Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Fang-Ru Li"'
Discovery and biosynthesis of bacterial drimane-type sesquiterpenoids from Streptomyces clavuligerus
Autor:
Dongxu Zhang, Wenyu Du, Xingming Pan, Xiaoxu Lin, Fang-Ru Li, Qingling Wang, Qian Yang, Hui-Min Xu, Liao-Bin Dong
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 815-822 (2024)
Drimane-type sesquiterpenoids (DMTs) are characterized by a distinctive 6/6 bicyclic skeleton comprising the A and B rings. While DMTs are commonly found in fungi and plants, their presence in bacteria has not been reported. Moreover, the biosyntheti
Externí odkaz:
https://doaj.org/article/b3b62f2db2c2461b938c840da06a8a8e
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 881-888 (2022)
The clerodane and ent-kaurane diterpenoids are two typical categories of diterpenoid natural products with complicated polycyclic carbon skeletons and significant pharmacological activities. Despite exciting advances in organic chemistry, access to t
Externí odkaz:
https://doaj.org/article/9043803c93e24926977620aaab7c1e2f
Autor:
Fang-ru Li, 李方儒
92
We examined 1) ambush site characteristics, 2) orientations and posture of ambushing snakes and 3) the correlation between abiotic factors, preys and snakes to study the ambush site selection by the sit-and-wait pit-viper, Trimeresurus s. ste
We examined 1) ambush site characteristics, 2) orientations and posture of ambushing snakes and 3) the correlation between abiotic factors, preys and snakes to study the ambush site selection by the sit-and-wait pit-viper, Trimeresurus s. ste
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/30402240734947443484
Autor:
Si-Fan Teng, Fang-Ru Li, Qi-Min Cui, Afsar Khan, Ting He, Xiao-Dong Luo, Ya-Ping Liu, Gui-Guang Cheng
Publikováno v:
Phytochemistry Reviews.
Autor:
Xingming Pan, Wenyu Du, Xiaowei Zhang, Xiaoxu Lin, Fang-Ru Li, Qian Yang, Hang Wang, Jeffrey D. Rudolf, Bo Zhang, Liao-Bin Dong
Terpene cyclases (TCs), the extraordinary enzymes that create the structural diversity seen in terpene natural products, are traditionally divided into two classes. Although the structural and mechanistic features in class I TCs are well-known, the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458601d802fe4549666f8b8e4eda8c79
https://doi.org/10.26434/chemrxiv-2022-xxfqd
https://doi.org/10.26434/chemrxiv-2022-xxfqd
Publikováno v:
Records of Natural Products. 14:387-394
Autor:
Fang-Ru Li, Afsar Khan, Gui-Guang Cheng, Jianxin Cao, Li-Wen Liang, Tianrui Zhao, Lu Liu, Jin-Tang Wang
Publikováno v:
Biochemical Systematics and Ecology. 84:71-74
Phytochemical investigation on the aerial parts of Melodinus hemsleyanus diels (Jahrb, Syst, 1995) led to the isolation and identification of 27 compounds, including fifteen aspidosperma-type alkaloids (1–15), four quinoline-type alkaloids (16–19
Autor:
Xu-Jie Qin, Yudan Wang, Meilian Yang, Afsar Khan, Yaping Liu, Lu Liu, Gui-Guang Cheng, Fang-Ru Li, Jin-Tang Wang
Publikováno v:
Phytochemistry. 184
The Melodinus species have been proved to be good resources of bisindole alkaloids. Six bisindole alkaloids were isolated from the leaves and stems of Melodinus cochinchinensis (Lour.) Merr. guided by HRESIMS data analysis. Among them, melokhanines K
Autor:
Jianxin Cao, Jian Fan, Fang-Ru Li, Qian Shengyan, Jin-Tang Wang, Tianrui Zhao, Afsar Khan, Gui-Guang Cheng
Publikováno v:
Biochemical Systematics and Ecology. 79:50-53
Phytochemical investigation on the aerial parts of Trachelospermum dunnii led to the isolation and identification of 16 compounds, including nine dibenzylbutyrolactone lignans ( 1 – 9 ), two furanoid lignans ( 10 – 11 ), one dihydrobenzofuran lig
Autor:
Yudan Wang, Fang-Ru Li, Ya-Ping Liu, Qimin Cui, Tianrui Zhao, Shuyue He, Gui-Guang Cheng, Ting He
Publikováno v:
Biochemical Systematics and Ecology. 93:104159
A phytochemical investigation on the twigs and leaves of Kopsia hainanensis Tsiang resulted in the isolation and identification of 18 alkaloids, including two sarpagine type alkaloids (1 and 2), five eburnane type alkaloids (3–7), three aspidofract