Abstract
A series of novel 5-methyl-2,4-disubstitued-oxazole derivatives were synthesized and evaluated for their antitumor activities. The bioassay tests showed that 7-(5-methyl-2-(4-(R)phenyl)oxazol-4-yl)quinoline (R = trifluoromethyl, 2a; fluoro, 2b; chloro) and 2-(5-methyl-2-(4-(trifluoromethyl or fluoro)phenyl)oxazol-4-yl)pyrazine derivatives (4a and 4b) were highly effective against PC-3 cell with the IC50 values ranging from 1.2 to 2.0 μg/mL. 2-(2-(2,4-dichlorophenyl or 2,4-difluoro phenyl)-5-methyloxazol-4-yl)pyrazine (4e and 4f) were highly effective against A431 cell. The IC50 values of 4e and 4f against A431 cell were 2.0 and 1.6 μg/mL, respectively.
Keywords: Oxazole, Quoline, Synthese, Pyrazine, Antitumor activity
Letters in Drug Design & Discovery
Title: Novel 5-Methyl-2,4-Disubstitued-Oxazole Derivatives: Synthesis and Anticancer Activity
Volume: 7 Issue: 4
Author(s): Xin-Hua Liu, Hui-Feng Liu, Chun-Xiou Pan, Jin-Xin Li, Lin-Shan bai, Bao-An Song and Xiang-Feng Chu
Affiliation:
Keywords: Oxazole, Quoline, Synthese, Pyrazine, Antitumor activity
Abstract: A series of novel 5-methyl-2,4-disubstitued-oxazole derivatives were synthesized and evaluated for their antitumor activities. The bioassay tests showed that 7-(5-methyl-2-(4-(R)phenyl)oxazol-4-yl)quinoline (R = trifluoromethyl, 2a; fluoro, 2b; chloro) and 2-(5-methyl-2-(4-(trifluoromethyl or fluoro)phenyl)oxazol-4-yl)pyrazine derivatives (4a and 4b) were highly effective against PC-3 cell with the IC50 values ranging from 1.2 to 2.0 μg/mL. 2-(2-(2,4-dichlorophenyl or 2,4-difluoro phenyl)-5-methyloxazol-4-yl)pyrazine (4e and 4f) were highly effective against A431 cell. The IC50 values of 4e and 4f against A431 cell were 2.0 and 1.6 μg/mL, respectively.
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Cite this article as:
Liu Xin-Hua, Liu Hui-Feng, Pan Chun-Xiou, Li Jin-Xin, bai Lin-Shan, Song Bao-An and Chu Xiang-Feng, Novel 5-Methyl-2,4-Disubstitued-Oxazole Derivatives: Synthesis and Anticancer Activity, Letters in Drug Design & Discovery 2010; 7 (4) . https://dx.doi.org/10.2174/157018010790945878
DOI https://dx.doi.org/10.2174/157018010790945878 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
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