Phytochemical Investigation of the Roots of Jatropha Integerrima Jacq

  • Mohammed Ali Department of Pharmacutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar – 125 001 (Haryana), India.
  • Surinder Kumar Sharma Department of Pharmacutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar – 125 001 (Haryana), India Present address: Herbal Drug Technology, Delhi Pharmaceutical Science and Research University , Puspvihar, Sector 3, New Delhi 110 017, India.
  • Harneet Singh 1Department of Pharmacutical Sciences, Guru Jambheshwar University of Science and Technology, Hisar – 125 001 (Haryana), India
  • Shahnaz Sultnaa Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi 110 062, India. Present address: College of Pharmacy, Jazan University, Jazan, Saudi Arabia.
  • Showkat R. Mir Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi 110 062, India.
Keywords: Jatropha Integerrima, Roots, Chemical Constituents, Isolation, Characterization

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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Published
2017-05-18
How to Cite
Ali, M., Sharma, S., Singh, H., Sultnaa, S., & Mir, S. (2017). Phytochemical Investigation of the Roots of Jatropha Integerrima Jacq. Journal of Progressive Research in Chemistry, 4(3), 194-200. Retrieved from http://scitecresearch.com/journals/index.php/jprc/article/view/1119
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Articles