Novel 1,3-Benzodioxole From Marine-Derived Actinomycete in East Vietnam Sea

被引:4
作者
Dao Phi Thi [1 ]
Huong Doan Thi Mai [1 ,2 ]
Duc Danh Cao [1 ,2 ]
Quyen Vu Thi [1 ]
Mai Anh Nguyen [1 ]
Hong Minh Le Thi [1 ]
Dang Thach Tran [3 ]
Van Minh Chau [1 ]
Van Cuong Pham [1 ,2 ]
机构
[1] Vietnam Acad Sci & Technol VAST, Adv Ctr Bioorgan Chem, Inst Marine Biochem, Hanoi, Vietnam
[2] Grad Univ Sci & Technol, Dept Chem, VAST, Hanoi, Vietnam
[3] Univ Ind Vinh, Dept Appl Sci & Technol, Vinh, Vietnam
关键词
actinomycete; Streptomyces; benzodioxole; antibacterial; antiyeast; METABOLITES; BACTERIUM; ASSAY;
D O I
10.1177/1934578X20920042
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Analysis of an antimicrobial extract from the culture broth of the marine-derived actinomycete Streptomyces sp. G261 led to the isolation of a new 1,3-benzodioxole derivative (1), together with 10 known compounds 2-11. The actinomycete strain G261 was isolated from sediment, collected at Cu Lao Cham, Quang Nam in Vietnam. The taxonomic identification of the strain G261 was achieved by analysis of 16SrRNA gene sequences. On the basis of morphological and phylogenetic evidence, the actinomycete strain G261 was assigned to the genus Streptomyces. The structures of the isolated compounds were established by their spectral data analysis, including mass spectrometry, 1-dimensional nuclear magnetic resonance (1D-NMR), and 2D-NMR. The structure of 1 was confirmed by comparison of the calculated with experimental C-13 NMR data. Compound 1 exhibited antimicrobial activity against Enterococcus faecalis and Staphylococcus aureus with minimum inhibitory concentration values of 128 and 256 mu g/mL, respectively. Whereas, compound 1 had a weak inhibition when tested against 4 cancer cell lines, KB, LU-1, HepG-2, and MCF-7.
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页数:6
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