Isolation of Taxifolin from Trichilia Emetica Whole Seeds
Keywords:
Trichilia emetica, Taxifolin, Meliaceae, Spectroscopy, Limonoids.Abstract
Taxifolin was isolated from the boiled water extract of Trichilia emetica whole seeds. The structure was determined by IR, 1H and 13C NMR and mass spectroscopic methods, as well as comparison of the data obtained with that reported in the literature.
References
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[2] B.M. Komane, E.I. Olivier, A.M. Viljoen, Trichilia emetica (Meliaceae) - A review of traditional uses, biological activities and phytochemistry. Phytochem. Lett. 4, 1–9, 2011.
[3] M. Traore, L. Zhai, M. Chen, C.E. Olsen, N. Odile, G.I. Pierre, O.J. Bosco, G.T. Robert, S.B. Christensen, Cytotoxic kurubasch aldehyde from Trichilia emetica. Nat. Prod. Res. 21, 13–17, 2007.
[4] M. Nakatani, J.C. James, K. Nakanishi, Structure of Limonoid Antifeedant from Trichilia roka. Phytochemistry 24, 195–196, 1985.
[5] M. Nakatani, J.C. James, K. Nakanishi, Isolation and structures of Trichilins, Antifeedants against the Southern Army Worms. J. Am. Chem. Soc. 103, 1228–1230. 1981.
[6] A.A.L. Gunatilaka, V.S. Bolzani, E. Dagne, G.A. Hofmann, R.K. Johnson, F.L. Mccabe, M.R. Mattern, D.G.I.Kingston, Limonoids Showing Selective Toxicity to DNA Repaire-Deficient Yeast and Other Constituents of Trichilia emetica. J. Nat. Prod. 61, 179–184. 1998.
[7] H.A. Van der Vossen, G.S. Mkamilo, 2007. Vegetable oils of tropical Africa, conclusion and recommendations based on PROTA 14: “Vegetable oils”. Available on: PROTA (Plant Resources of Tropical Africa/Resources vegetales de I’Afrique tropicale), Wageningen, Netherlands http://www.prota.co.ke/en/p. PROTA.
[8] D. Diallo, B.S. Paulsen, T.H.A. Liljeback, T.E. Michaelsen. The malian medicinal plant Trichilia emetica; studies on polysaccharides with complement fixing ability. J. Ethnopharmacol. 84, 279–287. 2003.
[9] L.Y. Foo, J.J. Karchesy. Polyphenolic glycosides from Douglas fir inner bark. Phytochemistry 28, 1237–1240, 1989.
[10] K. Ishimaru, G. Nonaka, I. Nishioka. Flavan-3-ol and procyanidin glycosides from Quercus miyagii. Phytochemistry 26, 1167–1170. 1987.
[11] U. Takahama, R. Yamauchi, S. Hirota. Isolation and characterization of a cyanidin-catechin pigment from adzuki bean (Vigna angularis). Food Chem. 141, 282–288. 2013.
[12] M.H. Oh, K.H. Park, M.H. Kim, H.H. Kim, K.J. Park, J.H. Heo, M.W. Lee, Anti-oxidative and anti-inflammatory effects of phenolic compounds from the stems of Quercus acuta Thunberg. Asian J. Chem. 26, 4582–4586. 2014.
[13] H.X. Han, S.S. Hong, S.J. Hwang, K.M. Lee, Y.B. Hwang, S.J. Ro. Monoamine oxidase inhibitory components from Cayratia japonica. Arch Pharm Res 30, 13–17. 2007.
[14] L. Wang, X. Li, S. Zhang, W. Lu, S. Liao, X. Liu, L. Shan, X. Shen, H. Jiang, W. Zhang, J. Huang, H. Li. Natural products as a gold mine for selective matrix metalloproteinases inhibitors. Bioorganic Med. Chem. 20, 4164–4171. 2012.
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Published
2016-06-29
How to Cite
Usman, A., Thoss, V., & Nur-e-Alam, M. (2016). Isolation of Taxifolin from Trichilia Emetica Whole Seeds. American Scientific Research Journal for Engineering, Technology, and Sciences, 21(1), 77–82. Retrieved from https://asrjetsjournal.org/index.php/American_Scientific_Journal/article/view/1370
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