Phytochemical Investigation of the Roots of Jatropha Integerrima Jacq
Abstract
Jatropha integerrima Jacq. (Euphorbiaceae), is grown in many tropical and subtropical countries and used to treat eczema, herpes, ringworm, rheumatism, pruritus, scabies, toothaches, tumors and warts. Its latex is toxic. A methanolic extract of the roots was chromatographed over silica gel column packed in petroleum ether. The column was eluted with petroleum ether, chloroform and methanol successively in order of increasing polarity to isolate n-pentadecanyl oleate (1), α-D-glucopyranosyl-(2→1')-O-α-D-glucopyranoside (α-D-diglucoside, 2), n-hexanoyl-O- α -D-glucopyranosyl-(2a→1b)-O- α -D-glucopyranosyl-(2b→1c)-O- α -D-glucopyranosyl-(2c→1d)-O- α -D-glucopyranosyl-(2d→1e)-O- α -D-glucopyranoside (n-caproyl O-α-D-pentaglucoside, 3), n-hexanoyl-O-β-D-glucopyranosyl-(2a→1b)-O-β-D-glucopyranosyl-(2b→1c)-O-β-D-glucopyranosyl-(2c→1d)-O-β-D-glucopyranosyl-(2d→1e)-O-β-D-glucopyranosyl-(2e→1f)-O-β-D-glucopyranoside (n-caproyl O-β-D-hexaglucoside, 4), α -D-glucopyranosyl-(2→1a)-O- α -D-glucopyranosyl-(2a→1b)-O- α -D-glucopyranosyl-(2b→1c)-O- α -D-glucopyranosyl-(2c→1d)-O- α -D-glucopyranosyl-(2d→1e)-O- α -D-glucopyranoside (α-D-hexaglucoside 5) and α -D-glucopyranosyl-(2→1a)-O- α -D-glucopyranosyl-(2a→1b)-O- α -D-glucopyranosyl-(2b→1c)-O- α -D-glucopyranosyl-(2c→1d)-O- α -D-glucopyranosyl-(2d→1e)-O- α -D-glucopyranosyl-(2e→1f)-O- α -D-glucopyranoside (α-D-heptaglucoside, 6) . The structures of these compounds have been established on the basis of spectral data analysis and chemical means.
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References
E.F. Gilman and D.G. Watson , 1993, Jatropha integerrima (Peregrina), Environmental Horticulture Department, University of Florida.
N.P. Balakrishnan and T. Chakrabarty, 2007, The Family Euphorbiaceae in India: A synopsis of its profile, taxonomy and bibliography. Bishen Singh Mahendra Pal Singh, Dehradun.
P.R. Krishnan and M. Paramathma, 2009, Current Science, 97, 1000-1004.
K.R. Kirtikar and B.D. Basu, 2002, Indian Medicinal Plants. Popular Prakashan, Dehradun, 1570-1579.
S. Sharma, S. Parveen, A. Malik and M.R.K. Sherwani, 2013, International Journal of Pharmacy and Chemical Science, 2, 1971 – 1973.
S. Sutthivaiyakit , W. Mongkolvisut, P. Ponsitipiboon, S. Prabpai, P. Kongsaeree, S. Ruchirawatb and C. Mahidol, 2003, Tetrahedron Letters, 44, 3637–3640.
W. Mongkolvisut, S. Sutthivaiyakit, H. Leutbecher, S. Mika, I. Klaiber, W. Möller, H. Rösner, U. Beifuss and J. Conder, 2006, Journal of Natural Products, 69, 1435-1441.
N. Idrissa, D. Adama, B. Mamadou, S.G. Rokhaya , T. Yoro, W. Alassane and F. Djibril , 2016, Journal of Chemical and Pharmaceutical Research, 8, 135- 139.
A. Welé, C. Baraguèye, W. Ndiaye, D. Fall, I. Ndoye, Y. Diop, L. Dubosq and B. Bodo , 2007, Dakar Med. 52, 209 – 215.
A.O. Eshilokun , K. Adeleke, I.A. Ogunwande and W.N. Setzer, 2007, Natural Product Communications, 2, 853-855 •
J.Y. Zhu, B. Cheng , Y.J. Zheng, Z. Dong, S.-L. Lin , G.-H. Tang, Q. Gu and S. Yin, 2015, RSC Advances. An international journal to further the chemical sciences, 16, 11697-12479.
S. Sutthivaiyakit , W. Mongkolvisut , S. Prabpai and P. Kongsaeree , 2009, J Nat Prod, 72, 2024 -2027.
F.T. Zohora, P. Sarkar, F.S. Tareq, F. Islam, C.M. Hasan and M. Ahsan, 2013, Asian Journal of Chemistry, 25, 2853-2856.
S.K. Sharma and H. Singh, 2013, Der Pharmacia Lettre, 5, 155-159.
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