[1] Lu, Y.; Chen, D.F. Analysis of Schisandra chinensis and Schisandra sphenanthera. J. Chromatogr. A. 2009, 1216, 1980-1990.
[2] Panossian, A.; Wikman, G. Pharmacology of Schisandra chinensis Bail.: an overview of Russian research and uses in medicine. J. Ethnopharmacol. 2008, 118, 183-212.
[3] Smejkal, K.; Slapetová, T.; Krmenčík, P.; Babula, P.; Dall‟Acqua, S.; Innocenti, G.; Vančo, J.; Casarin, E.; Carrara, M.; Kalvarová, K.; Dvorská, M.; Slanina, J.; Kramářová, E.; Julínek, O.; Urbanová, M. Evaluation of cytotoxic activity of Schisandra chinensis lignans. Planta Med. 2010, 76, 1672-1677.
[4] Chen, Y.C.; Liaw, C.C.; Cheng, Y.B.; Lin Y.C.; Chen, C.H.; Huang, Y.T.; Liou, S.S.; Chen, S.Y.; Chien, C.T.; Lee, G.C.; Shen, Y.C. Anti-liver fibrotic lignans from the fruits of Schisandra arisanensis and Schisandra sphenanthera. Bioorg. Med. Chem. Lett. 2013, 23, 880-885.
[5] Gao, X.; Meng X.J.; Li, J.H.; Tong H.B. Isolation, characterization and hypoglycemic activity of an acid polysaccharide isolated from Schisandra chinensis (turcz.) baill. Lett. Org. Chem. 2009, 6, 428-433.
[6] Huang, S.X.; Li, R.T.; Liu, J.P.; Lu,Y.; Chang, Y.; Lei, C.; Xiao,W.L.; Yang, L.B.; Zheng, Q.T.; Sun, H.D. Isolation and characterization of biogenetically related highly oxygenated nortriterpenoids from Schisandra chinensis. Org. Lett. 2007, 9, 2079-2082.
[7] Xue, Y.B.; Zhang, Y.L.; Yang, J.H.; Du, X.; Pu, J.X.; Zhao, W.; Li, X.N.; Xiao, W.L.; Sun, H.D. Nortriterpenoids and lignans from the fruit of Schisandra chinensis. Chem. Pharm. Bull. 2010, 58, 1606-1611.
[8] Huang, S.X.; Han, Q.B.; Lei, C.; Pu, J.X.; Xiao, W.L.; Yu, J.L.; Yang, L.M.; Xu, H.X.; Zheng, Y.T.; Sun, H.D. Isolation and characterization of miscellaneous terpenoids of Schisandra chinensis. Tetrahedron. 2008, 64, 4260-4267.
[9] Wang, H.J.; Chen, Y.Y. Studies of lignans from Schisandra rubriflora rhed et wils. Acta Pharm. Sin. 1985, 20, 832-841.
[10] Wang, X.Y.; Chen, G.R.; Deng, Z.Y.; Zhao, J.; Ge, J.F.; Li, N.; Chen, F.H. Chemical constituents from Bidens bipinnata. China J. Chin. Mater. Med. 2014, 39, 1838-1844.
[11] Hu, H.B.; Fan, J. A new acylated stilbene glycoside from Acanthopanax brachypus. Bull. Korean Chem. Soc. 2009, 30, 703-706.
[12] D‟Agostino, M.; de Feo, V.; de Simone, F.; Pizza, C. Three chalcones from Senecio pseudotites. Phytochemistry. 1991, 30, 2440-2441.
[13] Narui, T.K.; Sawada, K.; Takatsuki, S.; Okuyama, T.; Culberson, C.F.; Culberson, W.L.; Shibata, S. NMR assignments of depsides and tridepsides of the lichen family Umbilicariaceae. Phytochemistry. 1998, 48, 815-822.
[14] Zhang, X.N.; Bai, M.; Cheng, Z.Y.; Yu, Z.G.; Huang, X.X. Cytotoxic lignans from the barks of Juglans mandshurica. J. Asian. Nat. Prod. Res. 2018, 20, 494-499.
[15] Ramjith, U.S.; Ayda C.; Navneeth, K.M.; Sameer. P.A.; Smrithi, R. Molecular docking study of aspirin and aspirin derivatives. IOSR J. Appl. Chem. 2013, 3, 24-30. |