Sesquiterpenoids and further diterpenoids from the rare Chloranthaceae plant Chloranthus sessilifolius

Journal of Asian Natural Products Research

Volumn 17, Issue 12, 2015, Pages 1220-1230

  Wang, Li Jun ^a   Xiong, Juan ^a   Lau, Choiwan ^a   Pan, Li Long ^a   Hu, Jin Feng ^a  

^a FUDAN UNIVERSITY   (China)

Author keywords

antineuroinflammation; Chloranthaceae; Chloranthus sessilifolius; diterpenoids; sesquiterpenoids

Indexed keywords

3 HYDROXY ENT PODOCARPA 8(14) ENE 13 ONE; 3 HYDROXYATRACTYLENOLIDE III; 3ALPHA HYDROXY ENT TORARA 8 EN 7,13 DIONE; 3ALPHA,7BETA DIHYDROXY ENT ABIETA 8,11,13 TRIENE; ANTIINFLAMMATORY AGENT; CHLORAJAPOLIDE D; CHLORASESSILIFOL A; CHLORASESSILIFOL B; CYCLOSHIZUKAOL A; DECANDRIN B; DECANDRIN G; DITERPENOID; LASIANTHUSLACTONE A; LIPOPOLYSACCHARIDE; N(G) METHYLARGININE; NITRIC OXIDE; SESQUITERPENOID; UNCLASSIFIED DRUG; 3ALPHA,7BETA-DIHYDROXY-ENT-ABIETA-8,11,13-TRIENE; ABIETANE DERIVATIVE; DITERPENE; HERBACEOUS AGENT; NONSTEROID ANTIINFLAMMATORY AGENT; SESQUITERPENE;

ANIMAL CELL; ANTIINFLAMMATORY ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CELL VIABILITY; CHLORANTHUS SESSILIFOLIUS; CIRCULAR DICHROISM; CONTROLLED STUDY; HETERONUCLEAR MULTIPLE BOND CORRELATION; MEDICINAL PLANT; MOUSE; NONHUMAN; NUCLEAR OVERHAUSER EFFECT; PHYSICAL CHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; ANGIOSPERM; ANIMAL; BIOSYNTHESIS; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; IC50; ISOLATION AND PURIFICATION; MACROPHAGE; MICROGLIA; NUCLEAR MAGNETIC RESONANCE;

ANGIOSPERMS; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; DITERPENES; DITERPENES, ABIETANE; DRUGS, CHINESE HERBAL; INHIBITORY CONCENTRATION 50; LIPOPOLYSACCHARIDES; MACROPHAGES; MICE; MICROGLIA; MOLECULAR STRUCTURE; NITRIC OXIDE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; SESQUITERPENES;

EID: 84955204571     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020.2015.1118622     Document Type: Article

References (25)

