发明名称 PEPTIDE
摘要 <p>NEW MATERIAL:A peptide wherein the same or different T cell-recognizing sites of an acetyl choline acceptor alpha-subunit are conjugated to both the terminals of a B cell-recognizing site. USE:A drug treating and diagnosing myasthenia gravis. PREPARATION:The peptide wherein the same or different T cell-recognizing sites of an acetyl choline acceptor alpha subunit are conjugated to both the terminals of a B cell-recognizing site is synthesized e.g. by a solid phase synthetic method. An amino acid sequence whose alpha-amino groups, etc., are protected is bound in order to a solid carrier from the C-terminal side of the peptide in accordance to the amino acid sequence of the peptide in the presence of a condensing agent, and the alpha-amino-protecting group, is removed. The processes are repeated to synthesize a protected peptide chain on the solid carrier, and the product is subjected to a protecting group-removing reaction and to the separation of the peptide from the solid carrier by the use of an HF reaction device, followed by purifying the peptide by a high performance liquid chromatography to provide the novel peptide.</p>
申请公布号 JPH04193897(A) 申请公布日期 1992.07.13
申请号 JP19900327381 申请日期 1990.11.27
申请人 KURARAY CO LTD;TAKAMORI MASAHARU 发明人 TAKAMORI MASAHARU;OKUMURA SEIICHI;TANIHARA MASAO;OKA KIICHIROU
分类号 A61K38/00;A61K49/00;A61P43/00;C07K7/08;C07K14/705;C07K19/00 主分类号 A61K38/00
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