A new flavonol glycoside and activity of compounds from the flower of Nymphaea candida

Journal of Asian Natural Products Research

Volumn 9, Issue 4, 2007, Pages 333-338

  Liu, R N ^a   Wang, W ^a   Ding, Y ^a   Xie, W D ^a   Ma, C ^a   Du, L J ^a  

^a TSINGHUA UNIVERSITY   (China)

Author keywords

Antioxidation; Cytotoxicity; Flavonoid; Kaempferol 3 O (2 O galloylrutinoside); Neuroprotection; Nymphaea candida

Indexed keywords

FLAVANOL DERIVATIVE; GLYCOSIDE; KAEMPFEROL 3 O (2'' O GALLOYLRUTINOSIDE); KAEMPFEROL 3 O ALPHA LEVO RHAMNOPYRANOSIDE; KAEMPFEROL 3 O ALPHA LEVO RHAMNOPYRANOSYLGLUCOPYRANOSIDE; KAEMPFEROL 3 O BETA DEXTRO GLUCOPYRANOSIDE; KAEMPFEROL 7 O BETA DEXTRO GLUCOPYRANOSIDE 3 (O ALPHA LEVO RHAMNOPYRANOSYLGLUCOPYRANOSIDE); LOW DENSITY LIPOPROTEIN; MALONALDEHYDE; MYRICETIN; MYRICETIN 3' BETA DEXTRO XYLOPYRANOSIDE; QUERCETIN; QUERCETIN 3 O BETA DEXTRO XYLOPYRANOSIDE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANTIOXIDANT ACTIVITY; ARTICLE; BRAIN ISCHEMIA; CONTROLLED STUDY; CULTURE MEDIUM; CYTOTOXICITY; DRUG ACTIVITY; DRUG ISOLATION; DRUG STRUCTURE; FLOWER; IN VITRO STUDY; NEUROPROTECTION; NEWBORN; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NYMPHAEA; NYMPHAEA CANDIDA; PHEOCHROMOCYTOMA CELL; RAT;

ANIMALS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; ANTIOXIDANTS; DISACCHARIDES; FLAVONOLS; FLOWERS; GLYCOSIDES; KAEMPFEROLS; MAGNETIC RESONANCE SPECTROSCOPY; NEUROPROTECTIVE AGENTS; NYMPHAEA; PC12 CELLS; RATS;

NYMPHAEA CANDIDA; RATTUS;

EID: 34447126901     PISSN: 10286020     EISSN: 14772213     Source Type: Journal    
DOI: 10.1080/10286020600727665     Document Type: Article

References (15)

1. X.M. Ni, B. Yu, Y.J. Zhou, J.R. Zhao. J. Wuhan. Botan. Res., 13, 137 (1995).
2. P. Sheng, D.M. Zhang. Chin. J. Ethnomed. Ethnopharm., 12, 302 (2003).
3. B. Gerd, J Birgitta. Phytochemistry, 10, 471 (1971).
4. H. Bukowiecki, M. Furmanowa. Acta. Polon. Pharm., 21, 121 (1964).
5. T. Fossen, A. Larsen. Phytochemistry, 48, 823 (1998).
6. T. Fossen, N.A. Froystein, O.M. Andersen. Phytochemistry, 49, 1997 (1998).
7. T.A. Byung, J.O. Kap, S.R. Jai, S.L. Kyong. Planta Med., 62, 383 (1996).
8. B. Li, Y.M. Luo. Jiangxi College of Traditional Chinese Med., Nanchang, Peop. Rep. Chin. Chem. J. Inter., 5 No pp. given (2003).
9. T. Fossen, O.M. Andersen. Phytochemistry, 50, 1195 (1999).
10. S. Beckmann, H. Geiger. Phytochemistry, 2, 281 (1963).
11. K.R. Markham, E.S. Viotto. Phytochemistry, 27, 307 (1988).
12. Y. Tian, J. Wu, S.J. Zhang. Chin. Pharm. Sci., 13, 214 (2004).
13. S. Varathan, S. Shibuta, T. Shimizu, T.J. Mashimo. Neurosci. Res., 65, 583 (2001).
14. J.F. Wu, S.L. Liu, X.X. Pan, T.P. Liu. Chin. Pharm. Bull., 15, 243 (1999).
15. R.F. Wang, W.D. Xie, Zh. Zhang, D.M. Xing, Y. Ding, W. Wang, Ch. Ma, L.J. Du. J. Nat. Prod., 67, 2096 (2004).