发明名称 PROCESS FOR PREPARING CYCLIC PEPTIDE NUCLEUS
摘要 <p><CHEM> wherein R<1> is H or OH and; when R<1> is H, R<2> is H and R<3> and R<4> are both H or both OH, and when R<1> is OH, R<2> is H, R<3> is OH or C1-C6 alkyloxy and R<4> is OH, or R<2> is -@-NH2 and R<3> and R<4> are both OH, and the acid addition salts thereof. Cyclic peptide nuclei for formula 1 are prepared by the enzymatic deacylation of an appropriate antibiotic using an enzyme produced by the Actinoplanaceae, preferably by Actinoplanes utahensis. NRRL 12052. The cyclic peptide nuclei and the salts thereof are useful intermediates in the preparation of new semi-synthetic antifungal agents.</p>
申请公布号 PT72153(A) 申请公布日期 1981.01.01
申请号 PT19800072153 申请日期 1980.12.04
申请人 ELI LILLY AND COMPANY 发明人 BERNARD JOHN ABBOTT;DAVID SHUICHI FUKUDA
分类号 C12P21/04;A61K38/00;A61P31/04;C07K7/56;C07K7/60;C07K14/195;C07K14/41;C12P21/02;C12R1/045;(IPC1-7):07D/ 主分类号 C12P21/04
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