APHORPINE ALKALOIDS FROM BARK OF Cryptocarya ferrea

https://doi.org/10.22146/ijc.21516

Nurdin Saidi(1*), A. Hamid A. Hadi(2), Khalijah Awang(3), Mat Ropi Mukhtar(4)

(1) Department of Chemistry, Faculty of Mathematics and Natural Sciences, Syiah Kuala University, Banda Aceh, 23111
(2) Department of Chemistry, Faculty of Science, University of Malaya K. Lumpur
(3) Department of Chemistry, Faculty of Science, University of Malaya K. Lumpur
(4) Department of Chemistry, Faculty of Science, University of Malaya K. Lumpur
(*) Corresponding Author

Abstract


Isolation, identification and characterization of the compounds isolated from the bark of Cryptocarya ferrea yielded three known aphorpine alkaloids. They are (-)-O-methylisopiline 1, (+)-norlirioferine 2 and (+)-lirioferine 3. Structural elucidation was established through several spectroscopic methods, such as 1D-NMR (1H, 13C, DEPT, NOE), 2D-NMR (COSY, NOESY, HMQC, HMBC), UV, IR, and MS and comparison with the published data.


Keywords


Cryptocarya ferrea; (-)-o-methylisopiline; (+)-norlirioferine; (+)-lirioferine

Full Text:

Full Text PDF


References

[1] Lee, S.S., Lin, Y.J., Chen, C.K., Liu, K.S., and Chen, C.H., 1993, J. Nat. Prod., 56, 11, 1971-1976.

[2] Lee, S.S., Chen, C.H., and Liu, Y.C., 1993, J. Nat. Prod., 56, 2, 227-232.

[3] Lin, F.W., Wu, P.L., and Wu, T.S., 2001, Chem. Pharm. Bull., 49, 10, 1292-1294.

[4] Bick, I.R.C., Sevenet, T., Sinchai, W., Skelton, B.W., and White, A.H., 1981, Aust. J. Chem., 34, 195-200.

[5] Lamberton, J.A., and Vashist, V.N., 1972, Aust. J. Chem., 25, 2737-2738.

[6] Borthakur, N., Mahanta, P.K., and Rastogi, R.C., 1981, Phytochem., 20, 501-504.

[7] Ohashi, M., Wilson, J.M., Budzikiewicz, H., Shamma, M., Slusarchyk, W.A., and Djerassi, C., 1963, Am. Chem. Soc., 85, 2807-2809.

[8] Chen, C.L., and Chang, H., 1978, Phytochem., 17, 779-782.

[9] Connolly, J.D., Haque, M.E., and Kadir, A.A., 1996, Phytochem., 43, 1, 779-782.

[10] Chen, C.H., Chang, H.M., Cowling, E.B., Hsu, C.Y.H., and Gates, R.P., 1976, Phytochem., 15, 1161-1167.

[11] Castro, O.C., Lopes, J.L., and Vergera, A.G., 1985, Phytochem., 24, 1, 203-204.

[12] Marsaioli, A.J., Reis, F., de A.M., Magalhaes, A.F., and Ruveda, E.A., 1979, Phytochem., 18, 165-169.

[13] Smolnycki, W.D., Maniot, J.L., Hindenlang, D.M., Miana, G.A., and Shamma, M., 1978, Tetrahedron Lett., 47, 4617-4620.

[14] Shamma, M., 1960, Experienta, 16, 484.



DOI: https://doi.org/10.22146/ijc.21516

Article Metrics

Abstract views : 1261 | views : 1243


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.