Six new lignans from the leaves and stems of Schisandra sphenanthera

Fitoterapia

Volumn 86, Issue 1, 2013, Pages 171-177

  Liang, Cheng Qin ^a,c,d   Hu, Jing ^a   Luo, Rong Hua ^b,d   Shi, Yi Ming ^a,d   Shang, Shan Zhai ^a,d   Gao, Zhong Hua ^a,d   Wang, Rui Rui ^b   Zheng, Yong Tang ^b   Xiong, Wen Yong ^a   Zhang, Hong Bin ^c   Xiao, Wei Lie ^a   Sun, Han Dong ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b KUNMING INSTITUTE OF ZOOLOGY   (China)

^c YUNNAN UNIVERSITY   (China)

^d UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Anti HIV 1; Insulin sensitivity; Lignan; Schisandra sphenanthera; Schisandraceae

Indexed keywords

ANTIVIRUS AGENT; H SCHISPHENLIGNAN I; LIGNAN DERIVATIVE; PLANT EXTRACT; SCHISPHENLIGNAN F; SCHISPHENLIGNAN G; SCHISPHENLIGNAN H; SCHISPHENLIGNAN J; UNCLASSIFIED DRUG;

ADIPOCYTE; ANTIVIRAL ACTIVITY; ARTICLE; CIRCULAR DICHROISM; HUMAN IMMUNODEFICIENCY VIRUS 1; INSULIN RESISTANCE; INSULIN SENSITIVITY; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLANT LEAF; PLANT STEM; PRIORITY JOURNAL; SCHISANDRA; SCHISANDRA SPHENANTHERA;

3T3-L1 CELLS; ADIPOCYTES; ANIMALS; HIV-1; LIGNANS; MICE; MOLECULAR STRUCTURE; PLANT EXTRACTS; PLANT LEAVES; PLANT STEMS; SCHISANDRA;

HUMAN IMMUNODEFICIENCY VIRUS 1; SCHISANDRA SPHENANTHERA; SCHISANDRACEAE;

EID: 84876369394     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2013.03.008     Document Type: Article

References (39)

