发明名称 COMPOUND HAVING INHIBITORY ACTIVITY OF FAS-INDUCED APOPTOSIS AND ITS PREPARATION
摘要 PROBLEM TO BE SOLVED: To prepare the subject new compound capable of inhibiting apoptosis induced by Fas stimulation, and useful as a therapeutic agent of a neurodegenerative disease such as Alzheimer's disease and Parkinson's disease, amyotrophic lateral sclerosis, acquired immunodeficiency syndrome or the like. SOLUTION: This new compound is the compound of formula I [R<1> and R<2> are each hydroxy, silyloxy, H, an alkyl or the like; R<3> and R<4> are each H, a (substituted) alkyl, formyl or the like; R<5> and R<6> are each H, a (substituted) alkyl, a (substituted) alkenyl or the like; R<7> and R<8> are each hydroxy, H, an alkyl or the like; R<9> and R<10> are each H, a halogen or the like], e.g. a compound of formula II. The compound of formula I is obtained by culturing microorganisms belonging to the genus Paecilomyces preferably at 20-25 deg.C at pH6-8 for several days to several weeks, and separating and purifying the produced compound from the culturing material. The medium is the one containing a carbon source (e.g. glucose), a nitrogen source (e.g. soybean powder) and an inorganic salt (e.g. calcium carbonate).
申请公布号 JPH11222456(A) 申请公布日期 1999.08.17
申请号 JP19980294043 申请日期 1998.10.15
申请人 SHIONOGI & CO LTD 发明人 KANBAYASHI YOSHIKAZU;KAMIGAICHI TOSHIYUKI;HORIBE ISAO
分类号 C12P7/26;A61K31/00;A61K31/075;A61K31/11;A61K31/12;A61K31/21;A61K31/29;A61K31/335;A61K31/336;A61K31/34;A61K31/343;A61K31/35;A61K31/352;A61K31/695;A61P9/00;A61P25/00;A61P25/28;A61P37/00;A61P37/02;A61P43/00;C07C49/743;C07D303/14;C07D307/77;C07D311/74;C07D311/76;C07F7/18;C12P7/40;C12P17/02;C12P17/18;C12R1/79;(IPC1-7):C07C49/743 主分类号 C12P7/26
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