New Monoterpenoid Indoles with Osteoclast Activities from Gelsemium elegans

被引:9
|
作者
Wei, Xin [1 ]
Guo, Rui [2 ]
Wang, Xiao [1 ,3 ]
Liang, Jia-Jun [1 ]
Yu, Hao-Fei [4 ,5 ]
Ding, Cai-Feng [4 ,5 ]
Feng, Ting-Ting [1 ]
Zhang, Li-Yan [1 ]
Liu, Xia [1 ,3 ]
Hu, Xin-Yue [1 ]
Zhou, Ying [1 ]
机构
[1] Guizhou Univ Tradit Chinese Med, Sch Pharm, Guiyang 550025, Peoples R China
[2] Yunnan Univ Chinese Med, Coll Chinese Mat Med, Kunming 650500, Yunnan, Peoples R China
[3] Guizhou Univ Tradit Chinese Med, Sch Basic Med Sci, Guiyang 550025, Peoples R China
[4] Kunming Med Univ, Sch Pharmaceut Sci, Dept Zool, Kunming 650500, Yunnan, Peoples R China
[5] Kunming Med Univ, Sch Pharmaceut Sci, Yunnan Key Lab Pharmacol Nat Prod, Kunming 650500, Yunnan, Peoples R China
来源
MOLECULES | 2021年 / 26卷 / 24期
基金
中国国家自然科学基金;
关键词
gelselegandines D and E; indole alkaloids; osteoclast cells; Gelsemium elegans; osteoclastogenesis; natural products; ALKALOIDS;
D O I
10.3390/molecules26247457
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The well-known toxic medicine Gelsemium elegans is widely and historically used to treat bone fracture and skin ulcers by the folk people of China. Two new monoterpenoid indole alkaloids, gelselegandines D and E, together with the known analogue gelegamine A were isolated from G. elegans. Their structures were elucidated by means of spectroscopic techniques and quantum chemical calculations. All isolated compounds were tested for the effects on RANKL-induced osteoclast formation. Interestingly, gelselegandine E and gelegamine A, respectively, showed significant promoting and inhibitory activities on osteoclastogenesis, while gelselegandine D had no activity under the same concentration. This work suggested the different configurations for the carbons near the C-19/20 oxygen rings of the isolated compounds may be the key active groups on osteoclast formation and provided the evidence for the rationality as the traditional treatment for bone-related diseases of G. elegans.
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页数:10
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