Citation: Yan-Xia Zhang, Bing Xia, Yan Zhou, Li-Sheng Ding, Shu-Lin Peng. Two new cyclic diarylheptanoids from the stems of Ostryopsis nobilis[J]. Chinese Chemical Letters, ;2013, 24(6): 512-514. shu

Two new cyclic diarylheptanoids from the stems of Ostryopsis nobilis

1.
Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China

Corresponding author: Shu-Lin Peng,
Received Date: 27 November 2012
Available Online: 28 February 2013

Two new cyclic diarylheptanoids named ostryopsitrienol (1) and ostryopsitriol (2), together with six known compounds, were isolated from the stems of endemic medicinal plant of Ostryopsis nobilis (Betulaceae). The structures of the new compounds were elucidated by means of HRMS, ¹D NMR, ²DNMR and X-ray crystallography analysis.
- Ostryopsis nobilis,
- Cyclic diarylheptanoid,
- Ostryopsitrienol,
- Ostryopsitriol
1. [1]
  [1] T.S. Ying, Y.L. Zhang, D.E. Boufford, The Endemic Genera of Seed plants of China, Science Press, Beijing, 1993, p. 230.
2. [2]
  [2] H.Y. Ye, C.X. Chen, X.J. Hao, The chemical constituents from Ostryopsis nobilis, Acta Bot. Yunnanica 18 (1996) 473-475.
3. [3]
  [3] M.W. Lee, T. Tanaka, G.I. Nonaka, et al., Phenolic compounds on the leaves of Betula platyphylla var. latifolia, Arch. Pharm. Res. 15 (1992) 211-214.
4. [4]
  [4] Y. Akihito, M. Yoshihiro, S. Hiroshi, S. Yutaka, New diarylheptanoids and diarylheptanoid glucosides from the rhizomes of Tacca chantrieri and their cytotoxic activity, J. Nat. Prod. 65 (2002) 283-289.
5. [5]
  [5] H. Fuchino, T. Satoh, N. Tanaka, Chemical evaluation of Betula species in Japan. Ⅲ. Constituents of Betula maximowicziana, Chem. Pharm. Bull. 44 (1996) 1748-1753.
6. [6]
  [6] D. Smati, A. Longeon, M. Guyot, 3b-(3,4-Dihydroxycinnamoyl)-erythrodiol, a cytotoxic constituent of Zygophyllum geslini collected in the Algerian Sahara, J. Ethnopharmacol. 95 (2004) 405-407.
7. [7]
  [7] Y. Zhang, Y. Liu, D. Meng, X. Li, Spectral characteristics of cyclic diarylheptanoids, Chin. J. Magn. Reson. 27 (2010) 669-677.
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