1. Y.H. Kuo, S.Y. Li, R.L. Huang, M.D. Wu, H.C. Huang, and K.H. Lee Schizarin B, C, D, and E, four new lignans from Kadsura matsudai and their antihepatitis activities J Nat Prod 64 2001 487 490
2. D.F. Chen, S.X. Zhang, K. Chen, B.N. Zhou, P. Wang, and L.M. Cosentino Two new lignans, interiotherins A and B, as anti-HIV principles from Kadsura interior J Nat Prod 59 1996 1066 1068
3. D.F. Chen, S.X. Zhang, M. Kozuka, Q.Z. Sun, J. Feng, and Q. Wang Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation J Nat Prod 65 2002 1242 1245
4. J.B. Chang, J. Reiner, and J.X. Xie Progress on the chemistry of dibenzocyclooctadiene lignans Chem Rev 105 2005 4581 4609
5. D.Y. Kwon, D.S. Kim, H.J. Yang, and S. Park The lignan-rich fractions of Fructus Schisandrae improve insulin sensitivity via the PPAR-γ pathways in in vitro and in vivo studies J Ethnopharmacol 135 2011 455 462
6. W.Z. Song, and P.G. Xiao The medical plants and lignans of Schisandraceae in China Chin Tradit Herb Drugs 13 1982 40 43
7. L. Opletal, H. Sovova, and M. Bartlova Dibenzo[a, c]cyclooctadiene lignans of the genus Schisandra: importance, isolation and determination J Chromatogr B 812 2004 357 371
8. W. Gu, N.Y. Wei, and Z.Z. Wang LC analysis of lignans from Schisandra sphenanthera Rehd. et Wils Chromatographia 67 2008 979 983
9. F. He, X.Y. Li, G.Y. Yang, X.N. Li, X. Luo, and J. Zou Nortriterpene constituents from Schisandra sphenanthera Tetrahedron 68 2012 440 446
10. F. He, J.X. Pu, S.X. Huang, Y.Y. Wang, W.L. Xiao, and L.M. Li Schinalactone A, a new cytotoxic triterpenoid from Schisandra sphenanthera Org Lett 12 2010 1208 1211
11. C.Q. Liang, J. Hu, Y.M. Shi, S.Z. Shang, X. Du, and R. Zhan Schisphenlignans A-E: five new dibenzocyclooctadiene lignans from Schisandra sphenanthera Chem Pharm Bull 61 2013 96 100
12. W.Y. Xiong, I. Jordens, E. Gonzalez, and T.E. McGraw GLUT4 is sorted to vesicles whose accumulation beneath and insertion into the plasma membrane are differentially regulated by insulin and selectively affected by insulin resistance Mol Biol Cell 21 2010 1375 1386
13. C.N.V. Prasad, T. Anjana, A. Banerji, and A. Gopalakrishnapillai Gallic acid induces GLUT4 translocation and glucose uptake activity in 3T3-L1 cells FEBS Lett 584 2010 531 536
14. M.J. Tan, J.M. Ye, N. Turner, C. Hohnen-Behrens, C.Q. Ke, and C.P. Tang Antidiabetic activities of triterpenoids isolated from bitter melon associated with activation of the AMPK pathway Chem Biol 15 2008 263 273
15. R.R. Wang, L.M. Yang, Y.H. Wang, W. Pang, S.C. Tam, and P. Tien Sifuvirtide, a potent HIV fusion inhibitor peptide Biochem Biophys Res Commun 382 2009 540 544
16. X.N. Li, J.X. Pu, X. Du, L.M. Yang, H.M. An, and C. Lei Lignans with anti-HIV activity from Schisandra propinqua var. sinensis J Nat Prod 72 2009 1133 1141
17. J. Kubanek, W. Fenical, M.E. Hay, P.J. Brown, and N. Lindquist Two antifeedant lignans from the freshwater macrophyte Saururus cernuus Phytochemistry 54 2000 281 287
18. R.C.C. Martins, L.R. Latorre, P. Sartorelli, and M.J. Kato Phenylpropanoids and tetrahydrofuran lignans from Piper solmsianum Phytochemistry 55 2000 843 846
19. A.A. da Silva, S. Albuquerque, M.L.A.E. Silva, M.N. Eberlin, D.M. Tomazela, and J.K. Bastos Tetrahydrofuran lignans from Nectandra megapotamica with trypanocidal activity J Nat Prod 67 2004 42 45
20. J.X. Pu, X.M. Gao, C. Lei, W.L. Xiao, R.R. Wang, and L.B. Yang Three new compounds from Kadsura longipedunculata Chem Pharm Bull 56 2008 1143 1146
21. M. Schottner, J. Reiner, and F.S.K. Tayman (+)-Neo-olivil from roots of Urtica dioica Phytochemistry 46 1997 1107 1109
22. Y.R. Li, W. Cheng, C.G. Zhu, C.S. Yao, L. Xiong, and Y. Tian Bioactive neolignans and lignans from the bark of Machilus robusta J Nat Prod 74 2011 1444 1452
23. M. Kikuchi, and M. Kikuchi Studies on the constituents of Swertia japonica MAKINO II. On the structures of new glycosides Chem Pharm Bull 53 2005 48 51
24. K.H. Kim, S.K. Ha, S.Y. Kim, H.J. Youn, and K.R. Lee Constituents of Limonia acidissima inhibit LPS-induced nitric oxide production in BV-2 microglia J Enzyme Inhib Med Chem 25 2010 887 892
25. A.K. Chakravarty, S. Mukhopadhyay, S. Saha, and S.C. Pakrashi A neolignan and sterols in fruits of Solanum sisymbrifolium Phytochemistry 41 1996 935 939
26. S. Valcic, G. Montenegro, and B.N. Timmermann Lignans from Chilean propolis J Nat Prod 61 1998 771 775
27. M.S.M. Yuen, F. Xue, T.C.W. Mak, and H.N.C. Wong On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton Tetrahedron 54 1998 12429 12444
28. A.A. El Gamal, K. Takeya, H. Itokawa, A.F. Halim, M.M. Amer, and H.E.A. Saad Lignan bis-glucosides from Galium sinaicum Phytochemistry 45 1997 597 600
29. W.J. He, Z.H. Fu, H.J. Han, H. Yan, G.Z. Zeng, and C.J. Ji Benzoic acid allopyranosides and lignan glycosides from the twigs of Keteleeria evelyniana Z Naturforsch B 66 2011 733 739
30. Q. Wu, D.X. Fu, A.J. Hou, G.Q. Lei, Z.J. Llu, and J.K. Chen Antioxidative phenols and phenolic glycosides from Curculigo orchioides Chem Pharm Bull 53 2005 1065 1067
31. T. Miyase, A. Ueno, N. Takizawa, H. Kobayashi, and H. Oguchi Studies on the glycosides of Epimedium grandiflorum MORR. var. thunbergianum (MIQ.) NAKAI. II Chem Pharm Bull 35 1987 3713 3719
32. S.K. Sadhu, E. Okuyama, H. Fujimoto, M. Ishibashi, and E. Yesilada Prostaglandin inhibitory and antioxidant components of Cistus laurifolius, a Turkish medicinal plant J Ethnopharmacol 108 2006 371 378
33. X.C. Chen, and Z.J. Jia Two new glycosides from Rubus amabilis Chin Chem Lett 11 2000 897 900
34. S.K. Sadhu, A. Khatun, P. Phattanawasin, T. Ohtsuki, and M. Ishibashi Lignan glycosides and flavonoids from Saraca asoca with antioxidant activity J Nat Med 61 2007 480 482
35. M. Shoeb, M.M. Rahman, L. Nahar, M. Jaspars, S. Macmanus, and A. Delazar Bioactive lignans from the seeds of Centaurea macrocephala DARU-J Tehran Sch Pharm 12 2004 87 93
36. Y. Ikeya, H. Taguchi, I. Yosioka, and H. Kobayashi Constituents of Schizandra chinensis Baill. I. Isolation and structure determination of five new lignans, gomisin A, B, C, F and G and the absolute structure of schizandrin Chem Pharm Bull 27 1979 1383 1394
37. H. Taguchi, and Y. Ikeya Constituents of Schizandra chinensis Baill. I. The structures of gomisin A, B and C Chem Pharm Bull 23 1975 3296 3298
38. M. Chen, N. Kilgore, K.H. Lee, and D.F. Chen Rubrisandrins A and B, lignans and related anti-HIV compounds from Schisandra rubriflora J Nat Prod 69 2006 1697 1701
39. A.M. Warshawsky, and A.I. Meyers Asymmetric total synthesis of dibenzocyclooctadiene lignans (-)-schizandrin and (-)-isoschizandrin. Structure revision of (+)-isoschizandrin J Am Chem Soc 112 1990 8090 8099