Phytochemical investigation and isolation of new compounds from the stems of Tinospora cordifolia Miers

  1. Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi- 110062, India | College of Pharmacy, Jazan University, Jazan, Saudi Arabia
  2. Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi- 110062, India
  3. 1-F/O PHARMACY, DEPT OF PHARMACOGNOSY, JAMIA HAMDARD UNIVERSITY, NEW DELHI 2-Phytochemistry Research Laboratory, Faculty of Pharmacy, Jamia Hamdard, New Delhi- 110062, India

Revised: 2017-06-08

Accepted: 2017-07-10

Published in Issue 2017-06-01

How to Cite

Sultana, S., Ali, M., & Jameel, M. (2017). Phytochemical investigation and isolation of new compounds from the stems of Tinospora cordifolia Miers. Trends in Phytochemical Research, 1(2), 83-92. https://oiccpress.com/tpr/article/view/11689

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Abstract

Tinospora cordifolia (Willd.) Miers, (Menispermaceae), a glabrous, deciduous and trailing plant found in tropical India, China, Sri Lanka, Bangladesh and Myanmar. It is used to treat anemia, debility, diabetes, diarrhea, dysentery, dyspepsia, fevers, jaundice, rheumatism, urinary and skin diseases and snake bites. Its air-dried stem powder was exhaustively extracted with methanol. The concentrated methanolic extract was adsorbed on silica gel (60-120 mesh) for the preparation of a slurry. The dried slurry 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 a variety of new chemical constituents characterized as trans-cinnamoyl 2-n-hexanyl-7-methoxynaphthyl amide (2), trans-cinnamoyl 2-n- pentanyl- 6,7- dimethoxynaphthyl amide (3), trans-cinnamoyl 2-n-octanyl-7-methoxynaphthyl amide (4), β-D-arabinosyl-O-geranilan-10′-oate (5), 4,5,7-trimethoxy-2-naphthol-2-O-α-L- arabinofuranosyl-(2′→1′′)-O-α-L-arabinopyranosyl-2′′-O-pentane (6), 5,7-dimethoxy-2-naphthol-2-O-α-L-arabinopyranosyl-(2′→1′′)-α-L- arabinopyranosyl-2′′-O-decane (7) and 5-hydroxy-4''-methoxy-7- flavanoxy- (7→7'''')- β-O-labdan-1-en-3''''α,19''''-olide-18''''-oic acid (tinolabdenyl flavanone) (8) along with cetyl alcohol (1). The structures of all the isolated phytoconstituents have been established on the basis of spectral data analysis and chemical reactions.

Keywords

  • chemical constituents,
  • stems,
  • <i>Tinospora cordifolia</i>,
  • isolation,
  • Characterization