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Chemical Constituents of the Barks of Litsea rubescens

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A phytochemical investigation of the ethanol extract from the barks of Litsea rubescens resulted in the isolation of three new compounds, 3α,7β-diacetyl-8β-methyloctahydro-4β-methyl formate (1), (–)-N-methoxycarbonylorientailine (3), and 9-O-[4-O-acetyl-α-L-rhamnopyranosyl-(1→6)-β-Dglucopyranosyl]-3,4-dimethoxycinnamic acid (5), together with two known compounds, 3α,7β-dihydroxy-8β-methyloctahydro-4β-methyl formate (2) and (–)-orientailine (4). The structures of the three new compounds were elucidated on the basis of 1D, 2D NMR (COSY, HMQC, HMBC, and NOESY), and mass spectral analyses.

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References

  1. X. H. Yan, F. X. Zhang, H. H. Xie, and X. Y. J. Wei, Trop. Subtrop. Bot., 2, 171 (2000).

    Google Scholar 

  2. K. A. B. S. da Silva, L. C. Klein-Junior, S. M. Cruz, A. Caceres, N. L. M. Quintao, F. D. Monache, and V. Cechinel-Filho, Food Chem., 132, 1980 (2012).

    Article  Google Scholar 

  3. D. G. Kong, Y. Zhao, G. H. Li, B. J. Chen, X. N. Wang, H. L. Zhou, H. X. Lou, D. M. Ren, and T. Shen, J. Ethnopharmacol., 164, 256 (2015).

    Article  CAS  PubMed  Google Scholar 

  4. W. J. Tang, Y. L. Zhang, Q. P. Xiao, C. Huang, Y. Jin, and J. Li, Chem. Biodiv., 10, 1128 (2013).

    Article  CAS  Google Scholar 

  5. R. C. Rastogi and N. Borthakur, Phytochemistry, 19, 998 (1980).

    Article  CAS  Google Scholar 

  6. J. A. Lopez, W. Barillas, and G. L. Jorge, Planta Med., 61, 198 (1995).

    Article  CAS  PubMed  Google Scholar 

  7. E. H. Hakim, S. A. Achmad, M. Effendy, E. L. Ghisalberti, D. C. R. Hockless, and A. H. White, Aust. J. Chem., 46, 1355 (1993).

    Article  CAS  Google Scholar 

  8. S. A. Achmad, E. L. Ghisalberti, E. H. Hakim, L. Makmur, and M. Mamurung, Phytochemistry, 31, 2153 (1992).

    Article  CAS  Google Scholar 

  9. H. Tanaka, T. Nakamura, K. Ichino, K. Ito, and T. Tanaka, Phytochemistry, 29, 857 (1990).

    Article  CAS  Google Scholar 

  10. K. P. Padmakumari and C. S. J. Narayannan, Essent. Oil Res., 4, 87 (1992).

    Article  CAS  Google Scholar 

  11. L. Li, X. T. Zhao, Y. P. Luo, J. F. Zhao, X. D. Yang, and H. B. Zhang, Bioorg. Med. Chem. Lett., 21, 7431 (2011).

    CAS  PubMed  Google Scholar 

  12. H. Corrode and E. Hardegger, Helv. Chim. Acta, 39, 889 (1956).

    Article  Google Scholar 

  13. J. Kunitomo, Yakugaku Zasshi, 81, 1253 (1972).

    Article  Google Scholar 

  14. S. Hara, H. Okabe, and K. Mihashi, Chem. Pharm. Bull., 35, 501 (1987).

    Article  CAS  Google Scholar 

  15. Y. Zhang, Y. J. Zhang, M. R. Jacob, X. C. Li, and C. R. Yang, Phytochemistry, 69, 264 (2008).

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Jiang Hu.

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Published in Khimiya Prirodnykh Soedinenii, No. 4, July–August, 2017, pp. 591–594.

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Hu, J., Mao, X., Shi, X. et al. Chemical Constituents of the Barks of Litsea rubescens . Chem Nat Compd 53, 694–697 (2017). https://doi.org/10.1007/s10600-017-2093-1

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  • DOI: https://doi.org/10.1007/s10600-017-2093-1

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