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Isolation and Identification of Triterpenoids from Flowers of Lawsonia inermis
Corresponding Author(s) : Jiang Liu
Asian Journal of Chemistry,
Vol. 26 No. 14 (2014): Vol 26 Issue 14
Abstract
A new oleanane-type triterpenoid, 2a, 3b-dihydroxyolean-18-en-28-oic acid (3) along with five known triterpenoids, b-sitosterol (1), oleanolic acid (2), crataegolic acid (4), alphitolic acid (5) and colosolic acid (6) were isolated from the flowers of Lawsonia inermis. Their structures were elucidated by spectroscopic analyses.
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- G. Chaudhary and S. Goyal, Int. J. Pharm. Sci. Drug Res., 2, 91 (2010).
- D. Prakash, S. Suri, G. Upadhyay and B.N. Singh, Int. J. Food Sci. Nutr., 58, 18 (2007); doi:10.1080/09637480601093269.
- P. Muthumani and R. Meera, Res. J. Pharm. Technol., 3, 736 (2010).
- J.-R. Liou, M. El-Shazly, Y.-C. Du, C.-N. Tseng, T.-L. Hwang, Y.-L. Chuang, Y.-M. Hsu, P.-W. Hsieh, C.-C. Wu, S.-L. Chen, M.-F. Hou, F.-R. Chang and Y.-C. Wu, Phytochemistry, 88, 67 (2013); doi:10.1016/j.phytochem.2012.11.010.
- A. Ostovari, S.M. Hoseinieh, M. Peikari, S.R. Shadizadeh and S.J. Hashemi, Corros. Sci., 51, 1935 (2009); doi:10.1016/j.corsci.2009.05.024.
- A.B. Hsouna, M. Trigui, G. Culioli, Y. Blache and S. Jaoua, Food Chem., 125, 193 (2011); doi:10.1016/j.foodchem.2010.08.060.
- A.E. Musa, A.T. Selvi, R. Aravindhan, B. Madhan, A. Fathima and J.R. Rao, Am. Leather Chem. Assoc., 106, 170 (2011).
- M. Trigui, A. Ben Hsouna, I. Hammami, G. Culioli, M. Ksantini, S. Tounsi and S. Jaoua, Crop Prot., 45, 83 (2013); doi:10.1016/j.cropro.2012.11.014.
- Y.-C. Chang and F.-R. Chang, Chin. Chem. Soc., 47, 373 (2000).
- S.H. Wu, Y.B. Ma, X.D. Luo and X.J. Hao, Zhongcaoyao, 33, 679 (2002).
- J.C.A. Tanaka, G.J. Vidotti and C.C. Silva, J. Braz. Chem. Soc., 14, 475 (2003); doi:10.1590/S0103-50532003000300024.
- H.-Y. Gao and L.-J. Wu, Zhongguo Tianran Yaowu, 1, 82 (2003).
- J.-J. Cheng, L.-J. Zhang, H.-L. Cheng, C.-T. Chiou, I.J. Lee and Y.-H. Kuo, J. Nat. Prod., 73, 1655 (2010); doi:10.1021/np1003593.
- A.G. González, B.M. Fraga, P. González, M.G. Hernandez and A.G. Ravelo, Phytochemistry, 20, 1919 (1981); doi:10.1016/0031-9422(81)84035-6.
- A. De Felice, A. Bader, A. Leone, S. Sosa, R. Loggia, A. Tubaro and N. De Tommasi, Planta Med., 72, 643 (2006); doi:10.1055/s-2006-931573.
References
G. Chaudhary and S. Goyal, Int. J. Pharm. Sci. Drug Res., 2, 91 (2010).
D. Prakash, S. Suri, G. Upadhyay and B.N. Singh, Int. J. Food Sci. Nutr., 58, 18 (2007); doi:10.1080/09637480601093269.
P. Muthumani and R. Meera, Res. J. Pharm. Technol., 3, 736 (2010).
J.-R. Liou, M. El-Shazly, Y.-C. Du, C.-N. Tseng, T.-L. Hwang, Y.-L. Chuang, Y.-M. Hsu, P.-W. Hsieh, C.-C. Wu, S.-L. Chen, M.-F. Hou, F.-R. Chang and Y.-C. Wu, Phytochemistry, 88, 67 (2013); doi:10.1016/j.phytochem.2012.11.010.
A. Ostovari, S.M. Hoseinieh, M. Peikari, S.R. Shadizadeh and S.J. Hashemi, Corros. Sci., 51, 1935 (2009); doi:10.1016/j.corsci.2009.05.024.
A.B. Hsouna, M. Trigui, G. Culioli, Y. Blache and S. Jaoua, Food Chem., 125, 193 (2011); doi:10.1016/j.foodchem.2010.08.060.
A.E. Musa, A.T. Selvi, R. Aravindhan, B. Madhan, A. Fathima and J.R. Rao, Am. Leather Chem. Assoc., 106, 170 (2011).
M. Trigui, A. Ben Hsouna, I. Hammami, G. Culioli, M. Ksantini, S. Tounsi and S. Jaoua, Crop Prot., 45, 83 (2013); doi:10.1016/j.cropro.2012.11.014.
Y.-C. Chang and F.-R. Chang, Chin. Chem. Soc., 47, 373 (2000).
S.H. Wu, Y.B. Ma, X.D. Luo and X.J. Hao, Zhongcaoyao, 33, 679 (2002).
J.C.A. Tanaka, G.J. Vidotti and C.C. Silva, J. Braz. Chem. Soc., 14, 475 (2003); doi:10.1590/S0103-50532003000300024.
H.-Y. Gao and L.-J. Wu, Zhongguo Tianran Yaowu, 1, 82 (2003).
J.-J. Cheng, L.-J. Zhang, H.-L. Cheng, C.-T. Chiou, I.J. Lee and Y.-H. Kuo, J. Nat. Prod., 73, 1655 (2010); doi:10.1021/np1003593.
A.G. González, B.M. Fraga, P. González, M.G. Hernandez and A.G. Ravelo, Phytochemistry, 20, 1919 (1981); doi:10.1016/0031-9422(81)84035-6.
A. De Felice, A. Bader, A. Leone, S. Sosa, R. Loggia, A. Tubaro and N. De Tommasi, Planta Med., 72, 643 (2006); doi:10.1055/s-2006-931573.