Chemical composition and hepato-protective activity of Imperata cylindrica Beauv.

Pharmacognosy Magazine

Volumn 4, Issue 17, 2009, Pages 28-36

  Mohamed, Gamal A ^a   Abdel Lateff, Ahmed ^b   Fouad, Mostafa A ^b   Ibrahim, Sabrin R M ^c   Elkhayat, Ehab S ^a   Okino, Tatsufumi ^d  

^a Al Azhar University   (Egypt)

^b Minia University   (Egypt)

^c Assiut University   (Egypt)

^d HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Hepato protective activity; Imperata cylindrica; Methoxylated flavonoids; Steroids

Indexed keywords

3 HYDROXY 4 METHOXYBENZALDEHYDE; 3,5 DI O METHYLKAEMPFEROL; ALPHA AMYRIN; BETA SITOSTEROL 3 O BETA DEXTRO GLUCOPYRANOSYL 6' TETRADECANOATE; DAUCOSTEROL; FLAVONOID; IMPERATA CYLINDRICA EXTRACT; JACEIDIN; PLANT EXTRACT; QUERCETAGETIN 3,5,6,3' TETRAMETHYL ETHER; SITOSTEROL; TRICIN; UNCLASSIFIED DRUG; METHANOL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CHEMICAL COMPOSITION; CONTROLLED STUDY; DRUG DETERMINATION; DRUG IDENTIFICATION; DRUG STRUCTURE; IMPERATA CYLINDRICA; LIVER PROTECTION; LIVER TOXICITY; MALE; NONHUMAN; PHYTOCHEMISTRY; POACEAE; RAT; STRUCTURE ANALYSIS; DRUG EFFECT; DRUG EFFICACY; DRUG ISOLATION;

EID: 74049134010     PISSN: 09731296     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (29)

