New Monoterpenoid Indoles with Osteoclast Activities from <i>Gelsemium elegans</i>
Xin Wei,
Rui Guo,
Xiao Wang,
Jia-Jun Liang,
Hao-Fei Yu,
Cai-Feng Ding,
Ting-Ting Feng,
Li-Yan Zhang,
Xia Liu,
Xin-Yue Hu,
Ying Zhou
Affiliations
Xin Wei
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Rui Guo
College of Chinese Materia Medica, Yunnan University of Chinese Medicine, Kunming 650500, China
Xiao Wang
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Jia-Jun Liang
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Hao-Fei Yu
Department of Zoology & Yunnan Key Laboratory of Pharmacology for Natural Products, School of Pharmaceutical Sciences, Kunming Medical University, Kunming 650500, China
Cai-Feng Ding
Department of Zoology & Yunnan Key Laboratory of Pharmacology for Natural Products, School of Pharmaceutical Sciences, Kunming Medical University, Kunming 650500, China
Ting-Ting Feng
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Li-Yan Zhang
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Xia Liu
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Xin-Yue Hu
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
Ying Zhou
School of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China
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.