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New Monoterpenoid Indoles with Osteoclast Activities from Gelsemium elegans

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 stru...

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Detalles Bibliográficos
Autores principales: Wei, Xin, Guo, Rui, Wang, Xiao, Liang, Jia-Jun, Yu, Hao-Fei, Ding, Cai-Feng, Feng, Ting-Ting, Zhang, Li-Yan, Liu, Xia, Hu, Xin-Yue, Zhou, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708120/
https://www.ncbi.nlm.nih.gov/pubmed/34946539
http://dx.doi.org/10.3390/molecules26247457
Descripción
Sumario: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.