Cycloartane Glycosides from the Roots of Cimicifuga foetida with Wnt Signaling Pathway Inhibitory Activity
- PMID: 25693500
- PMCID: PMC4402585
- DOI: 10.1007/s13659-015-0053-7
Cycloartane Glycosides from the Roots of Cimicifuga foetida with Wnt Signaling Pathway Inhibitory Activity
Abstract
Four new 9,19-cycloartane triterpenoids, cimilactone E (1), cimilactone F (2), 2'-O-(E)-butenoyl-23-epi-26-deoxyactein (3), and 2',12β-O-diacetylcimiracemonol-3-O-β-d-xylopyranoside (4), together with four known constituents (5-8) were isolated from the roots of Cimicifuga foetida. The new structures were elucidated by extensive spectroscopic analysis. In addition, compounds 7 and 8 showed significant Wnt signaling pathway inhibitory activity, with IC50 values of 3.33 and 13.34 μM, respectively, using the luciferase reporter gene assay.
Keywords: 9,19-Cycloartane triterpenoids; Cimicifuga foetida; Cimilactone-type; Luciferase activity; Wnt signal pathway.
Conflict of interest statement
All authors declare no conflict of interest.
Figures
Similar articles
-
Cytotoxic chemical constituents from the roots of Cimicifuga foetida. [corrected].J Nat Prod. 2010 Feb 26;73(2):93-8. doi: 10.1021/np9003855. J Nat Prod. 2010. PMID: 20121210
-
[Cycloartane triterpenoid of Cimicifuga foetida].Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1930-4. Zhongguo Zhong Yao Za Zhi. 2009. PMID: 19894537 Chinese.
-
Cimicifoetisides A and B, two cytotoxic cycloartane triterpenoid glycosides from the rhizomes of Cimicifuga foetida, inhibit proliferation of cancer cells.Beilstein J Org Chem. 2007 Jan 31;3:3. doi: 10.1186/1860-5397-3-3. Beilstein J Org Chem. 2007. PMID: 17266751 Free PMC article.
-
Photochemistry and pharmacology of 9, 19-cyclolanostane glycosides isolated from genus Cimicifuga.Chin J Nat Med. 2016 Oct;14(10):721-731. doi: 10.1016/S1875-5364(16)30087-5. Epub 2016 Oct 31. Chin J Nat Med. 2016. PMID: 28236402 Free PMC article. Review.
-
[Studies on the constituents of Cimicifuga species].Yakugaku Zasshi. 2001 Jul;121(7):497-521. doi: 10.1248/yakushi.121.497. Yakugaku Zasshi. 2001. PMID: 11494597 Review. Japanese.
Cited by
-
Anticancer Chemodiversity of Ranunculaceae Medicinal Plants: Molecular Mechanisms and Functions.Curr Genomics. 2017 Feb;18(1):39-59. doi: 10.2174/1389202917666160803151752. Curr Genomics. 2017. PMID: 28503089 Free PMC article. Review.
-
New potential beneficial effects of actein, a triterpene glycoside isolated from Cimicifuga species, in breast cancer treatment.Sci Rep. 2016 Oct 12;6:35263. doi: 10.1038/srep35263. Sci Rep. 2016. PMID: 27731376 Free PMC article.
-
A Systems Biology-Based Investigation into the Pharmacological Mechanisms of Sheng-ma-bie-jia-tang Acting on Systemic Lupus Erythematosus by Multi-Level Data Integration.Sci Rep. 2015 Nov 12;5:16401. doi: 10.1038/srep16401. Sci Rep. 2015. PMID: 26560501 Free PMC article.
-
Six New 9,19-Cycloartane Triterpenoids from Cimicifuga foetida L.Nat Prod Bioprospect. 2016 Aug;6(4):187-93. doi: 10.1007/s13659-016-0097-3. Epub 2016 May 20. Nat Prod Bioprospect. 2016. PMID: 27207314 Free PMC article.
-
Cytotoxic Cycloartane Triterpenoid Saponins from the Rhizomes of Cimicifuga foetida.Nat Prod Bioprospect. 2019 Aug;9(4):303-310. doi: 10.1007/s13659-019-0214-1. Epub 2019 Jun 18. Nat Prod Bioprospect. 2019. PMID: 31214880 Free PMC article.
References
-
- Li XY, Wang YY, Yuan CG, Hao XJ, Li Y. Nat. Prod. Bioprospect. 2013;3:24–28. doi: 10.1007/s13659-012-0094-0. - DOI
-
- Pharmacopoeia Commission of the People’s Republic of China . The Pharmacopoeia of Chinese People’s Republic. Beijing: The Chemical Industry Publishing House; 2010. pp. 68–69.
LinkOut - more resources
Full Text Sources
Other Literature Sources