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作 者:姜威[1] 金文藻[1] 张月琴[1] 魏玉珍[1]
机构地区:[1]中国医学科学院中国协和医科大学医药生物技术研究所
出 处:《中国抗生素杂志》1998年第4期263-266,共4页Chinese Journal of Antibiotics
基 金:自然科学基金
摘 要:在寻找微生物活性代谢产物的过程中,发现东北红豆杉内生真菌TCH68的发酵液能够使细胞有丝分裂停止在中期,从其培养物中分离得到2个新化合物TCH68-1和TCH68-2。经光谱分析确定TCH68-1的结构为2,5-dioxo-3-methyl-8,9,10-trimethoxy-9-chloro-1,106,8-dilactone。TCH68-2的结构为2-[(Z)-1-oxo-2,3-dihydroxy-4-heptenyl]-2-ene-3-methyl-4-oxo-5-hydroxy-6-methoxy-6-benzoyl-ε-caprolactam。During the course of searching for microbial active metabolites, the fermentation broth of hyphomycete TCH68, an endophytic fungus associated with the inner bark of Taxus cuspidata Sieb. et Zucc., was found to induce mitotic arrest in vitro. Two novel compounds, TCH681 and TCH682 have been isolated from the culture by silica gel column chromatography and preparative TLC. Based on spectral data, including UV, IR, FAB-MS, HREI-MS, ~1 HNMR, ^(13)CNMR, DEPT, 1H1H COSY, HETCOR and HMBC, the structures of TCH681 and TCH682 have been assigned as 2, 5-dioxo-3-methyl-8, 9, 10-trimethoxy-9-chloro-1, 10∶6, 8-dilactone and 2-[(Z)-1-oxo-2, 3-dihydroxy-4-heptenyl]-2-ene-3-methyl-4-oxo-5-hydroxy-6-methoxy-6-benzoylεcaprolactam respecitively.
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