BENZOPHENONE GLUCOSIDE ISOLATED FROM THE ETHYL ACETATE EXTRACT OF THE BARK OF MAHKOTA DEWA [Phaleria macrocarpa (Scheff.) Boerl.] AND ITS INHIBITORY ACTIVITY ON LEUKEMIA L1210 CELL LINE

https://doi.org/10.22146/ijc.21576

Hendig Winarno(1*), Ermin Katrin W(2)

(1) Center for the Application of Isotopes and Radiation Technology, BATAN, Jakarta Jl. Cinere Pasar Jumat, Lebak Bulus, Jakarta 12440
(2) Center for the Application of Isotopes and Radiation Technology, BATAN, Jakarta Jl. Cinere Pasar Jumat, Lebak Bulus, Jakarta 12440
(*) Corresponding Author

Abstract


Isolation and elucidation of benzophenone glucoside from ethyl acetate extract of Phaleria macrocarpa bark and its inhibitory activity test against leukemia L1210 cell line have been done. The Phaleria macrocarpa bark were macerated using n-hexane, ethyl acetate, and ethanol, respectively. The ethyl acetate extract was then chromatographed on silica gel column and gradiently eluted by n-hexane - ethyl acetate - ethanol with the composition from 20:1:0 until 0:0:1, gave eight fractions. Separation of fraction 6 using semipreparative HPLC on reverse phase column (Capcell Pak C-18 SG120, 15 mm I.D. x 250 mm) using methanol - water (40:60, 5 mL/min) gave a brown powder, with the melting point of 182.3 ºC. Spectroscopic analysis and comparison of its physico-chemical data, this compound was clarified as 2,4'-dihydroxy-4-methoxy-benzophenone-6-O-b-D-glucopyranoside (3). Inhibitory activity of its compound against leukemia L1210 cell line showed that this compound exhibited inhibitory activity with IC50 was 5.1mg/mL.


Keywords


Phaleria macrocarpa; 2,4'-dihydroxy-4-methoxybenzophenone-6-O-b-D-glucopyranoside; cytotoxic activity; leukemia L1210

Full Text:

Full Text PDF


References

[1] Aditama, T.Y., Kanker, 2001, Medisinal Jurnal Kedokteran, 2, 1-5.

[2] Anonymous, Mahkota Dewa Nusantara (Phaleria macrocarpa (Scheff.) Boerl.). http://www.trubus-online.com, to be accessed on March 11, 2008.

[3] Wahyuningsih, M.S.H., Mubarika, S., Gandjar, I.G., Hamann, M.T., Rao, K.V., and Wahyuono, S., 2005, Indonesian J. Pharm., 16 (1), 51-57.

[4] Zhang, Y-B., Xu, X-J., and Liu, H-M., 2006, J. Asian Nat. Prod. Res., 8 (1-2), 119-123.

[5] Winarno, E.K. and Winarno, H., 2008, J. Traditional Medicine. Submitted.

[6] Silverstein, R.M., Bassler, G.C, and Morrill, T.C., 1991, Spectrometric Identification of Organic Compounds, 5th ed., John Wiley & Sons, Inc., New York.

[7] Ferrari, J., Terreaux, C., Sahpaz, S., Msonthi, J.D., Wolfender, J.L., and Hostettmann, K., 2000, Phytochemistry, 54 (8), 883-889.

[8] Kusmardiyani, S., Nawawi, A., Rahmi, K., 2004, Acta Pharmaceutica Indonesia, 29 (4), 150-152.

[9] Tambunan, R.M. and Simanjuntak, P., 2006, Indonesian J. Pharm., 17 (4), 184-189.

[10] Swanson, S.M. and Pezzuto, J.M., 1990, Bioscreening Tehnique for Cytotoxic Potential and Ability to Inhibit Macromolecule Biosynthesis, in: Drug Bioscreening, Thompson, E. B. Ed., John Wiley & Sons, New York, 273-297.



DOI: https://doi.org/10.22146/ijc.21576

Article Metrics

Abstract views : 2244 | views : 2585


Copyright (c) 2010 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.