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Chemical Constituents of Ainsliaea yunnanensis Franch
Corresponding Author(s) : Xiang-Lei Wu
Asian Journal of Chemistry,
Vol. 32 No. 2 (2020): Vol 32 Issue 2
Abstract
Chemical investigation of the constituents of the whole herb of Ainsliaea yunnanensis Franch has led to isolation of hentriacontane (1), (6Z,9Z)-henicosa-6,9-diene (2), methyl linoleate (3), dodecyl (Z)-9-hexadecenoate (4), heptadecan-8-ol (5), α-linolenic acid (6), (Z)-6-hexadecenoic acid (7), (Z)-10-eicosenoic acid (8), stearic acid (9), phytenoic acid (10), tripalmitolein (11), trilinolenin (12), phthalic acid bis-(2-ethylhexyl) ester (13), diisobutyl phthalate (14), 2-hydroxy-butanedioic acid-4-methyl ester (15), diacylgalactolipids I (16), β-D-galactopyranoside-1,2-bis[(1-oxo-9,12,15-octadecatrienyl)oxy]propyl (17), (2S)-1,2-O-(9Z,12Z-octadecadienoyl)-3-O-[α-D-galactopyranosyl-(1′′′′→6′′′)-O-β-D-galactopyranosyl]glycerol (18). The structures of the compounds were identified by comparison of their NMR data with literature data.
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J.J. Li, B. Zhang, H.L. Liu, X. Zhang, X.Y. Shang and C.Q. Zhao, Molecules, 21, 1481 (2016); https://doi.org/10.3390/molecules21111481.
R. Wang, Z. Sun, A. Li, Z.Z. Yuan, J.J. Li and X.Y. Shang, Chin. Med. Mat., 36, 61 (2013).
X.L. Wu, X.J. Xiong, Z.J. Wu, Y.H. Shen and H. Huang, Guangxi Zhi Wu, 35, 109 (2015).
J.J. Li, A.L. Wang, Z.Z. Yuan, C.Y. Wu, L.H. Yang and X.Y. Shang, China J. Chin. Mater. Med., 38, 3918 (2013);
X. Fang, R.T. Zeng, Z.G. Zhuo, Y.H. Shen and W.D. Zhang, Phytochem. Lett., 26, 25 (2018); https://doi.org/10.1016/j.phytol.2018.05.013.
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J.J. Wang, K.Y. Liu, W.B. Tang, G.Y. He and C.W. Jiang, Lishizhen Med. Mater. Med. Res., 23, 1206 (2012).
A.M. El-Sayed, A.R. Gibb, D.M. Suckling, B. Bunn, S. Fielder, D. Comeskey, L.A. Manning, S.P. Foster, B.D. Morris, T. Ando and K. Mori, J. Chem. Ecol., 31, 621 (2005); https://doi.org/10.1007/s10886-005-2050-5.
Z. Zhu, L. Ma, H.Y. Zhu, X.S. Yang and X.J. Hao, Chin. Med. Mater., 34, 223 (2011).
S. Louw, B.V. Burger, M. Le Roux and J.H. Van Wyk, J. Nat. Prod., 74, 1364 (2011); https://doi.org/10.1021/np1008366.
T. Fujii, R. Yamakawa, Y. Terashima, S. Imura, K. Ishigaki, M. Kinjo and T. Ando, J. Chem. Ecol., 39, 28 (2013); https://doi.org/10.1007/s10886-012-0225-4.
N.N. Kong, S.T. Fang, Y. Liu and C.H. Xia, Chin. Tradit. Herbal Drugs, 44, 3114 (2013).
A.A. Wube, A. Hufner, C. Thomaschitz, M. Blunder, M. Kollroser, R. Bauer and F. Bucar, Bioorg. Med. Chem., 19, 567 (2011); https://doi.org/10.1016/j.bmc.2010.10.060.
M. Xu, J. Wang, Y.P. Chen, S.M. Deng, Z.Y. Liang and R.G. Zheng, Lishizhen Med. Mater. Med. Res., 22, 2643 (2011);
M.H. Chang, G.J. Wang, Y.H. Kuo and C.K. Lee, J. Chin. Chem. Soc., 47, 1131 (2000); https://doi.org/10.1002/jccs.200000152.
L. Retief, J.M. McKenzie and K.R. Koch, Magn. Reson. Chem., 47, 771 (2009); https://doi.org/10.1002/mrc.2463.
L. Mannina, C. Luchinat, M. Patumi, M.C. Emanuele, E. Rossi and A. Segre, Magn. Reson. Chem., 38, 886 (2000); https://doi.org/10.1002/1097-458X(200010)38:10<886::AIDMRC738>3.0.CO;2-J.
X.J. Luo, X.F. Xiao and Z.L. Wang, Chin. Tradit. Herbal Drugs, 40, 190 (2009).
D. Wang, H. Yang, Y.P. Dai, L. Tong and B.C. Cai, Chin. Pharm. J., 43, 1292 (2008).
Y.B. Yang, Y. Yang, X. Li, Z. Yang, Z.J. Wu, Y.L. Zhen and L.N. Sun, Chin. Med. Mater., 32, 1388 (2009).
B.W. Son, J.C. Kim, S.M. Lee, Y.J. Cho, J.S. Choi, H.D. Choi and J.C. Song, Bull. Korean Chem. Soc., 21, 1138 (2000).
X.Y. Chai, C.C. Bai, Y.L. Song, Y.P. Chen, F.F. Li and P.F. Tu, Chin. J. Nat. Med., 6, 179 (2008); https://doi.org/10.3724/SP.J.1009.2008.00179.
L.P. Liu, J.Q. Zhang, X.Y. Wang and H.B. Wang, Nat. Prod. Commun., 7, 1499 (2012).