摘要
利用自建的乙酰胆碱酯酶抑制剂的高通量筛选模型,从大量真菌中筛选到1株阳性菌株F01-2076.该菌株的发酵液经有机溶剂提取、硅胶柱层析及HPLC ODS反相柱层析分离,得到1个活性化合物F01-2076A,该化合物对乙酰胆碱酯酶的IC50为23.4μmol/L.通过对该化合物的紫外、质谱、核磁等理化分析,得知该化合物与已知化合物Altenusin结构相同.
A high throughput screening method was established for screening AchE inhibitor from fungus. As a result, an active strain, F01-2076 was isolated. The culture broth of it was processed by solvent extraction, SiO2 column chromatography and ODS HPLC purification , then an active compound named F01-2076A was got. The compound showed inhibitory activity against Ache of ICs0 23.4 μmol/L. By means of physicalchemical properties, ^13C-NMR and 1H-NMR analysis, the structure of this compound was identical with the Altenusin. It was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor. The compound is discovered as a Ache inhibitor for the first time.
出处
《河北大学学报(自然科学版)》
CAS
北大核心
2006年第1期47-50,共4页
Journal of Hebei University(Natural Science Edition)
基金
国家科技部创新药物筛选技术平台研究基金项目(2002AA2AZ343D)