Skip to main content
Log in

Chemical constituents from the aerial parts ofLippia nodiflora linn.

  • Article
  • Drug discovery
  • Published:
Archives of Pharmacal Research Aims and scope Submit manuscript

Abstract

Phytochemical investigation of the methanolic extract of the aerial parts ofLippia nodiflora Linn, led to the isolation of a new triterpenoid lippiacin (1) and a benzofuranone rengyolone (halleridone,2) through repeated silica gel column chromatography and semi preparative HPLC. The structures of these compounds were determined by spectroscopic methods, including 1D and 2D NMR, as well as by comparison with published data. A complete assignment of the1H- and13C-NMR data of2 is reported based on 2DNMR (COSY-45,HMQC and HMBC) spectroscopic methods.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Basu, A. K., Chakraborti, P., and Sanyal, P. K., Nodifloretin-A new flavone from itLippi nodifloria.J. Ind. Chem. Soc., 46, 271–272 (1969).

    Google Scholar 

  • Bianco, A., Scalzo, R. L., and Scarpati, M. L., Isolation of cornoside fromOlea europaea and its transformation into halleridone.Phytochemistry, 23, 455–457 (1993).

    Article  Google Scholar 

  • Budzikiewicz, H., Wilson, J. M., and Djerassi, C., Mass spectrometry in structural and stereo chemical problems pentacyclic triterpenes.J. Am. Chem. Soc., 85, 3688- 3699 (1963).

    Article  CAS  Google Scholar 

  • Chopra, R. N., Nayar, S. L., and Chopra, I. C., Glossary of Indian Medicinal Plants, Council of Scientific and Industrial Research, New Delhi, p.155 (1956).

    Google Scholar 

  • Endo, K. and Hikino, H., Structures of rengyol, rengyoxide, and rengyolone, new cyclo-hexylethane derivatives fromForsythia suspense fruit.Can. J. Chem., 62,2011 (1984).

    Article  CAS  Google Scholar 

  • Forestieri, A. M., Monforte, M. T., Ragusa, S., Trovato, A., and Lauk, L., Antiinflammatory, analgesic and antipyretic activity in rodents of plant used in African medicine.Phytoth. Res., 10, 100–106 (1996).

    Article  CAS  Google Scholar 

  • Francisco, A., Barbaran, T., Harborne, B. J., and Self, R., Twelve 6-oxygenated flavone sulphates fromLippia nodiflora andL. canescens.Phytochemistry, 26, 2281–2284 (1987).

    Article  Google Scholar 

  • Hooker, J. D., The Flora British India,L. Reve and Co. 5, Henrietta Street, Covent Garden, London, Vol. IV, P. 563 (1885).

  • Jayaweera, D. M. A., Medicinal Plants (Indigenous and Exotic Used in Ceylon), The National Science Council of Srilanka, Colombo, Part V, p. 169 (1982).

    Google Scholar 

  • Kirtikar, K. R., The Indian Medicinal plants, Sudhindra Nath Basu, M.B. Panini: Office 13 Bhuwaneswari Asrama Bahadur Gang, Allahabad, Part-11, pp.986–987 (1918).

    Google Scholar 

  • Knight, S. A., Carbon-13 NMR spectra of some tetra- and pentacyclic triterpenoids.Org. Mag. Reson., 6, 603–611 (1974).

    Article  CAS  Google Scholar 

  • Manjunath, B. L., The Wealth of India, Council of Scientific and Industrial Research, New Delhi, India, Vol. VI, pp. 142–143 (1962).

    Google Scholar 

  • Messana, I., Sperandei, M., Multari, G., Galeffi, C., and Bettolo, G. B. M., A cyclohexadie-none and cyclohexenone fromHalleria lucida.Phytochemistry, 23, 2617–2619 (1984).

    Article  CAS  Google Scholar 

  • Nair, A. G. R., Ramesh, P., Nagarajan, S., and Subramanian, S., New flavone glycosides fromLippia nodifloria.Ind. J. Chem., 2, 1316–1317 (1973).

    Google Scholar 

  • Riaz, N., Anis, I., Rehman, A., Malik, A., Ahmed, Z., Muhammad, P., Shujaat, S., and Rahaman, A., Emodinol, β-Glucuronidase inhibiting triterpene fromPaeonia emodi.Nat. Prod. Res., 17, 247–251 (2003).

    Article  PubMed  CAS  Google Scholar 

  • Seo, S., Tomita, Y., and Tori, K., Biosynthesis of oleanene- and ursene- type triterpenes from [4-13C] mevalonolactone and [1, 2-13C2] acetate in tissue cultures ofIsodon japonicus HaraJ. Am. Chem. Soc., 103, 2075–2080 (1981).

    CAS  Google Scholar 

  • Siddiqui, B. S., llyas, F., Rasheed, M., and Begum, S., Chemical constituents of leaves and stem bark ofPlumeria obtuse.Phytochemistry, 65, 2077–2084 (2004).

    Article  PubMed  CAS  Google Scholar 

  • Tori, K., Seo, S., Shimaoka, A., and Tomita, Y., Carbon-13 NMR spectra of olean-12-enes. Full signal assignment including quaternary carbon signals assigned by use of indirect13C,1H spin couplings.Tet. Lett., 48, 4227–4230 (1974).

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bina S. Siddiqui.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Siddiqui, B.S., Ahmad, F., Sattar, F.A. et al. Chemical constituents from the aerial parts ofLippia nodiflora linn.. Arch Pharm Res 30, 1507–1510 (2007). https://doi.org/10.1007/BF02977318

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02977318

Key words

Navigation