Terpenoids from Chloranthus elatior

doi:10.1007/s13659-012-0039-7

Natural Products and Bioprospecting ›› 2012, Vol. 2 ›› Issue (4): 156-159.DOI: 10.1007/s13659-012-0039-7

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Terpenoids from Chloranthus elatior

Chang-Li SUN^a,b, Huan YAN^a, Xu-Hong LI^a, Xue-Fang ZHENG^a, Hai-Yang LIU^a

a State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
b College of Forestry, Southwest Forestry University, Kunming 650224, China

Received:2012-05-21 Revised:2012-06-25 Online:2018-02-11 Published:2012-08-24
Supported by:
This work was supported by National Natural Science Funding of China(No. 81072543), the Key Project of Knowledge Innovation Project of CAS(No. KSCX2-EWQ-10), and funds(No. P2009-KF04) from the State Key Laboratory of Phytochemistry and Plant Resources in West China.

Terpenoids from Chloranthus elatior

Chang-Li SUN^a,b, Huan YAN^a, Xu-Hong LI^a, Xue-Fang ZHENG^a, Hai-Yang LIU^a

a State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
b College of Forestry, Southwest Forestry University, Kunming 650224, China

通讯作者: Hai-Yang LIU,E-mail:haiyangliu@mail.kib.ac.cn
基金资助:
This work was supported by National Natural Science Funding of China(No. 81072543), the Key Project of Knowledge Innovation Project of CAS(No. KSCX2-EWQ-10), and funds(No. P2009-KF04) from the State Key Laboratory of Phytochemistry and Plant Resources in West China.

Abstract

Abstract: Two new eudesmane-type sesquiterpenoid lactones, named chlorelactone A(1) and chlorelactone B(2), and one new labdane-type diterpenoid, named elatiorlabdane(3), along with seven known sesquiterpenoids and one known disesquiterpenoid were isolated from the whole plants of Chloranthus elatior. Their structures and relative configurations were established on the basis of extensive spectroscopic analysis.

Key words: Chloranthus elatior, Chloranthaceae, sesquiterpenoid, chlorelactone, elatiorlabdane

摘要： Two new eudesmane-type sesquiterpenoid lactones, named chlorelactone A(1) and chlorelactone B(2), and one new labdane-type diterpenoid, named elatiorlabdane(3), along with seven known sesquiterpenoids and one known disesquiterpenoid were isolated from the whole plants of Chloranthus elatior. Their structures and relative configurations were established on the basis of extensive spectroscopic analysis.

关键词: Chloranthus elatior, Chloranthaceae, sesquiterpenoid, chlorelactone, elatiorlabdane

Chang-Li SUN, Huan YAN, Xu-Hong LI, Xue-Fang ZHENG, Hai-Yang LIU. Terpenoids from Chloranthus elatior[J]. Natural Products and Bioprospecting, 2012, 2(4): 156-159.

Chang-Li SUN, Huan YAN, Xu-Hong LI, Xue-Fang ZHENG, Hai-Yang LIU. Terpenoids from Chloranthus elatior[J]. 应用天然产物, 2012, 2(4): 156-159.

References

[1] Delectis Flora Reipublicae Popularis Sinicae Agendae Academiae Sinicae Edita. Flora of China; Science Press:Beijing, 1982, 20(1), pp 80-95.
[2] Zhou, Z. K. Acta Bot. Yunnan. 1993, 15, 321-331.
[3] Editorial committee of the Administration Bureau of Traditional Chinese Medicine. Chinese Matrria Medica (Zhonghua Bencao); Shanghai Press of Science and Technology:Shanghai, 1998, 3, pp 449-450.
[4] Cao, C. M.; Peng, Y.; Shi, Q. W.; Xiao, P. G. Chem. Biodivers. 2008, 5, 219-238.
[5] Teng, F.; Zhong, H. M.; Chen, C. X.; Liu, H. Y. Helv. Chim. Acta 2009, 92, 1298-1303.
[6] Xiao, Z. Y.; Wang, X. C.; Zhang, G. P.; Huang, Z. L.; Hu, L. H. Helv. Chim. Acta 2010, 93, 803-810.
[7] Fang, P. L.; Liu, H. Y.; Zhong, H. M. Chin. J. Nat. Med. 2012, 10, 24-27.
[8] Wang, F.; Zhou, D. S.; Wei, G. Z.; Ren, F. C.; Liu, J. K. Phytochemistry 2012, 77, 312-317.
[9] Ran, X. H.; Teng, F.; Chen, C. X.; Wei, G.; Hao, X. J.; Liu, H. Y. J. Nat. Prod. 2010, 73, 972-975.
[10] Zhan, Z. J.; Ying, Y. M.; Ma, L. F.; Shan, W. G. Nat. Prod. Rep. 2011, 28, 594-629.
[11] Fang, P. L.; Cao, Y. L.; Yan, H.; Pan, L. L.; Liu, S. C.; Gong, N. B.; Lü, Y.; Chen, C. X.; Zhong, H. M.; Guo, Y.; Liu, H. Y. J. Nat. Prod. 2011, 74, 1408-1413.
[12] Wu, B.; He, S.; Wu, X. D.; Wu, D. K.; Pan, Y. J. Helv. Chim. Acta 2007, 90, 1586-1591.
[13] Wu, B.; He, S.; Wu, X. D.; Pan, Y. J. Chem. Biodivers. 2008, 5, 1298-1303.
[14] Goud, T. V.; Reddy, N. S.; Krishnaiah, P.; Venkateswarlu Y. Biochem. Syst. Ecol. 2002, 30, 493-495.
[15] Chang, F. R.; Huang, T. L.; Chen, Y.; Kuo, R. Y.; Chang, Y. C.; Chiu, H. F.; Wu, Y. C. J. Nat. Prod. 2002, 65, 255-258.
[16] Kusono, G.; Abe, M.; Koike, Y.; Uchida, M.; Nozoe, S.; Taira, Z. Yakugazu Zasshi 1991, 111, 756-764.
[17] Xu, Y. J.; Tang, C. P.; Ke, C. Q.; Zhang, J. B.; Weiss, H. C.; Ye, Y. J. Nat. Prod. 2007, 70, 1987-1990.
[18] Wang, Y. Z.; Tang, C. P.; Ke, C. Q.; Weiss, H. C.; Gesing, E. R.; Ye, Y. Phytochemistry 2008, 69, 518-526.
[19] Li, C. J.; Zhang, D. M.; Luo, Y. M.; Yu, S. S.; Li, Y.; Lu, Y. Phytochemistry 2008, 69, 2867-2874.

Terpenoids from Chloranthus elatior

Terpenoids from Chloranthus elatior

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