
Synthesis and biological activities of novel 2-amino-1,3-thiazole-4-carboxylic acid derivatives
English
Synthesis and biological activities of novel 2-amino-1,3-thiazole-4-carboxylic acid derivatives
-
Key words:
- 1,3-Thiazole derivatives
- / Fungicidal activity
- / Anti-TMV activity
-
-
-
[1] Z.J. Fan, X.F. Liu, F.L. Liu, L.L. Bao, Y.G. Zhang, Progress of researches on induced resistance of plant activator, Acta Phytophy. Sin. 32(2005) 87-92.[1] Z.J. Fan, X.F. Liu, F.L. Liu, L.L. Bao, Y.G. Zhang, Progress of researches on induced resistance of plant activator, Acta Phytophy. Sin. 32(2005) 87-92.
-
[2] Z.J. Fan, Z.G. Shi, H.K. Zhang, et al., Synthesis and biological activity evaluation of 1,2,3-thiadiazole derivatives as potential elicitors with highly systemic acquired resistance, J. Agric. Food Chem. 57(2009) 4279-4286.[2] Z.J. Fan, Z.G. Shi, H.K. Zhang, et al., Synthesis and biological activity evaluation of 1,2,3-thiadiazole derivatives as potential elicitors with highly systemic acquired resistance, J. Agric. Food Chem. 57(2009) 4279-4286.
-
[3] C.L. Liu, L. Li, Z.M. Li, Design, synthesis, and biological activity of novel 4-(3, 4-dimethoxyphenyl)-2-methylthiazole-5-carboxylic acid derivatives, Bioorg. Med. Chem. 12(2004) 2825-2830.[3] C.L. Liu, L. Li, Z.M. Li, Design, synthesis, and biological activity of novel 4-(3, 4-dimethoxyphenyl)-2-methylthiazole-5-carboxylic acid derivatives, Bioorg. Med. Chem. 12(2004) 2825-2830.
-
[4] A.R. Jalilian, S. Sattari, M. Bineshmarvasti, A. Shafiee, M. Daneshtalab, Synthesis and in vitro antifungal and cytotoxicity evaluation of thiazolo-4H-1,2,4-triazoles and 1,2,3-thiadiazolo-4H-1,2,4-triazoles, Arch. Pharm. Med. Chem. 333(2000) 347-354.[4] A.R. Jalilian, S. Sattari, M. Bineshmarvasti, A. Shafiee, M. Daneshtalab, Synthesis and in vitro antifungal and cytotoxicity evaluation of thiazolo-4H-1,2,4-triazoles and 1,2,3-thiadiazolo-4H-1,2,4-triazoles, Arch. Pharm. Med. Chem. 333(2000) 347-354.
-
[5] S. Vengurlekar, S. Prachand, S. Jain, R. Gupta, Synthesis and evaluation of some thiazole derivatives as an antifungal agent, Int. J. Pharm. Life Sci. 5(2014) 3526-3530.[5] S. Vengurlekar, S. Prachand, S. Jain, R. Gupta, Synthesis and evaluation of some thiazole derivatives as an antifungal agent, Int. J. Pharm. Life Sci. 5(2014) 3526-3530.
-
[6] T.T. Wang, G.F. Bing, X. Zhang, et al., Synthesis and herbicidal activities of 2-cyano-3-benzylaminoacrylates containing thiazole moiety, Bioorg. Med. Chem. Lett. 20(2010) 3348-3351.[6] T.T. Wang, G.F. Bing, X. Zhang, et al., Synthesis and herbicidal activities of 2-cyano-3-benzylaminoacrylates containing thiazole moiety, Bioorg. Med. Chem. Lett. 20(2010) 3348-3351.
-
[7] H. Dai, Y.S. Xiao, Z. Li, X.Y. Xu, X.H. Qian, The thiazoylmethoxy modification on pyrazole oximes:synthesis and insecticidal biological evaluation beyond acaricidal activity, Chin. Chem. Lett. 25(2014) 1014-1016.[7] H. Dai, Y.S. Xiao, Z. Li, X.Y. Xu, X.H. Qian, The thiazoylmethoxy modification on pyrazole oximes:synthesis and insecticidal biological evaluation beyond acaricidal activity, Chin. Chem. Lett. 25(2014) 1014-1016.
