发明名称 NEUROTROPIC PEPTIDE DERIVATIVE
摘要 <p>NEW MATERIAL:A neurotropic peptide derivative expressed by the formula (A<6> is A<5>-Gln, etc.; A<5> is A<4>-Ser, etc.; A<4> is A<3>-Ile, etc.; A<3> is A<2>-Asp, etc.; A<2> is A<1>-Ala, etc.; A<1> is X-D-Ala. X-Tyr, etc.; X is H, acyl, etc.; A<7> is Trp-A<8>, etc.; A<8> is Y, Ala-A<9>, etc.; A<9> is Y, Gly-A<10>, etc.; A<10> is Y, Pro-A<11>, etc.; A<11> is Y or Leu-Y; Y is OH, amide residue or ester residue). USE:A medicine for nervous degenerative diseases such as Alzheimer disease, Parkinson disease or amyotrophic lateral sclerosis. PREPARATION:For example, a C-terminal amino acid having protected amino group is bound to an insoluble support with the carboxyl group thereof by a solid-phase method and the amino-protecting group is removed. Amino acids having protected amino groups are then bound according to the amino acid sequence of the objective peptide to synthesize the whole sequence. The resultant peptide is subsequently removed from the support to remove the protecting groups. Bondages, as necessary, are further formed between side chains to afford the objective peptide derivative.</p>
申请公布号 JPH04124198(A) 申请公布日期 1992.04.24
申请号 JP19900243003 申请日期 1990.09.12
申请人 SUMITOMO PHARMACEUT CO LTD;KOJIKA YUKIO;YAMAMOTO MASAHIKO 发明人 UEKI YASUYUKI;FUKUSHIMA NOBUYUKI;IKEDA ZENJI;NISHIHARA NORIO;ONO KEIICHI;IRIE TSUNEMASA
分类号 A61K38/00;A61P25/00;A61P25/28;C07K5/06;C07K7/06;C07K7/56 主分类号 A61K38/00
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