New apotirucallane-type triterpenoids from Chisocheton paniculatus

Feng Zhang; Xiu-Feng He; Wen-Bin Wu; Wan-Sheng Chen; Jian-Min Yue

doi:10.1007/s13659-012-0065-5

. 2012 Dec 12;2(6):235–239. doi: 10.1007/s13659-012-0065-5

New apotirucallane-type triterpenoids from Chisocheton paniculatus

Feng Zhang ^1,², Xiu-Feng He ², Wen-Bin Wu ², Wan-Sheng Chen ^1,^✉, Jian-Min Yue ^2,^✉

PMCID: PMC4131609

Graphical abstract

Two new apotirucallane triterpenoids, namely chisiamols G (1) and H (2), featuring a 21,23-lactone, together with five known triterpenoids, were isolated from the twigs of Chisocheton paniculatus. The structures of the new compounds were elucidated on the basis of spectroscopic and chemical methods.

graphic file with name 13659_2012_65_Article_Fig1_HTML.jpg

Electronic Supplementary Material

Supplementary material is available for this article at 10.1007/s13659-012-0065-5 and is accessible for authorized users.

Keywords: Chisocheton paniculatus, apotirucallane triterpenoids, chisiamols G and H

Electronic supplementary material

13659_2012_65_MOESM1_ESM.pdf^{(3.7MB, pdf)}

Supplementary material, approximately 3.74 MB.

Footnotes

This article is published with open access at Springerlink.com

Contributor Information

Wan-Sheng Chen, Email: chenwanshengsmmu@yahoo.com.cn.

Jian-Min Yue, Email: jmyue@mail.shcnc.ac.cn.

References

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

13659_2012_65_MOESM1_ESM.pdf^{(3.7MB, pdf)}

Supplementary material, approximately 3.74 MB.

[CR1] [1] (a).Chen S. K., Li H., Chen P. Y. Flora of China. Beijing: Science Press; 1997. pp. 98–99. [Google Scholar]

[CR2] [1] (b).Mulholland D. A., Parel B., Coombes P. H. Curr. Org. Chem. 2000;4:1011–1054. doi: 10.2174/1385272003375941. [DOI] [Google Scholar]

[CR3] [2] (a).Connolly, J. D.; Labbe, C.; Rycroft, D. S.; Taylor, D. A. H. J. Chem. Soc., Perkin Trans. I1979, 2959–2964.

[CR4] [2] (b).Chatterjee A., Nayak L., Das B., Patra A., Dhara K. P., Mukherjee K., Banerji J. Indian J. Chem., Sect. B. 1989;28:231–236. [Google Scholar]

[CR5] [2] (c).Bordoloi M., Saikia B., Mathur R. K., Goswami B. N. Phytochemistry. 1993;34:583–584. doi: 10.1016/0031-9422(93)80054-V. [DOI] [Google Scholar]

[CR6] [2] (d).Yadav R. D., Kataky J. C. S., Mathur R. K. Indian J. Chem., Sect. B. 1999;38:243–245. [Google Scholar]

[CR7] [2] (e).Sarmah G. K., Bhattacharyya N. K., Goswami B. N., Barua P., Kataky J. C. S. J. Indian Chem. Soc. 2003;80:1163–1168. [Google Scholar]

[CR8] [2] (f).Awang K., Lim C. S., Mohamad K., Morita H., Hirasawa Y., Takeya K., Thoison O., Hadi A. H. Bioorg. Med. Chem. 2007;15:5997–6002. doi: 10.1016/j.bmc.2007.05.049. [DOI] [PubMed] [Google Scholar]

[CR9] [2] (g).Maneerat W., Laphookhieo S., Koysomboon S., Chantrapromma K. Phytomedicine. 2008;15:1130–1134. doi: 10.1016/j.phymed.2008.05.004. [DOI] [PubMed] [Google Scholar]

[CR10] [2] (h).Phongmaykin J., Kumamoto T., Ishikawa T., Suttisri R., Saifah E. Arch. Pharm. Res. 2008;31:21–27. doi: 10.1007/s12272-008-1115-8. [DOI] [PubMed] [Google Scholar]

[CR11] [2] (i).Laphookhieo S., Maneerat W., Koysomboon S., Kiattansakul R., Chantrapromma K., Syers J. K. Can. J. Chem. 2008;86:205–208. doi: 10.1139/v07-155. [DOI] [Google Scholar]

[CR12] [2] (j).Mohamad K., Hirasawa Y., Litaudon M., Awang K., Hadi A. H., Takeya K., Ekasari W., Widyawaruyanti A., Zaini N. C., Morita H. Bioorg. Med. Chem. 2009;17:727–730. doi: 10.1016/j.bmc.2008.11.048. [DOI] [PubMed] [Google Scholar]

[CR13] [2] (k).Xie B. J., Yang S. P., Zhang C., Yue J. M. Chin. J. Chem. 2009;27:1805–1810. doi: 10.1002/cjoc.200990304. [DOI] [Google Scholar]

[CR14] [2] (l).Yang M. H., Wang J. S., Luo J. G., Wang X. B., Kong L. Y. J. Nat. Prod. 2009;72:2014–2018. doi: 10.1021/np900485t. [DOI] [PubMed] [Google Scholar]

[CR15] [2] (m).Yang M. H., Wang J. S., Luo J. G., Wang X. B., Kong L. Y. Can. J. Chem. 2012;90:199–204. doi: 10.1139/v11-147. [DOI] [Google Scholar]

[CR16] [3].Jolad S. D., Hoffmann J. J., Cole J. R. J. Org. Chem. 1980;45:3132–3135. doi: 10.1021/jo01303a044. [DOI] [Google Scholar]

[CR17] [4].Xie B. J., Yang S. P., Chen H. D., Yue J. M. J. Nat. Prod. 2007;70:1532–1535. doi: 10.1021/np0702842. [DOI] [PubMed] [Google Scholar]

[CR18] [5].Zi W. W., Yu S. Y., Ma D. W. Angew. Chem. Int. Ed. 2010;49:5887–5890. doi: 10.1002/anie.201002299. [DOI] [PubMed] [Google Scholar]

[CR19] [6].Pan L., Chin Y. W., Chai H. B., Ninh T. N., Soejarto D. D., Kinghorn A. D. Bioorg. Med. Chem. 2009;17:2219–2224. doi: 10.1016/j.bmc.2008.10.076. [DOI] [PMC free article] [PubMed] [Google Scholar]

[CR20] [7].Kwon D. H., Kato M., El-Zaatari F. A. K., Osato M. S., Graham D. Y. FEMS Microbiol. Lett. 2000;188:197–202. doi: 10.1111/j.1574-6968.2000.tb09193.x. [DOI] [PubMed] [Google Scholar]

PERMALINK

New apotirucallane-type triterpenoids from Chisocheton paniculatus

Feng Zhang

Xiu-Feng He

Wen-Bin Wu

Wan-Sheng Chen

Jian-Min Yue

Graphical abstract

Electronic Supplementary Material

Electronic supplementary material

Footnotes

Contributor Information

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

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PERMALINK

New apotirucallane-type triterpenoids from Chisocheton paniculatus

Feng Zhang

Xiu-Feng He

Wen-Bin Wu

Wan-Sheng Chen

Jian-Min Yue

Graphical abstract

Electronic Supplementary Material

Electronic supplementary material

Footnotes

Contributor Information

References

Associated Data

Supplementary Materials

ACTIONS

PERMALINK

RESOURCES

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