MACRONONE, A NOVEL DIEPOXYLIGNAN FROM BARK OF MAHKOTA DEWA (Phaleria macrocarpa (Scheff.) Boerl.) AND ITS ANTIOXIDANT ACTIVITY

https://doi.org/10.22146/ijc.21373

Susilawati Susilawati(1*), Sabirin Matsjeh(2), Harno Dwi Pranowo(3), Chairil Anwar(4)

(1) Department of Education of Mathematics and Natural Sciences, FKIP, Universitas Riau, Pekanbaru
(2) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281
(3) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281
(4) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281
(*) Corresponding Author

Abstract


Mahkota dewa (Phaleria macrocarpa (Scheff.) Boerl.) which is belong to family of Thymelaeaceae is one of Indonesian traditional medicines. Chemical constituent has been isolated from bark of mahkota dewa. Sample was extracted with methanol. Concentrated methanol extract was extracted by n-hexane, chloroform and ethyl acetate. A Compound that separated and purified by column chromatography from ethyl acetate extract is a red spherical crystal (m.p. 94-95 °C). Its spot gave yellow fluorescence at TLC plate (UV366) and has optical rotation of -9.3°(c. 2 mg/mL, methanol). Structure elucidation by UV, IR, 1H-NMR, 13C-NMR and NMR 2 dimension (HMQC, COSY, HMBC and DEPT-135) spectroscopy show that the compound gives a name macronone. Computational chemistry calculation using Hyperchem on the level of semiempirical method PM3 was confirmed the conformation of macronone. DPPH method shows that macronone has lower antioxidant activity compare to the ethyl acetate extract.

Keywords


macronone; diepoxylignan; mahkota dewa; Phaleria macrocarpa (Scheff.) Boerl.; DPPH

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References

[1] Harmanto, N., 2005, Mahkota dewa, Gods Heritage Drugs, 1ST Ed., Agro Media Pustaka, Jakarta.

[2] Oshimi, S., Zaima, K., Matsuno, Y., Hirasawa, Y., Iizuka, T., Studiawan, H., Indrayanto, G., Zaini, N.C., and Morita, H., 2008, J. Nat. Med., 62, 2, 207–210.

[3] Lisdawati, V., Wiryowidagdo, S., Kardono, L., and Broto, S., 2007, Buletin Penelitian Kesehatan, 35, 3, 115–124.

[4] Kurnia, D., Akiyama, K., and Hiyashi, H., 2008, Biosci. Biotechnol. Biochem., 72, 2, 618–620.

[5] Zhang, Y.B., Yu, X.J., and Liu, H.M., 2006, J. Asian Nat. Prod. Res., 8, 1-2, 119–123.

[6] Hartati, M.S., Mubarika, S., Gandjar, I.G., Hamann, M.T., Rao, K.V., and Wahyuono, S., 2005, Indo. J. Pharm., 16, 1, 51–57.

[7] Susilawati, Matsjeh, S., Pranowo, H.D., and Anwar, C., 2011, Indo. J. Chem., 11, 2, 180–185.

[8] Winarno, H., and Katrin W.E, 2009, Indo. J. Chem., 9, 1, 142–145.

[9] Saufi, A, 2007, Lignan in Phaleria macrocarpa (Scheff.,) Boerl., Inaugural-Dissertation, Düsseldorf, Germany.

[10] Ullah, N., Ahmeed, S., Muhammad, P., Ahmed, Z., Nawaz, H.R., and Malik, A., 1999, Phytochemistry, 51, 103–105.

[11] Molyneux, P., 2004, Songklanakarin J. Sci. Technol., 26, 2, 211–219.

[12] Creswell, C.J., Runquist, O.A., and Campbell, M.M., 2005, Spectral Analysis of Organic Compounds, 10th ed., ITB, Bandung, Indonesia.

[13] Silverstein, R.M., Bassler, G.C., Morrill, and T.C., 2005. Spectrometric Identification Organic Compounds, 7th ed., New York: John Wiley and Sons Inc.



DOI: https://doi.org/10.22146/ijc.21373

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

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