906481-17-2Relevant academic research and scientific papers
Synthesis and biological evaluation of 2,3-diarylthiophene analogues of combretastatin A-4
Wang, Zhan,Yang, Qingkun,Bai, Zhaoshi,Sun, Jun,Jiang, Xuewei,Song, Hongrui,Wu, Yingliang,Zhang, Weige
, p. 971 - 976 (2015/05/27)
A series of novel 2,3-diarylthiophene analogues of combretastatin A-4 (CA-4) were designed with a rigid thiophene moiety to retain the cis-olefin configuration of CA-4 and were subsequently synthesised. All of the target compounds were evaluated for their
Synthesis and biological evaluation of novel 3,4-diaryl-1,2,5-selenadiazol analogues of combretastatin A-4
Guan, Qi,Yang, Fushan,Guo, Dandan,Xu, Jingwen,Jiang, Mingyang,Liu, Chunjiang,Bao, Kai,Wu, Yingliang,Zhang, Weige
, p. 1 - 9 (2015/02/05)
A set of novel selenium-containing heterocyclic analogues of combretastatin A-4 (CA-4) have been designed and synthesised using a rigid 1,2,5-selenadiazole as a linker to fix the cis-orientation of ring-A and ring-B. All of the target compounds were evalu
COMPOUNDS FOR THE TREATMENT OF ANGIOGENESIS
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Page/Page column 296-297, (2008/06/13)
The invention relates to isoxazole, isothiazole, and triazole compounds that are useful for treating or inhibiting angiogenesis.
Synthesis and activity of Combretastatin A-4 analogues: 1,2,3-thiadiazoles as potent antitumor agents
Wu, Maojiang,Sun, Qiming,Yang, Chunhao,Chen, Dongdong,Ding, Jian,Chen, Yi,Lin, Liping,Xie, Yuyuan
, p. 869 - 873 (2007/10/03)
A series of 4,5-disubstitute-1,2,3-thiadiazole compounds were designed and synthesized as potent anticancer agents, some of them exhibited excellent in vitro and in vivo inhibitory activity.
Synthesis and cytotoxic activities of 4,5-diarylisoxazoles
Sun, Chang-Ming,Lin, Lee-Gin,Yu, Hsi-Jung,Cheng, Chih-Yu,Tsai, Ya-Chuan,Chu, Chi-Wei,Din, Yi-Hui,Chau, Yat-Pang,Don, Ming-Jaw
, p. 1078 - 1081 (2007/10/03)
A series of 4,5-diarylisoxazoles related to combretastatin A-4 (CA-4) were synthesized and evaluated for cytotoxicity against three human cancer cell lines. Among them, compound 6e showed better cytotoxic activity than CA-4 in HeLa and HepG2 cell lines as
COMPOUNDS FOR THE TREATMENT OF PROLIFERATIVE DISORDERS
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Page/Page column 221, (2008/06/13)
The invention relates to compounds of structural formula (I); or a pharmaceutically acceptable salt, solvate, clathrate, and prodrug thereof, wherein Ra, Rb, and R2 are defined herein. These compounds inhibit tubulin polym
