期刊
PLANTA MEDICA
卷 84, 期 3, 页码 201-207出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0043-119888
关键词
angucycline glycoside; naphthacenequinone; cytotoxicity; marine actinomycete; Streptomyces lusitanus; Streptomycetaceae
资金
- National Science Foundation of China [41476133]
- Natural Science Program of Guangdong Province [2016A030313588]
- Science and Technology Projects of Guangdong Province [2013B021100021]
- Projects of Guangdong Provincial Oceanic and Fishery Administration [A201401C05]
- special financial fund of innovative development of marine economic demonstration project [GD2012-D01-001]
- Fund of the Education Bureau of Guangzhou City [1201610155]
- High-Level University Construction Program of Guangdong Province and Guangzhou City
Three new angucycline glycosides, designated grincamycin I ( 1 ), J ( 2 ), and K ( 3 ), together with the known congener A-7884 ( 4 ), were isolated from marine-derived actinomycete Streptomyces lusitanus SCSIO LR32. The structures of the new compounds were elucidated by comprehensive spectral data analysis. Compounds 2 and 4 exhibited antitumor activity against human cancer cells MDA-MB-435, MDA-MB-231, NCI-H460, HCT-116 and HepG2, and human normal breast epithelial cell MCF10A with IC (50) values ranging from 0.4 to 6.9 mu M. In addition, A-7884 ( 4 ) demonstrated antimicrobial activity against Micrococcus luteus with an MIC value of 1.95 mu g/mL.
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