Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Fa-Wu Dong"'
Autor:
Ting Li, Qiu-ping Zou, Feng Huang, Gui-guang Cheng, Ze-wei Mao, Ting Wang, Fa-wu Dong, Bao-jing Li, Hong-ping He, Yan-ping Li
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 24, Iss 5, Pp 595-603 (2021)
Objective(s): This study aimed to find out the protective effects and preliminary mechanisms of the flower extract of Caragana sinica (FEC) on dextran sulfate sodium salt (DSS)-induced colitis.Materials and Methods: The ulcerative colitis models of m
Externí odkaz:
https://doaj.org/article/f283c4638a304df695fd686894df458f
Autor:
Cheng-Ting Zi, Ying-Sheng Gao, Liu Yang, Shu-Yun Feng, Yue Huang, Li Sun, Yi Jin, Feng-Qing Xu, Fa-Wu Dong, Yan Li, Zhong-Tao Ding, Jun Zhou, Zi-Hua Jiang, Sheng-Tao Yuan, Jiang-Miao Hu
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
Podophyllotoxin has long been used as an active substance for cytotoxic activity. Fourteen novel biotinylated podophyllotoxin derivatives were designed, synthesized, and evaluated for cytotoxic activity for this study. The synthesized compounds were
Externí odkaz:
https://doaj.org/article/42c648a234c34b5481d840b4ad5af963
Autor:
Fa-Wu Dong, He-Hai Jiang, Liu Yang, Ye Gong, Cheng-Ting Zi, Dan Yang, Chen-Jun Ye, Huan Li, Jian Yang, Yin Nian, Jun Zhou, Jiang-Miao Hu
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
The roots and rhizomes of Valeriana jatamansi have long been used as folk medicine in Asia and usually named as “Zhizhuxiang” in Chinese for the treatment of abdominal distention and pain. However, its active ingredients and molecular targets for
Externí odkaz:
https://doaj.org/article/5d7a6c4cd7044e808dbdbbe656099b08
Publikováno v:
Chinese Journal of Natural Medicines. 17:900-905
Three new sesquiterpene glycosides with alloaromadendrane and ylangene-derived type aglycones, named dendrofindlayanosides A-C (1-3), one new cyclopacamphane type sesquiterpene named dendrofindlayanobilin A (4), together with five known compounds hav
Autor:
Shi-Li, Wu, Qiu-Ping, Zou, Xiao-Yan, Xie, Jia-Jia, Ren, Zhang, Fan, Jing-Rong, OuYang, Peng-Cheng, Yin, Fa-Wu, Dong, Hong-Ping, He
Publikováno v:
Journal of Asian natural products research. 24(8)
Two new triucallane triterpenoids, polystanin F (
Autor:
Ting, Li, Qiu-Ping, Zou, Feng, Huang, Gui-Guang, Cheng, Ze-Wei, Mao, Ting, Wang, Fa-Wu, Dong, Bao-Jing, Li, Hong-Ping, He, Yan-Ping, Li
Publikováno v:
Iranian Journal of Basic Medical Sciences
Objective(s): This study aimed to find out the protective effects and preliminary mechanisms of the flower extract of Caragana sinica (FEC) on dextran sulfate sodium salt (DSS)-induced colitis. Materials and Methods: The ulcerative colitis models of
Autor:
Dan Yang, Bo Hou, Jiang-Miao Hu, Liu Yang, Fa-Wu Dong, Cheng-Ting Zi, Jun Zhou, Zhong-Quan Cheng
Publikováno v:
Fitoterapia. 144
Two unusual dendrobine-type alkaloids, findlayines E and F (1, 2), along with five known dendrobine-type alkaloids (3-7), were isolated from the stems of Dendrobium findlayanum Par. et Rchb. f. Compound 1 is the first example of dendrobine-type alkal
Autor:
Liu Yang, Zheng-Hua Liu, Cheng-Ting Zi, Jiang-Miao Hu, Zhong-Tao Ding, Jun Zhou, Zhong-Quan Cheng, Jing Yang, Xiao-Nian Li, Bo Hou, Dan Yang, Fa-Wu Dong
Publikováno v:
Journal of Natural Products. 81:227-235
Investigation of the 95% EtOH extract of stems of Dendrobium findlayanum afforded four new seco-dendrobines, findlayines A–D (1–4); two known dendrobines, dendrobine (5) and 2-hydroxydendrobine (6); and four new phenolic compounds, dendrofindlaph
Autor:
Feng-Qing Xu, Zhong-Quan Cheng, Fa-Wu Dong, Dan Yang, Weiwei Fan, Xiao-Yong Wei, Jiang-Miao Hu
Publikováno v:
Phytochemistry. 190:112858
Ten undescribed picrotoxane-type sesquiterpenoids, dendrowardins A–J, together with two known ones, were isolated from the stems of Dendrobium wardianum Warner (Orchidaceae). Dendrowardins A–D feature the unusual 5,2-δ-lactone and additionally d
Publikováno v:
RSC Adv.. 7:45878-45884
In China, the roots and rhizomes of Valeriana jatamansi Jones are traditionally used to treat gastrointestinal and rheumatic pain. Small molecule inhibitors of N-type (Cav2.2) and T-type (Cav3.1–3.3) calcium channels have become attractive resource