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Chemical Constituents and Anti-Acetylcholinesterase Activities of Dolomiaea wardii

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Abstract:

The chemical composition of the ethyl acetate and n-butanol extracts of Dolomiaea wardii has been reported for the first time in the present study and eight compounds were isolated and identified as corymbolone(1), encelin(2), 8-oxoargentone(3), betulinic acid(4), lupeol(5), 4-hydroxyacetophenone(6), sweroside(7), Laganoside(8). anti-acetylcholinesterase activity of 1-8 showed that compound 6 have weak inhibitory activity with IC50 value of 1.43 mM.

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Periodical:

Advanced Materials Research (Volumes 634-638)

Pages:

901-904

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.634-638.901

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Online since:

January 2013

Authors:

Chun Lei Li, Jie Sheng

Keywords:

Acetylcholinesterase Inhibitory Activities, Chemical Constituents, Dolomiaea wardii

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© 2013 Trans Tech Publications Ltd. All Rights Reserved

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References

[1] Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Flora of Tibet, (Xining people's Publications , 1991), p.223.

Google Scholar

[2] G. L. Ellman, K. D. Courtney, V. Andres and R. M. Featherstone, Biochem. Pharm., Vol. 7 (1961), p.88.

Google Scholar

[3] I. Orhan, B. Sener, M. I. Choudhary and A. Khalid, J. Ethno. Vol. 91 (2004), p.57.

Google Scholar

[4] A. G Juan, G. Vicente and C. C. Maria, J. Nat. Prod., Vol. 48 (1985), p.323.

Google Scholar

[5] L. Zdero，F. Bohlmann and R. M. King, Phytochemistry, Vol. 29 (1990), p.3201.

Google Scholar

[6] G. T. Maatooq, D. K. Stumpf, J. J. Hoffmann, L. K. Hutter and B. N. Timmermann, Phytocheraistry, Vol. 41 (1996), p.519.

Google Scholar

[7] M. Sholichin, K. Yamasaki, R. Kasai and O. Tanaka, Chem. Pharm. Bull., Vol. 28 (1980), p.1006.

Google Scholar

[8] S. Furukawa, N. Takagi, T. Ikeda, M. Ono, A. M. Nafady, T. Nohara, H. Sugimot, S. Doi and H. Yamada, Chem. Pharm. Bull., Vol. 50 (2002), p.439.

DOI: 10.1248/cpb.50.439

Google Scholar

[9] X. J. Gong, H. Y. Zhu, X. S. Yang and X. J. Hao, Nat. Prod. Res. Dev., Vol. 18 (Suppl) (2006), p.50.

Google Scholar

[10] W. G. Ma，N. Fuzzati，J. L. Wolfender, K. Hostettmann and C. R. Yang, Helv. Chim. Acta, Vol. 77 (1994), p.1660.

DOI: 10.1002/hlca.19940770621

Google Scholar

[11] A. H. Heckendorf, K. C. Mattes and C. Hutchinson, J. Org. Chem., Vol. 41 (1976), p. (2045).

Google Scholar

[12] M. C. M. Young，M. R. Braga, S. M. C. Dietrich, H. E. Gottlieb, L. M. V. Trevisan and V. D. S. Bolzani, Phytochemistry, Vol. 31 (1992), p.3433.

DOI: 10.1016/0031-9422(92)83701-y

Google Scholar