期刊
JOURNAL OF NATURAL PRODUCTS
卷 85, 期 6, 页码 1617-1625出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.2c00279
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资金
- National Natural Science Foundation of China [22177016]
- Natural Science Foundation of Chongqing [cstc2020jcyj-msxmX0537]
- Fundamental Research Funds for the Central Universities [2020CDJ-LHZZ-006]
- State Key Laboratory of Bioactive Substance and Function of Natural Medicines [GTZK201901]
Nine new complex flavanones, named cryptometcones A-I (1-9), along with four known analogues, were isolated from Cryptocarya metcalfiana. Their structures and absolute configurations were determined through spectroscopic data analysis and ECD calculations. Compounds 3-5, 8, and 9 exhibited cytotoxicity against the HCT-116 cancer cell line.
Nine new complex flavanones, cryptometcones A-I (1-9), along with four known analogues, were isolated from Cryptocarya metcalfiana. The structures of 1-9 including their absolute configurations were elucidated by spectroscopic data analysis and electronic circular dichroism (ECD) calculations. In addition, the structure of oboflavanone A was revised, while the absolute configurations of oboflavanone B, cryptoflavanone C, and cryptoflavanone D were determined, according to their spectroscopic data. Compounds 3-5, 8, and 9 exhibited cytotoxicity against the HCT-116 cancer cell line.
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