期刊文献+

Design, Synthesis, Antifungal Activities and SARs of (R)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acid Derivatives 被引量:2

Design, Synthesis, Antifungal Activities and SARs of (R)-2-Aryl-4,5-dihydrothiazole-4-carboxylic Acid Derivatives
原文传递
导出
摘要 Based on the structure of natural product 2-aryl-4,5-dihydrothiazole-4-carboxylic acid, a series of novel (R)-2-aryl-4,5-dihydrothiazole-4-carboxylic acid derivatives were designed and synthesized. Their structures were characterized by ^1H NMR, ^13C NMR and HRMS. The single crystal structure of compound 9b was determined by X-ray diffraction analysis. The antifungal activities were evaluated for the first time. The bioassay results indicated that most compounds exhibited moderate to good antifungal activities. The antifungal activities of compound 13a (against Cercospora arachidicola Hori), 13d (against Alternaria solani), and 16e (against Cercospora arachidieola Hori) were 61.9%, 67.3% and 61.9%, respectively, which are higher than those of the commercial fungicides chlorothalonil and carbendazim. Moreover, compound 13d exhibited excellent antifungal activities against 7 kinds of the fungi tested (66.7%, 77.3%, 63.0%, 87.9%, 70.0%, 70.0% and 80.0% at 50 μg/mL). Therefore, 13d can be used as a new lead structure for the development of antifungal agents. Based on the structure of natural product 2-aryl-4,5-dihydrothiazole-4-carboxylic acid, a series of novel (R)-2-aryl-4,5-dihydrothiazole-4-carboxylic acid derivatives were designed and synthesized. Their structures were characterized by ^1H NMR, ^13C NMR and HRMS. The single crystal structure of compound 9b was determined by X-ray diffraction analysis. The antifungal activities were evaluated for the first time. The bioassay results indicated that most compounds exhibited moderate to good antifungal activities. The antifungal activities of compound 13a (against Cercospora arachidicola Hori), 13d (against Alternaria solani), and 16e (against Cercospora arachidieola Hori) were 61.9%, 67.3% and 61.9%, respectively, which are higher than those of the commercial fungicides chlorothalonil and carbendazim. Moreover, compound 13d exhibited excellent antifungal activities against 7 kinds of the fungi tested (66.7%, 77.3%, 63.0%, 87.9%, 70.0%, 70.0% and 80.0% at 50 μg/mL). Therefore, 13d can be used as a new lead structure for the development of antifungal agents.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2015年第11期1269-1275,共7页 中国化学(英文版)
基金 We gratefully acknowledge the financial support of this work by the "111" Project of Ministry of Education of China (No. B06005) and the Natural Science Foundation of China (No. 31370039).
关键词 (R)-2-aryl-4 5-dihydrothiazole-4-carboxylic acid SYNTHESIS antifungal activity structure-activity relationship (R)-2-aryl-4,5-dihydrothiazole-4-carboxylic acid, synthesis, antifungal activity, structure-activity relationship
  • 相关文献

参考文献32

  • 1Zhang, H.; Liu, K. C.; Liu, R. Q.; Li, Q. B.; Li, Y. Q.; Wang, Q. M.; Liu, S. Z. Chin. J. Chem. 2015, 33, 749.
  • 2Zhou, H.; Duan, Z. G; Zhao, S.; Bao, M. Y.; Li, Z. W.; Pei, Y. Z. Chem. J. Chin. Univ. 2015, 36, 1694 (in Chinese).
  • 3Ino, A.; Hasegawa, Y.; Murabayashi, A. Tetrahedron Lett. 1998, 39, 3509.
  • 4Bergeron, R. J.; Wiegand, J.; McManis, J. S.; McCosar, B. H.; Weimar, W. R.; Brittenham, G. M.; Smith, R. E. J. Med. Chem. 1999, 42, 2432.
  • 5Li, W.; Lu, Y.; Wang, Z.; Dalton, J. T.; Miller, D. D. Bioorg. Med. Chem. Lett. 2007, 77, 4113.
  • 6Li, W.; Wang, Z.; Gududuru, V.; Zbytek, B.; Slominski, A. T.; Dalton, J. T.; Miller, D. D. Anticancer Res. 2007, 27, 883.
  • 7Pattenden, G.; Thom, S. T. J. Chem. Soc., Perkin Trans 1 1993, 1629.
  • 8Mao, J.; Chen, J. Y.; Li, R. X.; Wang, H. Y.; Li, J.; Han, J. X. Chin. J. Appl. Chem. 2004, 21, 1265 (in Chinese).
  • 9Zheng, Z. B.; Sun, Y. J.; Liu, L.; Yu, Y. B.; Yuan, H. J.; Fu, B. Modern Agrochemicals 2009, 8, 8 (in Chinese).
  • 10Liu, L.; Zheng, Z. B.; Qin, Z. H.; Fu, B.; Yuan, H. Z. Chin. J. Org. Chem. 2008, 28, 1841 (in Chinese).

同被引文献9

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部