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New Alkaloids and Steroids from Hydranth of Goniopora columna Corals and Their Inhibiting Lung Cancer Cell Activities.
Feng, Guangfu; He, Jieyi; Li, Qiqi; Bai, Meng; Liu, Kai; Liu, Xinming; Yi, Xiangxi; Liu, Yonghong; Luo, Lianxiang; Gao, Chenghai.
Affiliation
  • Feng G; Institute of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • He J; Guangxi Key Laboratory of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Li Q; The Marine Biomedical Research Institute, Guangdong Medical University, Wenming East-Road 2, 524023, Zhanjiang, Guangdong, China.
  • Bai M; The Marine Biomedical Research Institute of Guangdong Zhanjiang, Wenming East-Road 2, 524023, Zhanjiang, Guangdong, China.
  • Liu K; Institute of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Liu X; Guangxi Key Laboratory of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Yi X; Institute of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Liu Y; Guangxi Key Laboratory of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Luo L; Institute of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
  • Gao C; Guangxi Key Laboratory of Marine Drugs, Guangxi University of Chinese Medicine, Wuhe Road 13, 530200, Nanning, China.
Chem Biodivers ; 21(4): e202301993, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38342755
ABSTRACT
A new alkaloids, aplysingoniopora A (1), and new configuration pregnane type steroid compound, 9,17-α-pregn-1,4,20-en-3-one (2), and two known pregnane type steroid compounds (3 and 4) were isolated from hydranth of Goniopora columna corals. The compounds structures and absolute configurations were determined by extensive spectroscopic analysis, MS data, single-crystal X-ray diffraction analysis and quantum chemical calculation. The anticancer effect of the compounds were explored in human non-small-cell lung cancer (NSCLC) A549 cell lines. As the results, the compound 3 and 4 induces toxicity and has proliferation inhibitory effects on A549 cells (IC50=58.99 µM and 58.77 µM, respectively) in vitro.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Anthozoa / Alkaloids / Lung Neoplasms Limits: Animals / Humans Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Anthozoa / Alkaloids / Lung Neoplasms Limits: Animals / Humans Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland