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LIU Meng-Yu-Jie, LI Shan-Ren, LU Chun-Hua. 17-[16,17-Dihydroxycyclooctatinyl]-hexaketide ester from Streptomyces sp. SR107[J]. 中国天然药物, 2016, 14(12): 931-933.
引用本文: LIU Meng-Yu-Jie, LI Shan-Ren, LU Chun-Hua. 17-[16,17-Dihydroxycyclooctatinyl]-hexaketide ester from Streptomyces sp. SR107[J]. 中国天然药物, 2016, 14(12): 931-933.
LIU Meng-Yu-Jie, LI Shan-Ren, LU Chun-Hua. 17-[16,17-Dihydroxycyclooctatinyl]-hexaketide ester from Streptomyces sp. SR107[J]. Chinese Journal of Natural Medicines, 2016, 14(12): 931-933.
Citation: LIU Meng-Yu-Jie, LI Shan-Ren, LU Chun-Hua. 17-[16,17-Dihydroxycyclooctatinyl]-hexaketide ester from Streptomyces sp. SR107[J]. Chinese Journal of Natural Medicines, 2016, 14(12): 931-933.

17-16,17-Dihydroxycyclooctatinyl-hexaketide ester from Streptomyces sp. SR107

17-16,17-Dihydroxycyclooctatinyl-hexaketide ester from Streptomyces sp. SR107

  • 摘要: A new hexaketide acid esterified by the 17-hydroxyl group of 16,17-dihydroxycyclooctatin, namely 17-16,17-dihydroxycyclooctatinyl-hexaketide ester (1), a member of the group of rare bacterial diterpenes with a fused 5-8-5 ring system was isolated from strain Streptomyces sp. SR107. The structure was determined on the basis of its spectral data (1H NMR, 13C NMR, 1H-1H COSY, HSQC, HMBC, NOESY, IR and HR-ESI-MS). The antibacterial activity was also evaluated in this paper.

     

    Abstract: A new hexaketide acid esterified by the 17-hydroxyl group of 16,17-dihydroxycyclooctatin, namely 17-16,17-dihydroxycyclooctatinyl-hexaketide ester (1), a member of the group of rare bacterial diterpenes with a fused 5-8-5 ring system was isolated from strain Streptomyces sp. SR107. The structure was determined on the basis of its spectral data (1H NMR, 13C NMR, 1H-1H COSY, HSQC, HMBC, NOESY, IR and HR-ESI-MS). The antibacterial activity was also evaluated in this paper.

     

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