Two new steroidal saponins from Tribulus terrestris

Journal of Asian Natural Products Research

Volumn 11, Issue 1, 2009, Pages 38-43

  Su, Lan ^a   Feng, Sheng Guang ^a   Qiao, Li ^a   Zhou, Yu Zhi ^a   Yang, Rui Ping ^a   Pei, Yue Hu ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

Flavonoid glycosides; Steroidal saponins; Tribulus terrestris

Indexed keywords

26 O BETA DEXTRO GLUCOPYRANOSYL 5ALPHA FUROSTAN 12 ONE 3BETA,22ALPHA,26 TRIOL 3 O BETA DEXTRO GLUCOPYRANOSYL (1-2) BETA DEXTRO GLUCOPYRANOSYL (1-4) BETA DEXTRO GALACTOPYRANOSIDE; 26 O BETA DEXTRO GLUCOPYRANOSYL 5ALPHA FUROSTAN 22 METHOXY 2ALPHA,3BETA,26 TRIOL 3 O BETA DEXTRO GLUCOPYRANOSYL (1-2) BETA DEXTRO GLUCOPYRANOSYL (1-4) BETA DEXTRO GALACTOPYRANOSIDE; FLAVONOID GLYCOSIDE; ISORHAMNETIN 3 GENTIOBIOSIDE; KAEMPFEROL 3 GENTIOBIOSIDE; SAPONIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ISOLATION; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; FRUIT; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; NONHUMAN; PHYTOCHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; THIN LAYER CHROMATOGRAPHY; TRIBULUS TERRESTRIS;

DRUGS, CHINESE HERBAL; FLAVONOIDS; FRUIT; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHYTOSTEROLS; SAPONINS; STEREOISOMERISM; TRIBULUS;

TRIBULUS TERRESTRIS;

EID: 60749134461     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020802413130     Document Type: Article

References (19)

1. I. Kostova and D. Dinchev, Phytochem. Rev. 4, 111 (2005).
2. J.L. Li and S.S. Yang, Chin. Arch. Trad. Chin. Med. 24, 1509 (2006).
3. E. Bedir, I.A. Khan, and L.A. Walker, Pharmazie 57, 491 (2002).
4. Z. Tu, L.B. Ma, X.L. Li, D.G. An, W.J. Sun, Z.W. Guo, and J. Gao, Chem. J. Chin. Univ. 23, 600 (2002).
5. D. Dinchev, B. Janda, L. Evstatieva, W. Oleszek, M.R. Aslani, and I. Kostova, Phytochemistry 69, 176 (2007).
6. S.J. Zhang, W.J. Qu, and S.Y. Zhou, J. Chin. Mater. Med. 31, 910 (2006).
7. L.B. Li, J. Li, H. Li, S.J. Yang, and J. Harbin, Med. Univ. 40, 99 (2006).
8. V.K. Neychev, E. Nikolova, N. Zhelev, and V.I. Mitev, Exp. Biol. Med. 232, 126 (2007).
9. Q. Shi, B.Y. Yu, L.S. Xu, and G.J. Xu, Chin. J. Pharm. Anal. 19, 75 (1999).
10. Y. Wang, K. Ohtani, R. Kasai, and K. Yamasaki, Phytochemistry 45, 811 (1997).
11. P.K. Agrawal, Magn. Reson. Chem. 42, 990 (2004).
12. G. Wu, S.H. Jiang, F.X. Jiang, D.Y. Zhu, H.M. Wu, and S.K. Jiang, Phytochemistry 42, 1677 (1996).
13. L.F. Cai, F.Y. Jing, J.G. Zhang, F.K. Pei, Y.J. Xu, S.Y. Liu, and D.M. Xu, Acta Pharm. Sin. 34, 759 (1999).
14. Y. Zhang, H.Z. Li, Y.J. Zhang, M.R. Jacob, S.I. Khan, X.C. Li, and C.R. Yang, Steroids 71, 712 (2006).
15. S. Yahara, T. Ura, C. Sakamoto, and T. Nohara, Phytochemistry 37, 831 (1994).
16. H.M. Ho, R.Y. Chen, L.K. Leung, F.L. Chan, Y. Huang, and Z.Y. Chen, Biomed. Pharmacother. 56, 289 (2002).
17. N.A.M. Saleh, A.A. Ahmed, and M.F. Abdalla, Phytochemistry 21, 1995 (1982).
18. T.J. Hsich, Y.C. Wu, W.L. Lo, S.C. Chen, S.H. Kuo, and C.Y. Chen, Chin. Pharm. J. (Taipei, Taiwan) 56, 17 (2004).
19. H. Liang, Y.Y. Zhao, Y.J. Cui, Q.X. Liu, and J. Beijing, Med. Univ. 32, 223 (2000).