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New Acyclic Triterpenoid Glycoside Constituent from the Fruits of Lycium chinense
Corresponding Author(s) : Ateeque Ahmad
Asian Journal of Chemistry,
Vol. 26 No. 18 (2014): Vol 26 Issue 18
Abstract
One new acyclic triterpenoid constituent as 14,18,22-trimethyl 3a,5a,17a,19a,22a- pentahydroxytetracosan-25,26,27-trioic acid-3a-O-a-L-glucofuranosyl-(6a®1'a)-O-a-L-glucopyranosyl-(6'a®1''a)-O-a-L-glucopyranoside-5a-O-a-L-glucofuranosyl-(6b®1'b)-O-a-L-glucopyranosyl-(6'b®1''b)-glucopyranoside-17a-O-L-glucopyranosyl-(6c®1'c)-O-Lglucopyranosyl-(6'c®1''c)-O-L-glucopyranoside-19a-O-L-glycopyranosyl-(6d®1'd)-O-a-L-glucopyranosyl-(6'd®1''d)-O-a-L-glucopyranoside (1) was isolated and identified from the fruits of Lycium chinense. The chemical structure of the new compound was elucidated by 1D and 2D NMR spectroscopic techniques (COSY, HMBC and HSQC) aided by FAB mass and IR spectra.
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- Y. Peng, C. Ma, Y. Li, K.S.Y. Leung, Z.H. Jiang and Z. Zhao, Plant Foods Hum. Nutr., 60, 161 (2005); doi:10.1007/s11130-005-9550-5.
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References
Y. Peng, C. Ma, Y. Li, K.S.Y. Leung, Z.H. Jiang and Z. Zhao, Plant Foods Hum. Nutr., 60, 161 (2005); doi:10.1007/s11130-005-9550-5.
Pharmacopoeia of the People's Republic of China, Chemical Industry Press, Beijing (2000).
O. Potterat, Planta Med., 76, 7 (2010); doi:10.1055/s-0029-1186218.
S. Funayama, K. Yoshida, C. Konno and H. Hikino, Tetrahedron Lett., 21, 1355 (1980); doi:10.1016/S0040-4039(00)74574-6.
J. Yamahara, M. Kim, T. Sawada and H. Fujimua, Shoyakugaku Zasshi, 18, 33 (1964).
S.Y. Kim, Y.H. Choi, H. Huh, J. Kim, Y.C. Kim and H.S. Lee, J. Nat. Prod., 60, 274 (1997); doi:10.1021/np960670b.
M. Noguchi, K. Mochida, T. Shingu, M. Kozuka and K. Fujitani, Chem. Pharm. Bull. (Tokyo), 32, 3584 (1984); doi:10.1248/cpb.32.3584.
K. Jung, Y.W. Chin, Y.C. Kim and J. Kim, Arch. Pharm. Res., 28, 1381 (2005); doi:10.1007/BF02977905.
Y.G. Shin, K.H. Cho, J.M. Kim, M.K. Park and J.H. Park, J. Chromatomatogr. A, 857, 331 (1999); doi:10.1016/S0021-9673(99)00720-7.
D.G. Lee, H.J. Jung and E.R. Woo, Arch. Pharm. Res., 28, 1031 (2005); doi:10.1007/BF02977397.
N. Asano, A. Kato, M. Miyauchi, H. Kizu, T. Tomimori, K. Matsui, R.J. Nash and R.J. Molyneux, Eur. J. Biochem., 248, 296 (1997); doi:10.1111/j.1432-1033.1997.00296.x.
Z. Zhang, X. Liu, T. Wu, J. Liu, X. Zhang, X. Yang, M.J. Goodheart, J.F. Engelhardt and Y. Wang, Cell Biol. Toxicol., 27, 107 (2011); doi:10.1007/s10565-010-9174-2.
C.C. Wang, S.C. Chang, B.S. Inbaraj and B.H. Chen, Food Chem., 120, 184 (2010); doi:10.1016/j.foodchem.2009.10.005.
Y.W. Chin, S.W. Lim, S.H. Kim, D.Y. Shin, Y.G. Suh, Y.B. Kim, Y.C. Kim and J. Kim, Bioorg. Med. Chem. Lett., 13, 79 (2003); doi:10.1016/S0960-894X(02)00846-6.
S. Yahara, C. Shigeyama, T. Ura, K. Wakamatsu, T. Yasuhara and T. Nohara, Chem. Pharm. Bull. (Tokyo), 41, 703 (1983); doi:10.1248/cpb.41.703.
X.M. Peng and G.Y. Tian, Carbohydr. Res., 331, 95 (2001); doi:10.1016/S0008-6215(00)00321-9.
G.-Q. Zheng, Z.-Y. Zheng, X. Xu and Z.-H. Hu, Biochem. Syst. Ecol., 38, 275 (2010); doi:10.1016/j.bse.2010.01.008.
X.M. Li, X.L. Li and A.G. Zhou, Eur. Polym. J., 43, 488 (2007); doi:10.1016/j.eurpolymj.2006.10.025.
M. Ming, L. Guanhua, Y. Zhanhai, C. Guang and Z. Xuan, Food Chem., 113, 872 (2009); doi:10.1016/j.foodchem.2008.03.064.
W.-S. Jung, I.-M. Chung, M. Ali and A. Ahmad, J. Asian Nat. Prod. Res., 14, 301 (2012); doi:10.1080/10286020.2011.653346.
I.-M. Chung, M. Ali, E.-H. Kim and A. Ahmad, J. Asian Nat. Prod. Res., 15, 136 (2013); doi:10.1080/10286020.2012.756315.
X.-N. Li, C. Chu, S.-Q. Tong, D.-P. Cheng and J.-Z. Yan, Nat. Prod. Res., 27, 750 (2013); doi:10.1080/14786419.2012.698408.