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Abstract : Universiti Pendidikan Sultan Idris |
A phytochemical investigation of the stem bark of Calophyllum canum resulted in the isolation of a new xanthone dimer identified as biscaloxanthone (1), together with four compounds; trapezifoliaxanthone (2), trapezifolixanthone A (3), taraxerone (4) and taraxerol (5). The structures of these compounds were determined via spectroscopic methods of IR, UV, MS and NMR (1D and 2D). The cytotoxicity of compounds 1-3 were screened against A549, MCF-7, C33A and 3T3L1 cell lines, wherein weak cytotoxic activities were observed (IC50 > 50 ?m). 2020 Walter de Gruyter GmbH, Berlin/Boston 2020. |
References |
Alkhamaiseh, S. I., Taher, M., Ahmad, F., Qaralleh, H., Althunibat, O. Y., Susanti, D., & Ichwan, S. J. A. (2012). The phytochemical content and antimicrobial activities of malaysian calophyllum canum (stem bark). Pakistan Journal of Pharmaceutical Sciences, 25(3), 555-563. Retrieved from www.scopus.com Carpenter, I., Locksley, H. D., & Scheinmann, F. (1969). Extractives from guttiferae. part X. the isolation and structure of four xanthones from calophyllum canum hook f. Journal of the Chemical Society C: Organic, (3), 486-488. doi:10.1039/j39690000486 Dharmaratne, H. R. W., Napagoda, M. T., & Tennakoon, S. B. (2009). Xanthones from roots of calophyllum thwaitesii and their bioactivity. Natural Product Research, 23(6), 539-545. doi:10.1080/14786410600899118 Kar Wei, L., Zamakshshari, N. H., Ee, G. C. L., Mah, S. H., & Mohd Nor, S. M. (2018). Isolation and structural modifications of ananixanthone from calophyllum teysmannii and their cytotoxic activities. Natural Product Research, 32(18), 2147-2151. doi:10.1080/14786419.2017.1367781 Lemos, L. M. S., Oliveira, R. B., Sampaio, B. L., Ccana-Ccapatinta, G. V., Da Costa, F. B., & Martins, D. T. O. (2016). Brasiliensic and isobrasiliensic acids: Isolation from calophyllum brasiliense cambess. and anti-helicobacter pylori activity. Natural Product Research, 30(23), 2720-2725. doi:10.1080/14786419.2015.1137568 Li, Z. -., Liu, D., Li, D. -., & Hua, H. -. (2011). A novel prenylated xanthone from the stems and leaves of calophyllum inophyllum. Natural Product Research, 25(9), 905-908. doi:10.1080/14786419.2010.513977 Lim, C. K., Subramaniam, H., Say, Y. H., Jong, V. Y. M., Khaledi, H., & Chee, C. F. (2015). A new chromanone acid from the stem bark of calophyllum teysmannii. Natural Product Research, 29(21), 1970-1977. doi:10.1080/14786419.2015.1015020 Lim, S. C., Lemmens, R., & Calophyllum, L. (1993). In Timber Trees-Major Commercial Timbers, , 114-132. Retrieved from www.scopus.com Mah, S. H., Ee, G. C. L., Teh, S. S., & Sukari, M. A. (2015). Calophyllum inophyllum and calophyllum soulattri source of anti-proliferative xanthones and their structure-activity relationships. Natural Product Research, 29(1), 98-101. doi:10.1080/14786419.2014.959949 Nasir, N. M., Rahmani, M., Shaari, K., Ee, G. C. L., Go, R., Kassim, N. K., . . . Iskandar, M. J. (2011). Two new xanthones from calophyllum nodusum (guttiferae). Molecules, 16(11), 8973-8980. doi:10.3390/molecules16118973 Nasir, N. M., Rahmani, M., Shaari, K., Kassim, N. K., Go, R., Stanslas, J., & Jeyaraj, E. J. (2013). Xanthones from calophyllum gracilipes and their cytotoxic activity. Sains Malaysiana, 42(9), 1261-1266. Retrieved from www.scopus.com Nguyen, L. -. T., Nguyen, D. M., & Nguyen, L. -. D. (2013). A new xanthone from the bark of calophyllum thorelii. Natural Product Research, 27(6), 563-567. doi:10.1080/14786419.2012.682992 Salleh, W. M. N. H. W., Ahmad, F., Khong, H. Y., Zulkifli, R. M., Chen, J. -., Nahar, L., . . . Sarker, S. D. (2016). Beilschglabrines A and B: Two new bioactive phenanthrene alkaloids from the stem bark of beilschmiedia glabra. Phytochemistry Letters, 16, 192-196. doi:10.1016/j.phytol.2016.04.013 Salleh, W. M. N. H. W., Razak, N. Z. A., & Ahmad, F. (2017). Phytochemicals and biological activities of macaranga hosei and macaranga constricta (euphorbiaceae). Marmara Pharmaceutical Journal, 21(4), 881-888. doi:10.12991/mpj.2017.11 Susanti, D., Sirat, H. M., Ahmad, F., Ali, R. M., Aimi, N., & Kitajima, M. (2007). Antioxidant and cytotoxic flavonoids from the flowers of melastoma malabathricum L. Food Chemistry, 103(3), 710-716. doi:10.1016/j.foodchem.2006.09.011 Wezeman, T., Bräse, S., & Masters, K. -. (2015). Xanthone dimers: A compound family which is both common and privileged. Natural Product Reports, 32(1), 6-28. doi:10.1039/c4np00050a |
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