期刊
ORGANIC LETTERS
卷 19, 期 16, 页码 4207-4210出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01807
关键词
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资金
- Japan Society for the Promotion of Science [17K13261, 15K08013]
- Grants-in-Aid for Scientific Research [15K06888, 17K13261, 15K08013] Funding Source: KAKEN
New 36-membered polyol macrolides deplelides A and B were isolated from the culture of Streptomyces MM581-NF15 by bioassay-guided fractionation using an ATP depletion assay. The planar structures of these novel compounds were identified by interpretation of the spectroscopic data (1D/2D NMR, MS, and IR). The relative stereochemistry was partially established using the universal NMR database method and J-based configuration analysis using (HH)-H-1-H-1 and long-range (HC)-H-1-C-13 coupling constants determined by H-1 NMR or E.COSY and J-resolved HMBC analysis or another HMBC-based technique, respectively. The absolute stereochemistry was partially determined by a modified Moshers method. These new compounds displayed highly potent ATP depletion activities (IC50 33 nM) and antiproliferative activities against several tumor cell lines, such as HGC-27 (IC50 47 nM).
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