1. Academic Validation
  2. Bioactive Limonoid Constituents of Munronia henryi

Bioactive Limonoid Constituents of Munronia henryi

  • J Nat Prod. 2015 Apr 24;78(4):811-21. doi: 10.1021/np501057f.
Ying Yan 1 2 Jian-Xin Zhang 1 Tao Huang 1 Xin-Ying Mao 1 Wei Gu 1 Hong-Ping He 3 Ying-Tong Di 3 Shun-Lin Li 3 Duo-Zhi Chen 3 Yu Zhang 3 Xiao-Jiang Hao 1
Affiliations

Affiliations

  • 1 †The Key Laboratory of Chemistry for Natural Products of Guizhou Province and Chinese Academy of Sciences, Guiyang 550002, People's Republic of China.
  • 2 ‡Center for Research and Development of Fine Chemicals, Guizhou University, Guiyang 550025, People's Republic of China.
  • 3 §State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, People's Republic of China.
Abstract

Fourteen new limonoids, munronins A-N (1-14), and eight known limonoids (15-22) were isolated from the whole Plants of Munronia henryi. The structures of the new compounds were elucidated by 2D NMR spectroscopy and mass spectrometry, and the structure of 8 was confirmed by single-crystal X-ray diffraction analysis. Compound 1 represents the first limonoid found with a novel 7-oxabicyclo[2.2.1]heptane moiety produced by incorporating C-11 and C-14 via an oxygen atom. All compounds were evaluated for their anti-tobacco mosaic virus (TMV) activity and in vitro cytotoxicity against the human Cancer HL-60, SMMC-7721, A-549, MCF-7, and SW-480 cell lines. Among them, compounds 2, 8, 9, 10, 11, 12, 18, and 20 showed significant anti-TMV activity, with IC50 values in the range 19.6-44.4 μg/mL. Compounds 1 and 18 exhibited cytotoxic effects for all five Cancer cell lines, with IC50 values between 0.4 and 4.8 μM.

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