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http://dx.doi.org/10.5012/jkcs.2010.54.6.701

Chemical Constituents of the Halophyte Glehnia littoralis  

Um, Young-Ran (Center for Herbal Medicine Improvement Research, Korea Institute of Oriental Medicine)
Lee, Jung-Im (Division of Marine Environment and Bioscience, Korea Maritime University)
Lee, Jin-Hyeok (Division of Marine Environment and Bioscience, Korea Maritime University)
Kim, Hae-Jin (Division of Marine Environment and Bioscience, Korea Maritime University)
Yea, Sung-Su (Department of Biochemistry, College of Medicine, Inje University)
Seo, Young-Wan (Division of Marine Environment and Bioscience, Korea Maritime University)
Publication Information
Abstract
Two polyacetylenes (1 and 2), four coumarins (3-6), and one sesquiterpene (7) were isolated from the halophyte Glehnia littoralis. Particularly, compound 6 and 7 were isolated for the first time from Glehnia littoralis. Their chemical structures have been determined by extensive 2-D NMR experiments such as $^1H$, COSY, HMQC and HMBC and by comparison with the reported data in the literature.
Keywords
Halophyte; Glehnia littoralis; Coumarin; Polyacetylene; Sesquiterpene;
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1 Um, Y. R.; Kong, C. S.; Lee, J. I.; Kim, Y. A.; Nam, T. J.; Seo, Y. W. Process Biochemistry 2010, 45, 114.   DOI
2 Elgmal, M. H. A.; Elewa, N. H.; Elkhrisy, E. A. M.; Duddck, H. Phytochem. 1979, 18, 139.   DOI
3 Masuda, T.; Takasugi, M.; Anetai, M. Phytochem. 1998, 47, 13.   DOI
4 Lechner, D.; Stavri, M.; Oluwatuyi, M.; Pereda-Miranda. R.; Gibbons, S. Phytochem. 2004, 65, 331.   DOI
5 Lee, J. H.; Kim, K. H. Cancer Prev. Res. 2008, 13, 216.
6 Repcak, M.; Imrich, J.; Franekova, M. J. Plant Physiol. 2001, 158, 1085.   DOI
7 Singh, R.; Singh, B.; Singh, S.; Kumar, N.; Kumar, S.; Arora, S. Food Chem. 2010, 120, 825.   DOI   ScienceOn
8 Hirata, T.; Shimoda, K.; Fujino, T.; Ohta, S. J. Mol. Catal. B Enzym. 2000, 10, 477.   DOI
9 Bayoumi, S. A. L.; Rowan, M. G.; Beeching, J. R.; Blagbrough, I. S. Phytochem. 2010, 71, 598.   DOI
10 Mikami, M.; Taya, S.; Nakai, T.; Fujita, Y. J. Org. Chem. 1981, 46, 5449.   DOI
11 Spraul, M. H.; Nitz, S.; Drawert, F.; Duddeck, H.; Hiegemann, M.; Phytochem. 1992, 31, 3109.   DOI
12 Appendino, G.; Jakupovic, J.; Bossio, E. Phytochem. 1998, 49, 1719.   DOI
13 Li, H. I.; Liu, T. S.; Huang, T. C.; Koyama, T.; Devol, C. E. Flora of Taiwan, vol. 3; National Taiwan University, Ed. National Science Council of the Republic of China Press: Taipei, Taiwan, 1977, pp 951-952.
14 Chiang Su New Medicinal College (de.). Dictionary of Chinese Crude Drug; Shanghai Scientific Technologic Publisher: Shanghai, 1977, p 644.
15 Choo, B. K.; Ji, Y. U.; Moon, B. C.; Kim, B. B.; Lee, A. Y.; Yoon, T. S.; Song, H. K.; Kim, H. K. J. Korean Env. Res. & Reveg. Rech. 2008, 11, 38.
16 Kim, S. M.; Shin, D. I.; Song, H. S.; Kim, S. K.; Yoon, S. T. Korean J. Medicinal Crop Sci. 2005, 13, 171.
17 Hiraoka, N.; Chang, J. I.; Bohm, L. R.; Bohm, B. A, Biochem Syst Ecol. 2002, 30, 321.   DOI
18 Miyazawa, M.; Kurose, K.; Itoh, A.; Hiraoka, N.; Kameoka, H. Flavour Fragr. J. 2001, 16, 215.   DOI
19 Shin, S. W. Natural product sciences. 2005, 11, 92.
20 Anetai, M.; Masuda, T.; Takasugi, M. Natural Medicines 1996, 50, 399.
21 Anetai, M.; Masuda, T.; Takasugi, M. Natural Medicines 1997, 51, 442.
22 Kong, C. S.; Um, Y. R.; Lee, J. I.; Kim, Y. A.; Ye, S. S.; Seo, Y. W. Food Chem. 2010, 120, 385.   DOI
23 Seo, Y. K.; Ryu, K. S. Korean J. Pharmacog. 1977, 7, 233.