Abstract
With the bioactivity-guided method, a new flavanone glycoside, together with nine known flavonoids were isolated from 50% aqueous ethanol of litchi(Litchi chinensis Sonn.) seeds. The chemical structure of the new compound was elucidated via 1D and 2D nuclear magnetic resonance(NMR) techniques and mass spectrometry to be (2S)-pinocembrin-7-O-(6″-O-α-L-arabinosyl-β-D-glucopyranoside)(1), and the nine known compounds were determined to be quercetin(2), phlorhizin(3), pinocembrin-7-O-glucoside(4), kaempferol-7-O-β-D-glucopyranoside(5), onychin(6), nairutin(7), narcissin(8), pinocembrin-7-O-[(6″-O-β-D-glucopyranoside)-β-D-glucopyranoside](9) and pinocembrin-7-O-[(2″,6″-di-O-α-L-rhamnopyranosyl)-β-D-glucopyranoside](10). Some of the isolated flavonoids were tested for their inhibitory effects on α-glucosidase. And compounds 2 and 3 showed stronger inhibitory activity than positive control.
Similar content being viewed by others
References
Liu Y. Q., Pi Z. F., Song F. R., Liu Z. Q., Liu Z. Y., Chem. J. Chinese Universities, 2012, 33(9), 1932
Pogano G., Marena S., Corgiat-Mansin L., Cravero F., Giorda C., Bozza M., Rossi C. M., Diabetes and Metabolism, 1995, 21(3), 162
Murai A., Iwamura K., Takada M., Ogawa K., Usui T., Okumura J., Life Science, 2002, 71(12), 1405
Lebovitz H. E., Endocrinology and Metabolism Clinics of North America, 1997, 26(3), 539
Holman R. R., Diabetes Research and Clinical Practice, 1998, 40(Suppl. 1), S21
Niwa T., Doi U., Osawa T., Journal of Agricultural and Food Chemistry, 2003, 51(1), 90
Mcdougall G. J., Shpiro F., Doboson P., Smith P., Black A., Stewart D., Journal of Agricultural and Food Chemistry, 2005, 53(7), 2760
Fang J., Li Y. P., Liang W. H., Dong D. C., Liu Y. Q., World Agriculture, 2007, 3, 46
Guo J. W., Pan J. Q., Qiu G. Q., Li A. H., Xiao L. Y., Han C., Chinese Journal of New Drugs, 2003, 12(7), 526
Yang Y. J., Liang B. M., Guangdong Pharmaceutical Journal, 2004, 14(6), 13
Liu Y. G., Pharmaceutical Composition Containing a Safe Extracts of Fruits and Vegetables for the Treating and Preventing of Diabetes, US 4985248, 1991
Hanawa F., Yamada T., Nakashima T., Phytochemistry, 2001, 57(2), 223
Li M. M., Wang K., Pan Z. H., Chen X. Q., Peng L. Y., Cheng X., Zhao Q. S., Chem. Pharm. Bull., 2009, 57(10), 1123
Zeng H. B., Zeng R. J., Yao F., Journal of Hunan Institute of Engineering, 2010, 20(2), 60
Liu H. W., Yao X. S., Chinese Journal of Medicinal Chemistry, 2001, 1, 52
Feng H., Wang Z. M., Dong G. Y., Wu Z., China Journal of Chinese Material Medica, 2001, 26(4), 260
Markham K. R., Ternam B., Stanley R., Geiger H., Mabry T. J., Tetrahedron, 1978, 34(9), 1389
Xu Y. L., Zheng X., He Y. N., Acta Botanica Yunnanica, 1999, 21(4), 497
Yan H. Y., Studies on Chemical Constituents of Oxytropis Falcata Bunge and Cleroderdrun Bugei Stued, Northwest Normal University, Xi’an, 2007
Lü M., Su Y. F., Gao Y., Song D. B., Gao X. M., Zhang B. L., Chinese Traditional and Herbal Drugs, 2009, 40(3), 356
Tomimori T., Imoto Y., Ishida M., Kizu H., Namba T., Journal of the Pharmaceutical Society of Japan, 1998, 42(1), 98
Xu X. Y., Xie H. H., Jiang Y. M., Wei X. Y., Journal of Agricultural and Food Chemistry, 2011, 59, 1205
Kim Y. M., Wang M. H., Rhee H. I., Carbohydr. Res., 2004, 339, 715
Author information
Authors and Affiliations
Corresponding author
Additional information
Supported by the National Natural Science Foundation of China(No.30873370) and the Doctor Fund of Jilin Agricultural University of China(No.201210).
Rights and permissions
About this article
Cite this article
Ren, S., Xu, Dd., Gao, Y. et al. Flavonoids from litchi(Litchi chinensis Sonn.) seeds and their inhibitory activities on α-glucosidase. Chem. Res. Chin. Univ. 29, 682–685 (2013). https://doi.org/10.1007/s40242-013-3030-x
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s40242-013-3030-x