In vitro Anti-Leishmanial and Anti-Tumour Activities of a Pentacyclic Triterpenoid Compound Isolated from the Fruits of Dregea volubilis Benth Asclepiadaceae
Purpose: Dregea volubilis Benth , commonly known as Jukti in Bengal, is used in the treatment of boils and abscesses from ancient times. The purpose of this study is to elucidate the active compounds and as well as their anti-leishmanial and anti-tumour activities. Methods: Dried and crushed fruits...
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Veröffentlicht in: | Tropical journal of pharmaceutical research 2009-07, Vol.8 (2) |
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Sprache: | eng |
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Zusammenfassung: | Purpose: Dregea volubilis Benth , commonly known as Jukti in
Bengal, is used in the treatment of boils and abscesses from ancient
times. The purpose of this study is to elucidate the active compounds
and as well as their anti-leishmanial and anti-tumour activities.
Methods: Dried and crushed fruits of Dregea volubilis were extracted
by petroleum ether (40 -60°C); the best solvent system had first
been verified by analytical Thin Layer Chromatography (TLC). The
extract was subjected to TLC and column chromatography (CC) to isolate
the pure compounds. Spectra data were obtained by Infra Red
pectroscopy, Mass Spectroscopy and Nuclear Magnetic Resonance -Proton
Magnetic Resonance (PMR), Carbon Magnetic Resonance (CMR) and
Distortionless Enhancement by Polarization Transfer (DEPT) -for
structure elucidation of the isolated compound(s). One of the compounds
isolated was screened for anti-leishmanial activity against
promastigotes of Leishmania donovani and anti-tumour activity on K562
leukemic cell line. Results: A pentacyclic triterpenoid compound was
isolated and designated as taraxerone, and then characterized as
d-friedoolean-14-en, 3 one together with ß-sitosterol and a long
chain lipid fraction.. This compound showed in vitro anti-leishmanial
activity against promastigotes of Leishmania donovani (strain AG 83)
and anti-tumour activity on K562 leukemic cell line. Conclusion: A
pentacyclic triterpenoid compound designated as taraxerone and
characterized as Dfriedoolean-14-en, 3 one together was successfully
isolated. The structure was determined on the basis of spectral
analysis (IR, MASS, NMR (PMR, CMR and DEPT) and the compound
demonstrated in vitro anti-leishmanial and anti-tumour activities. |
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ISSN: | 1596-5996 1596-9827 |
DOI: | 10.4314/tjpr.v8i2.44520 |