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Two new lignans fromLindera obtusiloba blume

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Abstract

Two new furanolignans (3, 5), together with three known lignans (1, 2, 4), were isolated from the stem ofLindera obtusiloba (Lauraceae). The structures of the compounds were determined as actifolin (1), pluviatilol (2), 5,6-dihydroxymatairesinol (3), (+)-syringaresinol (4), and (+)-9′-O-trans-feruloyl-5,5′-dimethoxylariciresinol (5) on the basis of physicochemical and spectroscopic evidences. Compounds1, 2, 3, and5 showed cytotoxicity against a small panel of human tumor cell lines with ED50 values of 3.40∼19.27 μg/ml.

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References Cited

  • Corrie, J. E. T., Green, G. H. and Taylor, W. C., The chemical constituents of AustralianZanthoxylum species.Aust. J. Chem., 23, 133–145 (1970).

    CAS  Google Scholar 

  • Deyama, T., Ikawa, T., Kitagawa, S. and Nishibe, S., The constituents of Eucommia ulmoides Oliv. V. Isolation of dihydroxydehydrodiconiferyl alcoho isomers and phenolic compounds.Chem. Pharm. Bull., 35, 1785–1789 (1987).

    CAS  Google Scholar 

  • Hsiao, J. J. and Chiang, H. C., Lignans from the wood ofAralia bipinnata.Phytochemistry, 39, 899–902 (1995).

    Article  CAS  Google Scholar 

  • Kinjo, J., Higuchi, H., Fukui, K. and Nohara, T., Lignoids from Albizziae Cortex II. A biodegradation pathway of syringaresinol.Chem. Pharm. Bull., 39, 2952–2955 (1991).

    CAS  Google Scholar 

  • Komae, H. and Hayashi, H., Phytosterols of the trunks ofLindera obtusiloba.Phytochemistry, 11, 1182 (1972).

    Article  CAS  Google Scholar 

  • Macrae, W. D. and Towers, G. H. N., Non-alkaloidal constituents ofVirola elongata Bark.Phytochemistry, 24, 561–566 (1985).

    Article  CAS  Google Scholar 

  • Nishibe, S., Chiba, M. Sakushima, A., Hisada, S., Yamanouchi, S., Takido, M., Sankawa, U. and Sakakibara, A., Introduction of an alcoholic hydroxyl group into 2,3-dibenzylbutyrolactone lignans with oxidizing agents and carbon-13 nuclear magnetic resonance spectra of the oxidation products.Chem. Pharm. Bull., 28, 850–860 (1980).

    CAS  Google Scholar 

  • Niwa, M., Iguchi, M. and Yamamura, S., Three new obtusilactones fromLindera obtusiloba Blume.Chemistry Letters, 655–658 (1975a).

  • Niwa, M., Iguchi, M. and Yamamura, S., The structures of C17-obtusilactone dimer and two C21-obtusilactones.Tetrahedron Letters, 49, 4395–4398 (1975b).

    Article  Google Scholar 

  • Skehan, P., Storeng, R., Scudiero, D., Monks, A., Mc-Mahon, J., Vistica, D., Warren, J. T., Bokesch, H., Kenney, S. and Boyd, M. R., New colorimetric cytotoxicity assay for anticancer-drug screening.J. Natl. Cancer Inst. 82, 1107–1112 (1990).

    Article  PubMed  CAS  Google Scholar 

  • Subbaraju, G. V., Kumar, K. K. K., Raju, B. L. and Pllai, K. R., Justiciresinol, a new furanoid lignan fromJusticia glauca.J. Na. Prod., 54, 1639–1641 (1991).

    Article  CAS  Google Scholar 

  • Taffrout, M., Rouessac, F. and Robin, J.-P., Isolement du prestegane B à partir de Steganotaenia araliacea Hochst., premier lignane bis-(meta-hydroxy-benzyl)-butanolide d'origine vè gè table.Tetrahedron Letters, 25, 4127–4128 (1984).

    Article  Google Scholar 

  • Tanaka, H., Nakamura, T., Ichino, K. and Ito, K., A lignan fromActinodaphne longifolia Phytochemistry, 28, 952–954 (1989).

    Article  CAS  Google Scholar 

  • Tanoguchi, M., Hosono, E., Kitaoka, M., Arimoto, M. and Yamaguchi, H., Studies on the constituents of the seeds ofHernandia ovigera L. IX. Identification of two dibenzylbutyrolactone-type lignans and an attempt of conversion into phenyltetralin-type lignan.Chem. Pharm. Bull., 39, 1873–1876 (1991).

    CAS  Google Scholar 

  • Yook, C. S., Medicinal Plants of Korea. Academy Publishing Co., Seoul, Korea, p.184, 1989.

    Google Scholar 

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Correspondence to Kang Ro Lee.

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Kwon, H.C., Choi, S.U., Lee, J.O. et al. Two new lignans fromLindera obtusiloba blume. Arch Pharm Res 22, 417–422 (1999). https://doi.org/10.1007/BF02979069

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