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Molecules 2011, 16(6), 4897-4911; doi:10.3390/molecules16064897
Article

Synthesis and In Vitro Protein Tyrosine Kinase Inhibitory Activity of Furan-2-yl(phenyl)methanone Derivatives

1, 1, 1, 1, 2 and 1,2,*
Received: 27 April 2011; in revised form: 1 June 2011 / Accepted: 7 June 2011 / Published: 14 June 2011
(This article belongs to the Section Medicinal Chemistry)
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Abstract: A series of novel furan-2-yl(phenyl)methanone derivatives were synthesized, and their structures were established on the basis of 1H-NMR, 13C-NMR and mass spectral data. All the prepared compounds were screened for their in vitro protein tyrosine kinase inhibitory activity and several new derivatives exhibited promising activity, which, in some cases, was identical to, or even better than that of genistein, a positive reference compound. The preliminary structure-activity relationships of these compounds were investigated and are discussed.
Keywords: halophenols; furan-2-yl(phenyl)methanone; protein tyrosine kinases inhibitor; structure-activity relationships (SAR) halophenols; furan-2-yl(phenyl)methanone; protein tyrosine kinases inhibitor; structure-activity relationships (SAR)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Zheng, F.L.; Ban, S.R.; Feng, X.E.; Zhao, C.X.; Lin, W.; Li, Q.S. Synthesis and In Vitro Protein Tyrosine Kinase Inhibitory Activity of Furan-2-yl(phenyl)methanone Derivatives. Molecules 2011, 16, 4897-4911.

AMA Style

Zheng FL, Ban SR, Feng XE, Zhao CX, Lin W, Li QS. Synthesis and In Vitro Protein Tyrosine Kinase Inhibitory Activity of Furan-2-yl(phenyl)methanone Derivatives. Molecules. 2011; 16(6):4897-4911.

Chicago/Turabian Style

Zheng, Fei Lang; Ban, Shu Rong; Feng, Xiu E; Zhao, Cheng Xiao; Lin, Wenhan; Li, Qing Shan. 2011. "Synthesis and In Vitro Protein Tyrosine Kinase Inhibitory Activity of Furan-2-yl(phenyl)methanone Derivatives." Molecules 16, no. 6: 4897-4911.


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