Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Novel 5-(3-(Substituted)-4,5-dihydroisoxazol-5-yl)-2-methoxyphenyl Derivatives: Synthesis and Anticancer Activity

Xin-Hua Liu A D , Bao-An Song C , Pinaki S. Bhadury C , Hai-Liang Zhu A B , Ping Cui A , Ke-Ke Hou C and Hong-Li Xu A
+ Author Affiliations
- Author Affiliations

A Key Laboratory of Anhui Educational Department, Anhui University of Technology, Maanshan, 243002, China.

B State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, 210093, China.

C Key Laboratory of Green Pesticide and Agriculture Bioengineering, Ministry of Education, Guizhou University, Guiyang, 55002, China.

D Corresponding author. Email: zlp@ahut.edu.cn

Australian Journal of Chemistry 61(11) 864-869 https://doi.org/10.1071/CH07395
Submitted: 16 November 2007  Accepted: 16 April 2008   Published: 5 November 2008

Abstract

Thirty novel 5-(3-(substituted phenyl)-4,5-dihydroisoxazol-5-yl)-2-methoxyphenyl derivatives were synthesized and evaluated for their antitumour activity. The bioassays showed that the 2-fluorobenzoyl derivative 6ai, the 4-trifluoromethylbenzoyl derivative 6ah, and the 3-trifluoromethyl isoxazole derivatives (6ch and 6ci) were highly effective against PC-3 cells. The IC50 values of 6ah and 6ai against PC-3 cells were 1.5 and 1.8 μg mL–1, respectively.


Acknowledgements

The authors thank the Anhui Natural Science Foundation, Anhui Province (Grant no. 070416274X) for providing financial support for the project and to thank the Student Research Train Project of Anhui Technology University (no. 08021). The work was also supported by the opening foundation of the Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, grant no. 2008GDGP0105.


References


[1]   V. S. Parmar, N. K. Sharma, M. Husain, A. C. Watterson, J. Kumar, L. A. Samuelson, A. L. Cholli, A. K. Prasad, A. Kumar, S. Malhotra, N. Kumar, A. Jha, A. Singh, I. Singh, Himanshu, A. Vats, N. A. Shakil, S. Trikha, S. Mukherjee, S. K. Sharma, S. K. Singh, A. Kumar, H. N. Jha, C. E. Olsen, C. P Stove, M. E. Bracke, M. M. Mareel, Bioorg. Med. Chem. 2003, 11,  913.
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
         
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  open url image1