Syntheses and biological activities of neurokinin B analogs modified at positions 2, 3, and 6.
スポンサーリンク
概要
- 論文の詳細を見る
Nine neurokinin B [NKB] related octa- and nona-peptides containing Arg and <I>N</I>-methylglycine, D-Ala, D-Phe, D-Trp, D-α-aminophenylacetic acid, D-Arg, D-Pro, D-homoglutamine, or D-homoglutamic acid instead of Met<SUP>2</SUP> or His<SUP>3</SUP>, and Phe<SUP>6</SUP>, respectively, in the original sequences were synthesized by standard solid phase method. The biological activities of the analogs were assayed on isolated guinea-pig ileum. [Arg<SUP>3</SUP>, D-Ala<SUP>6</SUP>]–NKB (3–10) was found to act as an antagonist of NKB.
- 公益社団法人 日本化学会の論文
著者
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Kurosawa Katsuro
School Of Pharmacy Hokuriku University
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HASHIMOTO TADASHI
School of Pharmacy, Hokuriku University
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Uchida Yoshiki
School Of Pharmacy Hokuriku University
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Sakura Naoki
School of Pharmacy, Hokuriku University
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Hirose Kyoko
School of Pharmacy, Hokuriku University
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Okimura Keiko
School of Pharmacy, Hokuriku University
関連論文
- Synthesis of Neurokinin B Analogs and Their Activities as Agonists and Antagonists(Organic,Chemical)
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- Syntheses and biological activities of neurokinin B analogs modified at positions 2, 3, and 6.
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