Sesquiterpenoids from the Rhizomes of <i>Homalomena occulta</i>

doi:10.1007/s13659-016-0104-8

Natural Products and Bioprospecting

2016, Vol. 6

Issue (4) : 211-216 DOI: 10.1007/s13659-016-0104-8

Original article

Sesquiterpenoids from the Rhizomes of Homalomena occulta

Jun-Li Yang¹, Ya-Min Zhao¹, Yan-Ping Shi^1,2

1. Key Laboratory of Chemistry of Northwestern Plant Resources of CAS and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, People's Republic of China;
2. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, People's Republic of China

Abstract
References
Related Articles
Metrics

Download: PDF(561 KB) HTML ()
Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks

Abstract Naturally occurring oplopanane sesquiterpenoids are rarely reported. A phytochemical investigation on the rhizomes of Homalomena occulta (Lours) has resulted in the discovery of six oplopanane sesquiterpenoids (1-6), including four new (1-4) and one 3,5-seco-oplopanane (6), together with three previously reported sesquiterpenoids (7-9). In addition three new oplopananes (2a-4a) were also obtained by chemical transformation. All structures of these sesquiterpenoids were established based on the comprehensive spectroscopic analyses, including NMR, MS, and IR, and comparing with the literatures.

Keywords Homalomena occulta Sesquiterpenoids Oplopananes

Fund:The work was financially supported by the National Nature Science Foundation of China (Nos.21375136 and 21575150),and the scientific research project of Central Asia Drug Discovery and Development Centre of Chinese Academy of Sciences (No.CAM201404) and the CAS Pioneer Hundred Talents Program

Issue Date: 08 February 2018

	Service

	E-mail this article
	E-mail Alert
	RSS
	Articles by authors

	Jun-Li Yang
	Ya-Min Zhao
	Yan-Ping Shi

Trendmd:

Cite this article:

Jun-Li Yang,Ya-Min Zhao,Yan-Ping Shi. Sesquiterpenoids from the Rhizomes of Homalomena occulta[J]. Natural Products and Bioprospecting, 2016, 6(4): 211-216.

URL:

http://npb.kib.ac.cn/EN/10.1007/s13659-016-0104-8 OR http://npb.kib.ac.cn/EN/Y2016/V6/I4/211

