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GC-MS Analysis of Bioactive Compounds from Bark and Leaf of Boswellia ovalifoliolata
Corresponding Author(s) : Nallani Chakravarthula Sarada
Asian Journal of Chemistry,
Vol. 30 No. 1 (2018): Vol 30 Issue 1
Abstract
The aim of the present study was to identify and characterize the bioactive compounds present in bark and leaf of Boswellia ovalifoliolata using GC-MS analysis. A total of 17 fatty acids methyl ester, i.e., tetradecanoic acid, 12-methyl-, methyl ester (0.9 %), (s)-, hexadecanoic acid, methyl ester (7.6 %), octadecanoic acid, methyl ester (15.0 %) and triacontanoic acid, methyl ester (6.1 %) was identified and characterized. GC-MS analysis of crude extract showed the presence of 31 compounds, i.e., b-amyrin (8.5 %), a-amyrin (29.2 %), stigmasterol (1.5 %), DL-a-tocopherol (7.3 %), b-sitosterol (10.4 %) and vitamin E (2.3 %). This is the first report on the identification of active molecule from different extracts of bark and leaf of Boswellia ovalifoliolata. All the major compounds identified in Boswellia ovalifolilolata are biologically active molecules.
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- D. Gomathi, M. Kalaiselvi, G. Ravikumar, K. Devaki and C. Uma, J. Food Sci. Technol., 52, 1212 (2015); https://doi.org/10.1007/s13197-013-1105-9.
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- M.Z. Siddiqui, Indian J. Pharm. Sci., 73, 255 (2011); https://doi.org/10.4103/0250-474X.93507.
- R. Chib, M. Kumar, M. Rizvi, S. Sharma,A. Pandey, S. Bani, S.S. Andotra, S.C. Taneja and B.A. Shah, RSC Adv., 4, 8632 (2014); https://doi.org/10.1039/c3ra46412a.
- S.L. Deore and S.S. Khadabadi, Phcog. Res., 2, 343 (2010); https://doi.org/10.4103/0974-8490.75452.
- L.H. Vazquez, J. Palazon, A.N. Ocana, in ed.: V. Rao, The Pentacyclic Triterpenes α,β-Amyrins:A Review of Sources and Biological Activities, In: Phytochemicals-A Global Perspective of Their Role in Nutrition and Health, InTech, Chap. 23. pp. 487-502 (2012).
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References
D. Gomathi, M. Kalaiselvi, G. Ravikumar, K. Devaki and C. Uma, J. Food Sci. Technol., 52, 1212 (2015); https://doi.org/10.1007/s13197-013-1105-9.
B.B. Mishra and V.K. Tiwari, Eur. J. Med. Chem., 46, 4769 (2011); https://doi.org/10.1016/j.ejmech.2011.07.057.
J. Balunas and A.D. Kinghorn, Life Sci., 78, 431 (2005); https://doi.org/10.1016/j.lfs.2005.09.012.
G.S. Citoglu and O.B. Acikara, in ed.: S. Dhanarasu, Column Chromatography for Terpenoids and Flavonoids, In: Chromatography and Its Applications, InTech, pp. 13-50 (2012).
D.H. Geetha, M. Rajeswari and I. Jayashree, Asian Pac. J. Trop. Biomed., 3, 985 (2013); https://doi.org/10.1016/S2221-1691(13)60190-2.
I.V. Rodrigues, J.N. de P. Souza,A.C.G. Silva, L.A. Chibli, V.A.R. Cabral, S.A. Viera Filho, F.F. Perazzo, A.G. Guimarães and G.H.B. de Souza, Pharmacogn. J., 5, 6 (2013); https://doi.org/10.1016/j.phcgj.2012.08.001.
M.Z. Siddiqui, Indian J. Pharm. Sci., 73, 255 (2011); https://doi.org/10.4103/0250-474X.93507.
R. Chib, M. Kumar, M. Rizvi, S. Sharma,A. Pandey, S. Bani, S.S. Andotra, S.C. Taneja and B.A. Shah, RSC Adv., 4, 8632 (2014); https://doi.org/10.1039/c3ra46412a.
S.L. Deore and S.S. Khadabadi, Phcog. Res., 2, 343 (2010); https://doi.org/10.4103/0974-8490.75452.
L.H. Vazquez, J. Palazon, A.N. Ocana, in ed.: V. Rao, The Pentacyclic Triterpenes α,β-Amyrins:A Review of Sources and Biological Activities, In: Phytochemicals-A Global Perspective of Their Role in Nutrition and Health, InTech, Chap. 23. pp. 487-502 (2012).
S. Panda, M. Jafri,A. Kar and B.K. Meheta, Fitoterapia, 80, 123 (2009); https://doi.org/10.1016/j.fitote.2008.12.002.
W. Maya, K. Mayur and S. Ashar, Int. J. Pharm. Chem. Sci., 1, 674 (2012).