Arnequinol A and arnequinone A, two unique meroterpenoids from Arnebia euchroma
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* Corresponding author.
E-mail address: pczhang@imm.ac.cn (P.-C. Zhang).
Citation:
Hai-Wei Yan, Rong-Rong Du, Xu Zhang, Ya-Nan Yang, Xiang Yuan, Zi-Ming Feng, Jian-Shuang Jiang, Pei-Cheng Zhang. Arnequinol A and arnequinone A, two unique meroterpenoids from Arnebia euchroma[J]. Chinese Chemical Letters,
;2022, 33(5): 2555-2558.
doi:
10.1016/j.cclet.2021.09.064
N. Kumar, R. Kumar, K. Kishore, Pharmacogn. Rev. 7 (2013) 140-151.
doi: 10.4103/0973-7847.120513
R. Gupta, G.D. Gupta, Pharmacogn. Rev. 9 (2015) 127-131.
doi: 10.4103/0973-7847.162124
M. Moir, R.H. Thomson, J. Chem. Soc. Perkin Trans. I. 13 (1973) 1352-1357.
M.J. Oza, Y.A. Kulkarni, J. Pharm. Pharmacol. 69 (2017) 755-789.
doi: 10.1111/jphp.12715
T.S. Matos, A.K.O. Silva, A.L. Quintela, et al., Fitoterapia 123 (2017) 65-72.
doi: 10.1016/j.fitote.2017.09.021
X.S. Yao, E. Yutaka, N. Hiroshi, et al., Tetrahedron. Lett. 25 (1984) 5541-5542.
doi: 10.1016/S0040-4039(01)81620-8
A.F. Ahmed, H.A. Saad, E.M.A. El-Karim, Molecules 19 (2014) 5940-5951.
doi: 10.3390/molecules19055940
M. Liao, P. Yan, X. Liu, et al., J. Chromatogr. B 1136 (2020) 121924.
doi: 10.1016/j.jchromb.2019.121924
O.D.L. Pessoa, T.L.G. Lemos, M.G. Calvalho, et al., Phytochemistry 40 (1995) 1777-1786.
doi: 10.1016/0031-9422(95)00397-P
G.M. Costa, T.L.G. Lemos, O.D.L. Pessoa, et al., J. Nat. Prod. 62 (1999) 1044-1045.
doi: 10.1021/np980575y
S. Dettrakul, S. Surerum, S. Rajviroongit, et al., J. Nat. Prod. 72 (2009) 861-865.
doi: 10.1021/np9000703
P.P. Painter, B.M. Wong, D.J. Tantillo, Org. Lett. 16 (2014) 4818-4821.
doi: 10.1021/ol5023036
Y. Wang, Y. Zhu, L. Xiao, et al., Fitoterapia 131 (2018) 236-244.
doi: 10.1016/j.fitote.2018.11.005
M. Moir, R.H. Thomson, J. Chem. Soc. Perkin Trans. I 15 (1973) 1556-1561.
K. Mori, M. Kawano, H. Fuchino, et al., J. Nat. Prod. 71 (2008) 18-21.
doi: 10.1021/np070211i
J.M. He, S.C. Sun, Z.L. Sun, et al., Int. J. Antimicrob. Ag. 53 (2019) 70-73.
doi: 10.1016/j.ijantimicag.2018.08.021
H.M. Li, Y.L. Tang, Z.H. Zhang, et al., Planta Med. 78 (2012) 39-45.
doi: 10.1055/s-0031-1280266
L. Wang, F. Li, X. Liu, et al., Planta Med. 81 (2015) 320-326.
doi: 10.1055/s-0035-1545693
H. Cao, W. Zhang, D. Liu, et al., Bioorg. Chem. 96 (2020) 103655.
doi: 10.1016/j.bioorg.2020.103655
A. Kumar, S. Shashni, P. Kumar, et al., J. Ethnopharmacol. 271 (2021) 113896.
doi: 10.1016/j.jep.2021.113896
K. Xu, J.S. Jiang, Z.M. Feng, et al., J. Nat. Prod. 79 (2016) 1567-1575.
doi: 10.1021/acs.jnatprod.6b00066
S. Kim, R. Matsubara, M. Hayashi, J. Org. Chem. 84 (2019) 2997-3003.
doi: 10.1021/acs.joc.8b02961
J. Li, J.K. Liu, W.X. Wang, J. Org. Chem. 85 (2020) 11350-11358.
doi: 10.1021/acs.joc.0c01451
G.D. Manners, L. Jurd, J. Chem. Soc. Perkin Trans. I. 4 (1977) 405-410.
Z.F. Hu, A.D. Gu, L. Liang, et al., Green Chem. 21 (2019) 3286-3299.
doi: 10.1039/C8GC04066D
S.Y. Shao, F. Zhang, Y.N. Yang, et al., Bioorg. Chem. 113 (2021) 105025.
doi: 10.1016/j.bioorg.2021.105025
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