1. Chinese Pharmacopoeia Commission, Chinese Pharmacopoeia (Part I, 2015 Edition), p33, China Medical Science Press (2015)
2. M. Elbandy, H. Lerche, H. Wagner, M.A. Lacaille-Dubois, Biochem. Syst. Ecol. 32, 1209-1213 (2004)
3. Y.M. Hu, C. Liu, K.W. Cheng, H.H.Y. Sung, L.D. Williams, Z.L. Yang, W.C. Ye, Phytochemistry 69, 2367-2373 (2008)
4. Y.M. Hu, Z.L. Yang, H. Wang, W.C. Ye, Nat. Prod. Res. 23, 1279-1283 (2009)
5. X.Y. Tian, Y. Zhao, S.S. Yu, W.S. Fang, Chem. Biodivers. 7, 984-992 (2010)
6. Y.F. Wang, X.Y. Wang, G.F. Lai, C.H. Lu, S.D. Luo, Chem. Biodivers. 4, 925-931 (2007)
7. X.H. Li, W.J. Zhang, H.Y. Qi, Y.P. Shi, Can. J. Chem. 87, 1218-1221 (2009)
8. R. Wang, W.H. Chen, Y.P. Shi, J. Nat. Prod. 73, 17-21 (2010)
9. R. Wang, L.L. Liu, Y.P. Shi, Helv. Chim. Acta 93, 2081-2085 (2010)
10. J.L. Yang, L.L. Liu, Y.P. Shi, Tetrahedron Lett. 50, 6315-6317 (2009)
11. G.Y. Zhu, G.P. Peng, Nat. Prod. Res. Dev. 14, 85-88 (2002)
12. Y.H. Kuo, C.F. Chyu, Tetrahedron Lett. 44, 7221-7223 (2003)
13. T.V. Sung, L. Kutschabsky, A. Porzel, W. Steglich, G. Adam, Phytochemistry 31, 1659-1661 (1992)
14. W. Herz, K. Watanabe, Phytochemistry 22, 1457-1459 (1983)
15. H. Heymann, Y. Tezuka, T. Kikichi, S. Supriyatna, Chem. Pharm. Bull. 42, 138-146 (1994)
16. G.P. Peng, F.C. Lou, Nat. Prod. Res. Dev. 13, 9-11 (2001)
17. G.Y. Zhu, G.P. Peng, Nat. Prod. Res. Dev. 14, 85-88 (2002)
18. Z.F. Li, Z.H. Wu, G. Chen, Q.H. Zhang, Y.H. Pei, J. Asian Nat. Prod. Res. 11, 715-718 (2009)
19. K.C. Wong, A. Hamid, I.M.S. Eldeen, M.Z. Asmawi, S. Baharuddin, H.S. Abdillahi, J. van Staden, Nat. Prod. Res. 26, 850-858 (2012)
20. L.S. Gan, Z.J. Zhan, S.P. Yang, J.M. Yue, J. Asian Nat. Prod. Res. 8, 589-594 (2006)
21. S. Yang, H, Chen. J. Yue Chin. J. Chem. 30, 1243-1248 (2012)
22. H.B. Xu, Y.B. Ma, X.Y. Huang, C.A. Geng, H. Wang, Y. Zhao, T.H. Yang, X.L. Chen, C.Y. Yang, X.M. Zhang, J.J. Chen, J. Ethnopharmacol. 171, 131-140 (2015)
23. G.J. Zhang, Y.H. Li, J.D. Jiang, S.S. Yu, X.J. Wang, P.Y. Zhuang, Y. Zhang, J. Qu, S.G. Ma, Y. Li, Y.B. Liu, D.Q. Yu, Tetrahedron 70, 4494-4499 (2014)
24. L. Zhang, J.H. Zhang, S.M. Yang, C.H. Tan, H.F. Luo, D.Y. Zhu, J. Asian Nat. Prod. Res. 12, 215-219 (2010)
25. Y. Narukawa, C. Komatsu, R. Yamauchi, S. Shibayama, M. Hachisuka, F. Kiuchi, J. Nat. Med. p 1-7, (2016)
26. W. Wang, Z. Ali, X.C. Li, T.A. Smillie, D.A. Guo, I.A. Khan, Fitoterapia 80, 404-407 (2009)
27. N. Liu, X. Yu, H. Zhao, Y. Zhao, Zhongcaoyao 40, 29-32 (2009)

[1]	Michel Feussi Tala, Jianchun Qin, Joseph T. Ndongo, Hartmut Laatsch. New Azulene-Type Sesquiterpenoids from the Fruiting Bodies of Lactarius deliciosus[J]. Natural Products and Bioprospecting, 2017, 7(3): 269-273.
[2]	Ce Kuang, Shu-Xi Jing, Yan Liu, Shi-Hong Luo, Sheng-Hong Li. *Drimane Sesquiterpenoids and Isochromone Derivative from the Endophytic Fungus Pestalotiopsis* sp. M-23**[J]. Natural Products and Bioprospecting, 2016, 6(3): 155-160.
[3]	Xiao-Yan YANG, Tao FENG, Jian-Hai DING, Zheng-Hui LI, Yan LI, Qiong-Ying FAN, Ji-Kai LIU. Two new drimane sesquiterpenoids from cultures of the basidiomycete Trichaptum biforme[J]. Natural Products and Bioprospecting, 2013, 3(4): 154-157.
[4]	Xiao-Yan YANG, Tao FENG, Jian-Hai DING, Xia YIN, Hua GUO, Zheng-Hui LI, Ji-Kai LIU. Five new 5, 6-seco-tremulane sesquiterpenoids from the basidiomycete Conocybe siliginea[J]. Natural Products and Bioprospecting, 2013, 3(2): 48-51.
[5]	Liang-Yan LIU, Zheng-Hui LI, Ze-Jun DONG, Xing-Yao LI, Jia SU, Yan LI, Ji-Kai LIU. Two novel fomannosane-type sesquiterpenoids from the culture of the basidiomycete Agrocybe salicacola[J]. Natural Products and Bioprospecting, 2012, 2(3): 130-132.

Viewed

Full text

Abstract

Cited

Shared

Discussed