Dammarane-type glycosides and long chain sesquiterpene glycosides from Gynostemma yixingense

Fitoterapia

Volumn 81, Issue 4, 2010, Pages 248-252

  Xiang, Wen Juan ^a   Guo, Chun Yu ^a   Ma, Lei ^a   Hu, Li Hong ^a,b  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Dammarane type glycoside; Gynostemma yixingense; Long chain sesquiterpene glycoside

Indexed keywords

(2E,63) 10 BETA DELTA GLUCOPYRANOSYL 1,10,11 TRIHYDROXY 3,7,11 TRIMETHYLDODECA 2,6 DIENE; 20 GINSENOSIDE RG2; 20 GINSENOSIDE RH1; 2ALPHA, 3BETA, 20 TRIHYDROXYDAMMAR 24 ENE 3 O [BETA DELTA GLUCOPYRANOSYL((1-2) BETA DELTA GLUCOPYRANOSYL)] 20 O [BETA DELTA XYLOPYRANOSYL((1-6) BETA DELTA GLUCOPYRANOSIDE)]; AMARANTHOLIDOSIDE; DAMMARANE DERIVATIVE; GINSENOSIDE F1; GINSENOSIDE RC; GINSENOSIDE RD; GLYCOSIDE; GYPENOSIDE XLVI; SAPONIN DERIVATIVE; SESQUITERPENE; UNCLASSIFIED DRUG; DAMMARANE; PLANT EXTRACT; TRITERPENE;

ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; CUCUMBER; DRUG ISOLATION; ELECTROSPRAY MASS SPECTROMETRY; GYNOSTEMMA YIXINGENSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; SPECTROSCOPY; STRUCTURE ANALYSIS; CHEMISTRY; GYNOSTEMMA; PLANT;

GLYCOSIDES; GYNOSTEMMA; MOLECULAR STRUCTURE; PLANT COMPONENTS, AERIAL; PLANT EXTRACTS; SESQUITERPENES; TRITERPENES;

GYNOSTEMMA;

EID: 77950521270     PISSN: 0367326X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fitote.2009.09.009     Document Type: Article

References (24)

1. Cui J.F., Eneroth P., and Bruhn J.G. Eur J Pharm Sci 8 (1999) 187
2. Attawish A., Chivapat S., Phadungpat S., Bansiddhi Y., Techadamrongsin J., Mitrijit O., Chaorai B., and Chavalittumrong P. Fitoterapia 75 (2004) 539
3. Lin C.C., Huang P.C., and Lin J.M. Am J Chin Med 28 1 (2000) 87
4. Zhang C., Yang X., and Xu L. Zhong Xi Yi Jie He Za Zhi 10 2 (1990) 69
5. Chiu T.H., Chen J.C., and Chung J.G. In Vivo 17 3 (2003) 281
6. Lewis D.A., and Hanson P.J. Prog. Med. Chem. 28 (1991) 201
7. Huang T.H.W., Razmovski-Naumovski V., Salam N.K., Duke R.K., Tran V.H., Duke C.C., and Roufogalis B.D. Biochem Pharmacol 70 9 (2005) 1298
8. Circosta C., De Pasquale R., and Occhiuto F. Phytomedicine 12 (2005) 638
9. Valentina R.N., Huang T.H.W., Tran V.H., Li G.Q., et al. Phytochem Rev 4 (2005) 197
10. Piacenta S., and Pizza C. J Nat Prod 58 (1995) 512
11. Yin F., Zhang Y.N., Yang Z.Y., et al. J Nat Prod 69 (2006) 1394
12. Yin F., and Hu L.H. Helv Chim Acta 88 (2005) 1126
13. Dou D.Q., Li W., Guo N., Fu R., et al. Chem Pharm Bull 54 (2006) 751
14. Fiorentino A., Greca M.D., Abrosca, et al. Tetrahedron 62 (2006) 8952
15. Wang X.Y., Wang D., Ma X.X., et al. Helv Chim Acta 91 (2008) 60
16. Liao P.Y., Wang D., Zhang Y.J., and Yang C.R. J Agric Food Chem 56 (2008) 1751
17. Ko S.R., Suzuki Y., Suzuki K., et al. Chem Pharm Bull 55 (2007) 1522
18. Liu X., Ye W.C., Hsaio H.W.W., et al. Zhongguo Yaoke Daxue Xuebao 34 (2003) 21
19. Yoshikawa K., Arihara M., Kuki K., et al. Yakugaku Zasshi 107 (1987) 361
20. Yin F., Hu L.H., and Pan R.X. Chem Pharm Bull 52 (2004) 1440
21. Morimura K.I., Gatayama A., Tsukimata R., et al. Phytochemistry 67 (2006) 2681
22. Miyase T., Ueno A., Takizawa N., et al. Chem Pharm Bull 35 (1987) 1109
23. Maxwell A., and Rampersad D. J Nat Prod 52 3 (1989) 614
24. Diaz J.G., Goedken V.L., and Herz W. Chem Pharm Bull 31 (1992) 597