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Type :article
Subject :Q Science (General)
Main Author :Hanita Omar
Additional Authors :Mehran Fadaeinasab
Hairin Tahad
Aty Widyawaruyantie
Mohd Azlan Nafiah
Tiah Rachmatiah
Title :Aporphine alkaloids with in vitro antiplasmodial activity from the leaves of Phoebe tavoyana
Place of Production :Tanjong Malim
Publisher :Fakulti Sains dan Matematik
Year of Publication :2020
Corporate Name :Universiti Pendidikan Sultan Idris

Abstract : Universiti Pendidikan Sultan Idris
One new aporphine named tavoyanine A (1), along with four known aporphines laetanine (2), roemerine (3), laurolitsine (4), and boldine (5), and one morphinandienone type sebiferine (6) were isolated from the leaves of Phoebe tavoyana (Meissn.) Hook f. (Lauraceae). The isolation was achieved by chromatographic techniques, and the structural elucidation was performed via spectral methods. This paper also reports the antiplasmodial activity of roemerine (3), laurolitsine (4), boldine (5), and sebiferine (6). The results showed that 3–6 have a potent inhibitory activity against the growth of Plasmodium falciparum 3D7 clone, with IC50 values of 0.89, 1.49, 1.65, and 2.76 µg/ml, respectively.

References

[1] WHO Global Malarial Programme, World Malaria Report (World Health Organization, Geneva, 2014), p. 50.

[2] J. Wiesner and R. Ortmann, Angew. Chem. Int. Ed. Engl. 42, 5274 (2003). Crossref. PubMed.

[3] B. Greenwood and T. Mutabingwa, Nature 415, 670 (2002). Crossref. PubMed.

[4] D.J. Wyler, Clin. Infect. Dis. 16, 449 (1993). Crossref. PubMed.

[5] H.N. Ridley, The Flora of Malay Peninsular (L. Reeve & Co., Amsterdam, 1967), p. 103.

[6] E.H. Corner, Wayside Trees of Malaya, 3rd ed. (Malaysian Nature Society, 1988), p. 34.

[7] K.M. Kochummen, Tree Flora (Forest Research Institute Malaysia, Kepong, Selangor, 1989), p. 98.

[8] H. Omar and M.H. Najihah, Molecules 18, 8994 (2013). Crossref. PubMed.

[9] K. Awang and M.R. Mukhtar, Nat. Prod. Res. 21, 704 (2007). Crossref. PubMed.

[10] H. Guinaudeau and M. Leboeuf, J. Nat. Prod. 46, 761 (1983). Crossref.

[11] M. You and D.B. Wickramaratne, J. Nat. Prod. 58, 598 (1995). Crossref. PubMed.

[12] D.W. Hughes and K. Genest, J. Pharm. Sci. 57, 1619 (1968). Crossref. PubMed.

[13] S. Hernan and B.K. Cassels, J. Pharmacol. Res. 29, 1 (1994). Crossref. PubMed.

[14] A. Mollataghi and H. A. Hadi, Molecules 17, 4197 (2012). Crossref. PubMed.

[15] S. Goodwin and J.N. Shooley, Proc. Chem. Soc. 3, 306 (1958).

[16] M. Shamma and W. Slusarchyk, Chem. Rev. 64, 59 (1964). Crossref.

[17] N. Borthakur and R.C. Rastogi, Phytochemistry 18, 910 (1979). Crossref.

[18] M. Fadaeinasab and H. Taha, Nat. Prod. Commun. 10, 1541 (2015). PubMed.

[19] K. Likhitwitayawuid and C.K. Angerhofer, J. Nat. Prod. 56, 30 (1993). Crossref. PubMed.

[20] Y. Zuguang and D.Y. Knox, Malar. Control Elimination 5, 1 (2015).

[21] S. Saxena and N. Pant, Curr. Sci. 85, 1314 (2003).

[22] W. Trager and J.B. Jensen, Science 20, 673 (1976). Crossref.

[23] A. Budimulya and S. Syafruddin, Mol. Biochem. Parasitol. 184, 137 (1997). Crossref.

 


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