1. J. H.Park, Medicinal plants of Korea, (Shinil Publishing Co., Seoul, 2004), p. 101.
2. J. S. Yoon, M. K. Lee, S. H. Sung, Y. C. Kim. Neuroprotective 2-(2-Phenylethyl)chromones of Imperata cylindrica. J. Nat. Prod. 69: 290-291 (2006).
3. K. Nishimoto, M. Ito, S. Natori, T. Ohmoto. The structures of arundoin, cylindrin and fernenol: Triterpenoids of fernane and arborane groups of Imperata cylindrica var. koenigii. Tetrahedron, 24: 735-752 (1968).
4. K. Matsunaga, M. Ikeda, M. Shibuya, Y. Ohizuni. Cylindol A, a Novel Biphenyl Ether with 5-Lipoxygenase Inhibitory Activity, and a Related Compound from Imperata cylindrica. J. Nat. Prod., 57: 1290-1293 (1994).
5. K. Matsunaga, M. Shibuya, Y. Ohizuni. Cylindrene, a Novel Sesquiterpenoid from Imperata clylindrica with Inhibitory Activity on Contractions of Vascular Smooth Muscle. J. Nat. Prod., 57: 1183-1184 (1994).
6. M. Matsunaga, M. Shibuya, Y. Ohizuni. Graminone B, a Novel Lignan with Vasodilative Activity from Imperata cylindrica. J. Nat. Prod., 57: 1734-1736 (1994).
7. M. Matsunaga, M. Shibuya, Y. Ohizuni. Imperanene, a Novel Phenolic Compound with Platelet Aggregation Inhibitory Activity from Imperata cylindrica. J. Nat. Prod., 58: 138-139 (1995).
8. K. Nakano, K. Murakami, T. Nohara, T. Tomimastu, T. Kawasaki. The Constituents of Paris verticillata M.V. BIEB. Chem. Pharm. Bull., 29: 1445-1451 (1981).
9. P. K. Agrawal, Carbon-13 NMR of Flavonoids, (Elsevier Science B. V. Amsterdam, Oxford, New York, Tokyo 1989).
10. J. N. Roitman, L.F. James. Chemistry of toxic range plants. Highly oxygenated flavonol methyl ethers from Gutierrezia microcephala. Phytochemistry, 24: 835-848 (1985).
11. L. E. Urbatsch, J. D. Bacon, T. J. Mabry, D. M. Smith. Flavonol methyl ethers from Chrysothamnus viscidiflorus. Phytochemistry, 14: 2279-2282 (1975).
12. R. Kapoor, A. K. Rishi, C. K. Atal. a Rareyl Methylated New Flavonol Aglycone from Linaria dalmatica. Fitoterapia, 56: 296-297 (1985).
13. A. G. Ramachandran, P. Ramesh, S. S. Subramanian, B. S. Joshi. Rare methylated flavonols from Angelonia grandiflora. Phytochemistry, 17: 591-592 (1978).
14. L. E. Urbatsch, T. J. Mabry, M. Miyakodo, N. Ohno, H. Yoshioka. Flavonol methyl ethers from Ericameria diffusa. Phytochemistry, 15: 440-441 (1976).
15. K. R. Markham, T. J. Mabry, The Flavonoids, (J. B. Harbon, T. J. Mabry and H. Mabry; Academic Press: New York, 1975).
16. G. M. Woldemichael, S. G. Franzblau, F. Zhang, Y. Wang, B. N. Timmermann. Inhibitory Effect of Sterols from Ruprechtia triflora and Diterpenes from Calceolaria pinnifolia on the Growth of Mycobacterium tuberculosis. Planta Med., 69: 628-631 (2003).
17. C. J. Pouchert, Aldrich Library of NMR Spectra, (First Edition, 2, 1983) p.118 B.
18. B. N. Mayer, N. R. Ferrigni, J. E. Putnam, L. B. Jacobsen, D. E. Nichols, J. L. McLaughlin. A convenient General Bioassay for Active Plant Constituents. Planta Med., 45: 31-34 (1982).
19. R. Edrada, P. Proksch, V. Wray, L. Witte, L. Ofwegen. Four New Bioactive Lobane Diterpenes of the Soft Coral Lobophytum pauciflorum from Mindoro, Philippines. J. Nat. Prod., 61: 358 -361(1998).
20. A. Bosma. Synergism between ethanol and carbon tetrachloride in the generation of liver fibrosis. Journal of Pathology, 156: 15- (1988).
21. H.U. Bergmeyer, E.Bernt, Methods of Enzymatic Analysis, (Vol. 2, 2nd Ed. New York, Academic Press 1974), p.735.
22. T. J. Mabry, K. R. Markham, M. B. Thomas, The Systematic Identification of Flavonoids, (Springer Verlage, New York, Heidelberg, Berlin 1970), p. 260-273.
23. J. B. Harborne, The Flavonoids Advances in Research Since 1986, (Chapman and Hall, London 1994), p. 480.
24. J. Sakakibara, T. Kaiya, H. Fukuda, T. Ohki. 6-β-Hydroxyursolic acid and other triterpenoids of Enkianthus cernuus. Phytochemistry, 22: 2553-2555 (1983).
25. P. K. Agrawal. NMR Spectroscopy in the structural elucidation of oligosaccharides and glycosides. Phytochemistry, 31: 3307-3330 (1992).
26. 13C NMR assignments of stigma-5-en-3-Ο-b-glucoside and its acetyl derivative. Magn. Reson. Chem., 39: 399 (2001).
27. X. Yuan, B. Li, X. Zhang, H. Qi, M. Zhou, G. Zhang. Two Diterpenes and Three Diterpene Glucosides from Phlogacanthus curviflorus. J. Nat. Prod., 68 (1): 86-89 (2005).
28. T. Mills, J. C. Robertson, Instrumental Data for Drug Analysis, (Elsevier Publishing, New York, Amesterdam, London 1987) p. 2094.
29. M. Lima, P. de Campos Braga, M. Macedo, M. Fátima, G. da Silva, A. Ferreira, J. Fernandes, P. Vieira. Phytochemistry of Trattinnickia burserifolia, T. rhoifolia, and Dacryodes hopkinsii: chemosystematic implications. J. Braz. Chem. Soc. 15 (3): 385-394 (2004).