Studies on Peptides. XV. Synthesis of Prolyltyrosylarginylmethionine, the Tetrapeptide situated within the Amino Acid Sequences of Monkey and Human β-Melanocyte-stimulating Hormones.
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概要
- 論文の詳細を見る
Arginylmethionine was prepared by three different methods, one from N^α-benzyloxycarbonyl-N^G-tosylarginylmethionine with sodium in liquid ammonia and others, from N^α-benzyloxycarbonyl-N^G-nitroarginylmethionine by treatment with hydrogen fluoride, and from N^α-t-butoxycarbonyl-N^G-nitroarginylmethionine by treatment with stannous chloride in 80% formic acid. Arginylmethionine was coupled with N^α-t-butoxycarbonylprolyltyrosine via the azide method and the resulting peptide was treated with trifluoroacetic acid to give prolyltyrosylarginylmethionine, the tetrapeptide situated within the structures of monkey and human β-melanocyte-stimulating hormones.
- 社団法人日本薬学会の論文
- 1967-12-25
著者
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岡田 芳男
Faculty of Pharmaceutical Sciences Kobe-Gakuin University
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矢島 治明
Faculty of Pharmaceutical Sciences, Kyoto University
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木野村 保彦
Faculty of Pharmaceutical Sciences, Kyoto University
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大島 孝夫
Faculty of Pharmaceutical Sciences, Kyoto University
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大島 孝夫
Faculty Of Pharmaceutical Sciences Kyoto University
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矢島 治明
Faculty Of Pharmaceutical Sciences Kyoto University
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木野村 保彦
Faculty Of Pharmaceutical Sciences Kyoto University
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