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- Recognition of α-amino acid derivatives by N,N′-dibenzylated S,S-(+)-tetrandrine. Karen Ochoa Lara, Carolina Godoy-Alcántar, Alexey V. Eliseev, Anatoly K. Yatsimirsky
, Org. Biomol. Chem.
, 2004
, 2
, 1712
- The biology and total syntheses of bisbenzylisoquinoline alkaloids. Viviene K. Nguyen, Kevin. G. M. Kou
, Org. Biomol. Chem.
, 2021
, 19
, 7535
- Development of a new tetrandrine certified reference material for clinical chemistry and pharmaceutical analysis. Dezhi Yang, Fengfeng Wang, Li Zhang, Yang Lv
, Anal. Methods
, 2015
, 7
, 4763
- A modular approach to the bisbenzylisoquinoline alkaloids tetrandrine and isotetrandrine. Ramona Schütz, Maximilian Meixner, Iris Antes, Franz Bracher
, Org. Biomol. Chem.
, 2020
, 18
, 3047
- The luminescence of bisbenzyltetrahydroisoquinoline alkaloids. The berbamine and oxyacanthine alkaloids. Ernest P. Gibson, James H. Turnbull
, J. Chem. Soc., Perkin Trans. 2
, 1980
, 1696
- Design, synthesis and bioactivity investigation of tetrandrine derivatives as potential anti-cancer agents. Junrong Song, Junjie Lan, Chao Chen, Shengcao Hu, Jialei Song, Wulin Liu, Xueyi Zeng, Huayong Lou, Yaacov Ben-David, Weidong Pan
, Med. Chem. Commun.
, 2018
, 9
, 1131
- Studies on the alkaloids of menispermaceous plants. Part CCXLIX. Total synthesis of optically active natural isotetrandrine, phaeanthine, and tetrandrine. Yasuo Inubushi, Yukio Masaki, Saichi Matsumoto, Fumitaka Takami
, J. Chem. Soc. C
, 1969
, 1547
- Pharmacokinetic/pharmacodynamic modelling of effective components of Fangji Huangqi Tang for its treatment of nephrotic syndrome. Xiao Liu, Xiaochai Zhu, Li Xie, Baochang Cai
, New J. Chem.
, 2019
, 43
, 338
- Fluorescent and colorimetric chemosensors for detection of nucleotides, FAD and NADH: highlighted research during 2004–2010. Ying Zhou, Zhaochao Xu, Juyoung Yoon
, Chem. Soc. Rev.
, 2011
, 40
, 2222
- Synthesis, crystal structures and phase transformation of the new solid-state forms of tetrandrine. Zhengzheng Zhou, Henry H. Y. Tong, Liang Li, Fanny L. Y. Shek, Yang Lv, Ying Zheng
, RSC Adv.
, 2014
, 4
, 62586