A STIGMASTEROL GLYCOSIDE FROM THE ROOT WOOD OF Melochia Umbellata (Houtt) Stapf var. degrabrata K.

https://doi.org/10.22146/ijc.21379

Ahmad Ridhay(1), Alfian Noor(2*), Nunuk H. Soekamto(3), Tjodi Harlim(4), Ian van Altena(5)

(1) Department of Chemistry, Tadulako University, Palu
(2) Department of Chemistry, Hasanuddin University, Makassar 90245
(3) Department of Chemistry, Hasanuddin University, Makassar 90245
(4) Department of Chemistry, Hasanuddin University, Makassar 90245
(5) School of Environmental and Life Science, University of Newcastle, Callaghan, NSW 2308
(*) Corresponding Author

Abstract


A stigmasterol glycoside (stigmast-5,22-dien-3-O-β-D-glucopyranoside) has been isolated from the chloroform fraction of root wood of Melochia umbellata (Houtt) Stapf var. degrabrata K. The compound structure was determined on spectroscopic evidences including IR, 1D and 2D NMR and compared to previous data. The isolate was also active against Aspergillus niger.

Keywords


Melochia umbellata; root wood; stigmasterol glycoside; Aspergillus niger

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References

[1] Mabberley, D.J., 1997, The plant-book: A Portable Dictionary of the vascular Plants, 2nd ed., Cambridge University Press, 874.

[2] Meragelman T.L., Tucker, K.D., McCloud, T.G., Cardellina, J.H., and Shoemaker, R.H., 2005, J. Nat. Prod., 68, 12, 1790–1792.

[3] Bai, H., Li, S., Yin, F., and Hu, L., 2005, J. Nat. Prod., 68, 8, 1159–1163.

[4] Hoelzel, S.C.S.M., Vieira, E.R., Giacomelli, S.R., Dalcol, I.I., Zanatta, N., and Morel, A.F., 2005, Phytochemistry, 66, 10, 1163–1167.

[5] Kapadia, G.J., Paul, B.D., Silverton, J.V., Fales, H.M., and Sokoloski, E.A., 1975, J. Am. Chem. Soc., 97, 23, 6814–6819.

[6] Kapadia, G.J., Shukla, Y.N., Basak, S.P., Henry, M.F., and Sokoloski, E.A., 1978, Phytochemistry, 17, 1444-1445.

[7] Dias, G.C.D., Gressler, V., Hoenzel S.C.S.M., Silva, U.F, Dalcol, I.I., and Morel. A.F., 2007, Phytochemistry, 68, 5, 668–672.

[8] Heyne, K., 1987, Useful Plants in Indonesia, Agency for Forestry Research and Development, Ministry of Forestry, Jakarta, 1345.

[9] Erwin, Noor, A., Soekamto, N.H., and Harlim, T., 2010, Indo. J. Chem., 10, 2, 215–218.

[10] Alam M.S., Chopra, N., Ali, M., and Niwa, M., 1996, Phytochemistry, 41, 4, 1197–1200.

[11] Silverstein, R.M., Bassler, G.C., and Morrill, T.C., 1991, Spectrometric Identification of Organic Compounds, Singapore, 221.



DOI: https://doi.org/10.22146/ijc.21379

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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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