1. A.R. Wang, H.C. Song, H.M. An, Q. Huang, X. Luo, and, J.Y. Dong., Chem. Biodivers. 12, 451 (2015). 10.1002/cbdv.201300376
2. L.J. Wang, J. Xiong, S.T. Liu, X.H. Liu, and, J.F. Hu., Chem. Biodivers. 11, 919 (2014). 10.1002/cbdv.v11.6
3. S.T. Liu, J. Xiong, Y. Tang, W.X. Wang, V.B. Bui, G.L. Ma, Y. Huang, Y. Zhao, G.X. Yang, and, J.F. Hu., Chem. Biodivers. 11, 904 (2014). 10.1002/cbdv.v11.6
4. J. Xiong, S.T. Liu, Y. Tang, W.X. Wang, V.B. Bui, Y. Zhao, H. Fan, G.X. Yang, and, J.F. Hu., Phytochem. Lett. 6, 586 (2013). 10.1016/j.phytol.2013.07.015
5. Y.Q. Chen, D.Z. Cheng, G.F. Wu, P.S. Cheng, and, P.Z. Zhu, (eds.): Editorial Committee of Flora Republicate Popularis Sinicae., in Chinese Flora (Science Press, Beijing, 1982), Vol. 20, pp 80-96.
6. D.Q. Wang., Lishizhen Med. Mater. Med. Res. 2, 140 (1991).
7. L.J. Wang, J. Xiong, S.T. Liu, L.L. Pan, G.X. Yang, and, J.F. Hu., J. Nat. Prod. 78, 1635 (2015). 10.1021/acs.jnatprod.5b00195
8. J. Xiong, V.B. Bui, X.H. Liu, Z.L. Hong, G.X. Yang, and, J.F. Hu., J. Ethnopharmacol. 153, 737 (2014). 10.1016/j.jep.2014.03.036
9. J. Xiong, X.H. Liu, V.B. Bui, Z.L. Hong, L.J. Wang, Y. Zhao, H. Fan, G.X. Yang, and, J.F. Hu., Fitoterapia. 94, 114 (2014). 10.1016/j.fitote.2014.02.002
10. S.Y. Kim, Y. Kashiwada, K. Kawazoe, K. Kawazoe, K. Murakami, H.D. Sun, S.L. Li, and, Y. Takaishi., Chem. Pharm. Bull. 59, 1281 (2011). 10.1248/cpb.59.1281
11. S.P. Yang, Z.B. Gao, F.D. Wang, S.G. Liao, H.D. Chen, C.R. Zhang, G.Y. Hu, and, J.M. Yue., Org. Lett. 9, 903 (2007). 10.1021/ol0700759
12. X.H. Ran, F. Teng, C.X. Chen, G. Wei, X.J. Hao, and, H.Y. Liu., J. Nat. Prod. 73, 972 (2010). 10.1021/np900764n
13. S.Y. Kim, Y. Kashiwada, K. Kawazoe, K. Murakami, H.D. Sun, S.L. Li, and, Y. Takaishi., Phytochem. Lett. 2, 110 (2009). 10.1016/j.phytol.2009.03.001
14. S.P. Yang, Z.B. Gao, Y. Wu, G.Y. Hu, and, J.M. Yue., Tetrahedron. 64, 2027 (2008). 10.1016/j.tet.2007.12.057
15. J.Y. Li, Y. Peng, L.Z. Li, P.Y. Gao, C. Gao, S.X. Xia, and, S.J. Song., Helv. Chim. Acta. 96, 313 (2013). 10.1002/hlca.v96.2
16. G.D. Prestwich, and, J.N. Labovitz., J. Am. Chem. Soc. 96, 7103 (1974). 10.1021/ja00829a050
17. E.M. Addo, H.-B. Chai, A. Hymete, M.Y. Yeshak, C. Slebodnick, D.G.I. Kingston, and, L.H. Rakotondraibe., J. Nat. Prod. 78, 827 (2015). 10.1021/np501062f
18. S. Itô, and, M. Kodama., Heterocycles. 4, 595 (1976). 10.3987/R-1976-03-0595
19. J. Kawabata, E. Fukushi, and, J. Mizutani., Phytochemistry. 32, 1347 (1993). 10.1016/S0031-9422(00)95119-7
20. Q.H. Wang, H.X. Kuang, B.Y. Yang, Y.G. Xia, J.S. Wang, and, L.Y. Kong., J. Nat. Prod. 74, 16 (2011). 10.1021/np100504m
21. B. Li, D.M. Zhang, and, Y.M. Luo., Acta Pharm. Sin. 41, 426 (2006).
22. Y.J. Xu, C.P. Tang, M.J. Tan, C.Q. Ke, T. Wu, and, Y. Ye., Chem. Biodivers. 7, 151 (2010). 10.1002/cbdv.v7:1
23. H. Wang, M.Y. Li, T. Satyanandamurty, and, J. Wu., Planta Med. 79, 666 (2013).
24. C.M.A. Tanaka, V.S.C.O. Radke, C.C. Silva, C.V. Nakamura, P.L. Oliveira, L. Kato, and, C.M.A. Oliveira., Quim. Nova. 33, 30 (2010). 10.1590/S0100-40422010000100006
25. X.D. Tian, Z.D. Min, N. Xie, Y. Lei, Z.Y. Tian, Q.T. Zheng, R.N. Xu, T. Tanaka, M. Iinuma, and, M. Mizuno., Chem. Pharm. Bull. 41, 1415 (1993). 10.1248/cpb.41.1415