Phytochemical Investigation of the Roots of Jatropha Integerrima Jacq
Authors/Creators
- 1. Department of Pharmaceutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar – 125 001 (Haryana), India
- 2. Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi 110 062, India
- 3. Present address: College of Pharmacy, Jazan University, Jazan, Saudi Arabia
Description
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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