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HAN Bing, LI Wen-Xin, CUI Cheng-Bin. Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest[J]. 中国天然药物, 2015, 13(6): 467-470.
引用本文: HAN Bing, LI Wen-Xin, CUI Cheng-Bin. Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest[J]. 中国天然药物, 2015, 13(6): 467-470.
HAN Bing, LI Wen-Xin, CUI Cheng-Bin. Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest[J]. Chinese Journal of Natural Medicines, 2015, 13(6): 467-470.
Citation: HAN Bing, LI Wen-Xin, CUI Cheng-Bin. Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest[J]. Chinese Journal of Natural Medicines, 2015, 13(6): 467-470.

Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest

Pteridic acid hydrate and pteridic acid C produced by Streptomyces pseudoverticillus YN17707 induce cell cycle arrest

  • 摘要: The present study aimed at identifying cell cycle inhibitors from the fermentation broth of Streptomyces pseudoverticillus YN17707. Activity-guided isolation was performed on tsFT210 cells. Compounds were isolated through various chromatographic methods and elucidated by spectroscopic analyses. Flow cytometry was used to evaluate the cell cycle inhibitory activities of the fractions and compounds. Two compounds were obtained and identified as pteridic acid hydrate (1) and pteridic acid C (2), which arrested the tsFT210 cells at the G0/G1 phase with the MIC values being 32.8 and 68.9 molL-1, respectively. These results provide a basis for future development of Compounds 1 and 2 as novel cell cycle inhibitors for cancer therapy.

     

    Abstract: The present study aimed at identifying cell cycle inhibitors from the fermentation broth of Streptomyces pseudoverticillus YN17707. Activity-guided isolation was performed on tsFT210 cells. Compounds were isolated through various chromatographic methods and elucidated by spectroscopic analyses. Flow cytometry was used to evaluate the cell cycle inhibitory activities of the fractions and compounds. Two compounds were obtained and identified as pteridic acid hydrate (1) and pteridic acid C (2), which arrested the tsFT210 cells at the G0/G1 phase with the MIC values being 32.8 and 68.9 molL-1, respectively. These results provide a basis for future development of Compounds 1 and 2 as novel cell cycle inhibitors for cancer therapy.

     

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