Three New Lignans, Longipedunins A-C, from Kadsura longipedunculata and Their Inhibitory Activity against HIV-1 Protease

  • Sun Quan-Zhong
    Department of Pharmacognosy, School of Pharmacy, Fudan University
  • Chen Dao-Feng
    Department of Pharmacognosy, School of Pharmacy, Fudan University
  • Ding Pei-Lan
    Department of Pharmacognosy, School of Pharmacy, Fudan University
  • Ma Chao-Mei
    Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University
  • Kakuda Hiroko
    Laboratory of Chemistry, Toyama Medical and Pharmaceutical University
  • Nakamura Norio
    Department of Metabolic Engineering, Institute of Natural Medicine, Toyama Medical and Pharmaceutical University
  • Hattori Masao
    Department of Metabolic Engineering, Institute of Natural Medicine, Toyama Medical and Pharmaceutical University

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抄録

Three new lignans, longipedunins A (1), B (2) and C (3), together with three known compounds, benzoyl-binankadsurin A (4), acetyl-binankadsurin A (5) and schisanlactone A (6), were isolated from Kadsura longipedunculata. Their structures and stereochemistry were determined by spectral and single-crystal X-ray analyses. Compounds 1 and 6 showed appreciable inhibitory activity against HIV-1 protease with IC50 values of 50 and 20 μM, respectively.

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