品工業
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武山 正治
Department of Clinical Pharmacy, Oita Medical University
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中嶋 暉躬
Institute of Pharmaceutical Sciences, School of Medicine, Hiroshima University
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中嶋 暉躬
東京大学薬学部薬品分析化学教室
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平井 裕子
広島大学医学部総合薬学科
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藤野 政彦
武田薬品中央研
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藤野 政彦
Central Research Division, Takeda Chemical Industries Ltd.
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武山 正治
Department Of Clinical Pharmacy Oita Medical University
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藤野 政彦
武田薬品工業(株)
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北田 千恵子
Discovery Research Division Takeda Chemical Industries Ltd.
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Kitada Chieko
Discovery Research Division Takeda Chemical Industries Ltd
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矢島 治明
Faculty Of Pharmaceutical Sciences Kyoto University
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牧 良孝
武田薬品中央研
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芦田 康子
武田薬品工業株式会社研究開発本部・生物研究所
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芦田 康子
武田薬品工業
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