Abstract
Three new ent-kauranoids, isorosthornins A-C (1–3), and a new natural product, dihydroponicidin (4), together with five known ones were isolated from the aerial parts of Isodon rosthornii. The structures were determined by means of extensive spectroscopic analysis. All diterpenoids isolated were evaluated for their cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, and SW480 cell lines, and compounds 5 and 7 showed significant inhibitory effects on all cell lines. 
Electronic Supplementary Material
Supplementary material is available for this article at 10.1007/s13659-011-0031-7 and is accessible for authorized users.
Keywords: Isodon rosthornii, ent-kaurane diterpenoid, cytotoxicity
Electronic supplementary material
Supplementary material, approximately 590 KB.
Footnotes
This article is published with open access at Springerlink.com
Contributor Information
Jian-Xin Pu, Email: pujianxin@mail.kib.ac.cn.
Han-Dong Sun, Email: hdsun@mail.kib.ac.cn.
References
- [1].Sun H. D., Xu Y. L., Jiang B. Diterpenoids from Isodon Species. Beijing: Science Press; 2001. [Google Scholar]
- [2].Sun H. D., Huang S. X., Han Q. B. Nat. Prod. Rep. 2006;23:673–698. doi: 10.1039/b604174d. [DOI] [PubMed] [Google Scholar]
- [3].Academia Sinca. Botany of China. Beijing: Science Publishing House; 1979. [Google Scholar]
- [4] (a).Hu, K.; Dong, A. J.; Kobayashi, H.; Iwasaki, S.; Yao, X. S. Plant Deriv. Antimycotics2003, 525–549
- [4] (b).Kubo I., Xu Y. L., Shimizu K. Phytother. Res. 2004;18:180–183. doi: 10.1002/ptr.1421. [DOI] [PubMed] [Google Scholar]
- [4] (c).Li G. Y., Wang Y. L. Yaoxue Xuebao. 1984;19:590–592. [Google Scholar]
- [4] (d).Xu Y. L., Li Z. Q. Yunnan Zhiwu Yanjiu. 1998;20:97–101. [Google Scholar]
- [4] (e).Xu Y. L., Ma Y. B. Phytochemistry. 1989;28:3235–3237. doi: 10.1016/0031-9422(89)80316-4. [DOI] [Google Scholar]
- [5] (a).Wang X. R., Wang H. P., Hu H. P., Sun H. D., Wang S. Q., Ueda S., Kuroda Y., Fujita T. Phytochemistry. 1995;38:921–926. doi: 10.1016/0031-9422(94)00474-8. [DOI] [Google Scholar]
- [5] (b).Fujita, E.; Taoka, M.; Shibuya, M.; Fujita, T.; Shingu, T., J. Chem. Soc., Perkin Trans. 11973, 2277–2281.
- [6].Hou A. J., Li M. L., Jiang B., Lin Z. W., Ji S. Y., Zhou Y. P., Sun H. D. J. Nat. Prod. 2000;63:599–601. doi: 10.1021/np9903705. [DOI] [PubMed] [Google Scholar]
- [7].Gao Y. H., Wu S. H., Zhong R. J., Li G. Y. Zhongcaoyao. 1996;27:579–580. [Google Scholar]
- [8].Gao Y. H., Wu S. H., Cheng Y. Zhongcaoyao. 1999;30:407–409. [Google Scholar]
- [9].Monks A., Scudiero D., Skehan P., Shoemaker R., Paull K., Vistica D., Hose C., Langley P. J. Natl. Cancer Inst. 1991;83:757–766. doi: 10.1093/jnci/83.11.757. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Supplementary material, approximately 590 KB.
