Abstract
Three terpenoids, including two diterpenes (curcusone B and jatrophone) and a triterpene (stigmasterol) have been isolated from the stem bark of Jatropha plants. Curcusone B and stigmasterol were isolated from J. curcas, meanwhile jatrophone and stigmasterol were from J. gossypifolia. The biological activities of these compounds have been evaluated toward bacteria, fungi and tumour cells. Isolation was carried out in vacuum liqiud cromatography (VLC) technique with silica gel as an adsorben and some solvents as eluents. The compound structures were determined by spectroscopic methodes i.e. UV-vis, FTIR, NMR (1-D, 2-D) and were then compared based on their spectroscopic data with similiar data from literatures. The biological properties of these compounds were evaluated against four strains of bacteria (Acetobacter sp., Eschericia coli, Staphylococcus aureus, and Streptococcus sp.), 4 strains of fungi (Aspergilus niger, Penicillium sp. (grey), Penicillium sp. (white) and Rhizopus sp.) and murine leukemia P-388 cells. The results showed that cytotoxic property of curcusone B towards murine leukemia P-388 cells is better than jatrophone and stigmasterol which are IC50 = 0.57 μg/mL (1.93 μM) for curcusone B and IC50 > 100 μg/mL for jatrophone and stigmasterol. Meanwhile, activities against bacteria, jatrophone is better than curcusone B and stigmasterol. Jatrophone is the most active against S. aureus (bacteria) with growth inhibition zone 36 mm and A.niger (fungi) is 44 mm. Further study indicated that jatrophone was bacteriostatic against S. aureus.
References
[1] W. Haas, M. Mittelbach, Ind. Crop. Prod. 12 (2000) 111. [2] T. Iwasaki, Medical Herbs Index in Indonesia, 2nd ed., PT. Eisai Indonesia, Jakarta, 1995, p.97. [3] T. Tang, L. Yin, J. Yang, G. Shan, Eur. J. Pharmacol. 567 (2007) 177. [4] A.A. Gbolade, J. Ethnopharmacol. 121 (2009) 135. [5] M.K. Ali, P.M. Leddet, S. Hutter, S. Ainouddin, S. Hassani, Y. Ibrahim, N. Azas, E. Ollivier, J. Ethnopharmacol. 116 (2008) 74. [6] Sahidin, Ruslin, A. Zaeni, S. Raharjo, Laporan Penelitian Universitas Haluoleo, Kendari, 2008, p.28. [7] D. Sukumaran, B.D. Parashar, A.K. Gupta, K. Jeevaratnam, S. Prakash, Mem. Inst. Oswaldo Cruz 99/2 (2004) 205. [8] R. Dabur, A. Gupta, T.K. Mandal, D.D. Singh, V. Bajpai, A.M. Gurav, G.S. Lavekar, Afr. J. Trad. CAM 4/3 (2007) 313. [9] S.B. Kosalge, R.A. Pursule, J. Ethnopharmacol. 121 (2009) 456 [10] A.M. Mujumdar, A.V. Mistar, J. Ethnopharmacol. 90 (2004) 11. [11] O. Osoniyi, F. Onajobi, J. Ethnopharmacol. 89 (2003) 101. [12] B. Das, A. Kashinathan, R. Reddy, Biochem. Syst. Ecol. 31 (2003) 1189. [13] N. Ravindranath, C. Ramesh, B. Das, Biochem. Syst. Ecol. 31(2003) 431. [14] W. Naengchomnong, P. Wiriyachitra, J. Clardy, Tetrahedron Lett. 27 (1986) 2439. [15] L. Jie-Qing, Y. Yuan-Feng, W. Cui-Fang, L. Yan, Q. Ming-Hua, Tetrahedron xxx (2012 in press) 1-5. [16] M.O.F. Goulart, A.E.G. Sant’Ana, R.A. Lima, S.H. Cavalcante, M.G. Carvalho, F.R. Braz, Quím. Nova 16 (1993) 95. [17] B. Das, A. Kashinatham, B. Venkataiah, K.V.N.S. Srinavas, G. Mahendar, M.R. Reddy, Biochem. Syst. Ecol. 31 (2003) 1189. [18] P. Thakurta, P. Bhowmik, S. Mukherjee, T.K. Hajra., A. Patra., P.K. Bag, J. Ethnopharmacol. 111 (2007) 607. [19] S.H. Cho, J.H. Choi, K.S. Chung, D.H. Kim, K.T. Lee, BMC Cancer 9 (2009) 449. [20] M. Pertino, G.S. Hirschmann, L.S. Santos, J.A. Rodriguez, C. Theoduloz, Z. Naturforsch 62b (2007) 275. [21] Sahidin, S. Nakazibwe, M. Taher, A.K. Saxena, S.J. A. Ichwan, Ardiansyah, Aust. J. Basic Appl. Sci. 5 (2011) 47.
Recommended Citation
Sahidin, Sahidin; Ardiansyah, Ardiansyah; Muhammad, Taher; and Marianti, Manggau
(2011)
"TERPENOIDS FROM THE STEM BARK OF JATROPHA PLANTS AND THEIR BIOLOGICAL ACTIVITIES,"
Makara Journal of Science: Vol. 15:
Iss.
2, Article 18.
Available at:
https://scholarhub.ui.ac.id/science/vol15/iss2/18