A NEW CYTOTOXIC DOLABELLANE FROM THE INDONESIAN SOFT CORAL Anthelia sp.

https://doi.org/10.22146/ijc.21279

Anggia Murni(1), Novriyandi Hanif(2*), Junichi Tanaka(3)

(1) Biopharmaca Research Center, Bogor Agricultural University, Kampus IPB Taman Kencana, Jl. Taman Kencana No. 3, Bogor 16128
(2) Department of Chemistry, Faculty of Mathematic and Natural Sciences, Bogor Agricultural University, Jl. Agatis Wing 2 Level 4, Bogor 16144
(3) Department of Chemistry, Biology and Marine Science, University of the Ryukyus Nishihara, Okinawa 903-0213
(*) Corresponding Author

Abstract


One new dolabellane (1) and two known diterpenoids stolonidiol (2) and clavinflol B (3) have been isolated from the ethyl acetate extract of the Indonesian soft coral Anthelia sp. A new compound 1 exhibited a moderate cytotoxicity against NBT-T2 cells at 10 µg/mL, while known compounds 2 and 3 showed cytotoxicity at 1 and 0.5 µg/mL, respectively. Structure of the new compound 1 was elucidated by interpretation of NMR spectroscopic data (1D and 2D NMR data) and mass spectrometry (ESIMS data) as well as comparison with those of related ones. This finding should be useful for anti cancer drug development of the promising dolabellane-types compound.

Keywords


Anthelia sp.; soft coral; dolabellane; NBT-T2; cytotoxicity; marine

Full Text:

Full Text PDF


References

[1] Uemura, D., Han, C., Hanif, N., Inuzuka, T., Maru, N., and Arimoto, H., 2012, Pure Appl. Chem., 86, 6, 1297–1315.

[2] Tanaka, J., Kuniyoshi, M., Tanaka, C., Issa, H.H., Balansa, W., Otsuka, M., Githige, W.P., and Higa, T., 2005, Pure Appl. Chem., 77, 1, 83–89.

[3] Blunt, J.W., Copp, B.R., Keyzers, R.A., Munro, M.H.G., and Prinsep, M.R., 2013, Nat. Prod. Rep., 30, 2, 237–323.

[4] Bordeleau, M-E., Mori, A., Oberer, M., Lindqvist, L., Chard, L.S., Higa, T., Belsham, G.J., Wagner, G., Tanaka, J., and Pelletier, J., 2006, Nat. Chem. Biol., 2, 4, 213–220.

[5] Kashman, Y., and Rudi, A., 2004, Phytochem. Rev., 3, 3, 309–323.

[6] Lin, Y-S., Fazary, A.E., Chen, C-H., Kuo, Y-H., and Shen, Y-C., 2011, Helv. Chim. Acta, 94, 2, 273–281.

[7] Mushti, C.S., Kim, J-H., and Corey, E.J., 2006, J. Am. Chem. Soc., 128, 43, 14050–14052.

[8] Kim, B.J., Nam, J.H., Kwon, Y.K., So, I., and Kim, S.J., 2013, Basic Clin. Pharmacol. Toxicol., 112, 2, 83–89.

[9] Hanif, N., Tanaka, J., Setiawan, A., Trianto, A., de Voogd, N.J., Murni, A., Tanaka, C., and Higa, T., 2007, J. Nat. Prod., 70, 3, 432–435.

[10] Mori, K., Iguchi, K., Yamada, N., Yamada, Y., and Inouye, Y., 1987, Tetrahedron Lett., 28, 46, 5673–5676.

[11] Shen, Y-C., Pan, Y-L., Ko, C-L.; Kuo, Y-H., and Chen, C-Y., 2003, J. Chin. Chem. Soc., 50, 3A, 471–476.



DOI: https://doi.org/10.22146/ijc.21279

Article Metrics

Abstract views : 2144 | views : 1796


Copyright (c) 2013 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.