Abstract
Although a number of chemicals have been isolated from Terminalia arjuna, only a few have been evaluated for their biological significance. As a part of our drug discovery programme for cytotoxic agents from Indian medicinal plants, four novel cytotoxic agents arjunic acid (1), arjungenin (2), arjunetin (3) and arjunoglucoside I (4) were isolated from the bark of T. arjuna. Out of the four compounds, arjunic acid (1) was significantly active against the human oral (KB), ovarian (PA 1) and liver (HepG-2 & WRL-68) cancer cell lines. Further, the most active compound arjunic acid was converted into seven semi-synthetic ester derivatives 5-11. 2-O-Palmitoyl arjunic acid (6) showed two times more activity, while 2,3-di-O-acetyl-, 2-O-p-anisoyl-, 2,3-di-O-benzoyl- and 2, 3-di-O-p-nitrobenzoyl arjunic acid (7-10) showed 1.7-2.3 times less activity than the cytotoxic drug vinblastine against the liver cancer cell lines HepG-2 and WRL-68 respectively. © Georg Thieme Verlag KG Stuttgart.
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Saxena, M., Faridi, U., Mishra, R., Gupta, M. M., Darokar, M. P., Srivastava, S. K., … Khanuja, S. P. S. (2007). Cytotoxic agents from Terminalia arjuna. Planta Medica, 73(14), 1486–1490. https://doi.org/10.1055/s-2007-990258
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