-
[8] X. Qin, H.B. Yu, H. Dai, et al., Synthesis and plant-growth regulatory activities of novel imine derivatives containing 1H-1,2,4-triazole and thiazole rings, Chin. Chem. Lett. 21(2010) 283-286.[8] X. Qin, H.B. Yu, H. Dai, et al., Synthesis and plant-growth regulatory activities of novel imine derivatives containing 1H-1,2,4-triazole and thiazole rings, Chin. Chem. Lett. 21(2010) 283-286.
-
[9] H.B. Yu, L. Shao, J.X. Fang, Synthesis and biological activity research of novel ferrocenyl-containing thiazole imine derivatives, J. Organomet. Chem. 692(2007) 991-996.[9] H.B. Yu, L. Shao, J.X. Fang, Synthesis and biological activity research of novel ferrocenyl-containing thiazole imine derivatives, J. Organomet. Chem. 692(2007) 991-996.
-
[10] A.S. Mayhoub, M. Khaliq, C. Botting, et al., An investigation of phenylthiazole antiflaviviral agents, Bioorg. Med. Chem. 19(2011) 3845-3854.[10] A.S. Mayhoub, M. Khaliq, C. Botting, et al., An investigation of phenylthiazole antiflaviviral agents, Bioorg. Med. Chem. 19(2011) 3845-3854.
-
[11] P. Maienfisch, M. Angst, F. Brandl, et al., Chemistry and biology of thiamethoxam:a second generation neonicotinoid, Pest Manag. Sci. 57(2001) 906-913.[11] P. Maienfisch, M. Angst, F. Brandl, et al., Chemistry and biology of thiamethoxam:a second generation neonicotinoid, Pest Manag. Sci. 57(2001) 906-913.
-
[12] M.H. Lee, S.M. Pan, T.W. Ng, et al., Mutations of β-tubulin codon 198 or 200 indicate thiabendazole resistance among isolates of Penicillium digitatum collected from citrus in Taiwan, Int. J. Food Microbiol. 150(2011) 157-163.[12] M.H. Lee, S.M. Pan, T.W. Ng, et al., Mutations of β-tubulin codon 198 or 200 indicate thiabendazole resistance among isolates of Penicillium digitatum collected from citrus in Taiwan, Int. J. Food Microbiol. 150(2011) 157-163.
-
[13] H.C. Feng, Novel fungicide benthiavalicarbisopropyl, World Pestic. 30(2008) 51.[13] H.C. Feng, Novel fungicide benthiavalicarbisopropyl, World Pestic. 30(2008) 51.
-
[14] J. Huang, D. Wu, H.J. Ge, S.H. Liu, J. Yin, Fluorinated 1,8-naphthalimides:synthesis, solid structure and properties, Chin. Chem. Lett. 25(2014) 1399-1402.[14] J. Huang, D. Wu, H.J. Ge, S.H. Liu, J. Yin, Fluorinated 1,8-naphthalimides:synthesis, solid structure and properties, Chin. Chem. Lett. 25(2014) 1399-1402.
-
[15] C.L. Liu, Z.M. Li, B. Zhang, synthesis and biological activity of novel 2-methyl-4-trifluoromethyl-thiazole-5-carboxamide derivatives, J. Fluorine Chem. 125(2004) 1287-1290.[15] C.L. Liu, Z.M. Li, B. Zhang, synthesis and biological activity of novel 2-methyl-4-trifluoromethyl-thiazole-5-carboxamide derivatives, J. Fluorine Chem. 125(2004) 1287-1290.
-
[16] Y.B. Chen, J.L. Li, X.S. Shao, X.Y. Xu, Z. Li, Design, synthesis and insecticidal activity of novel anthranilic diamides with benzyl sulfide scaffold, Chin. Chem. Lett. 24(2013) 673-676.[16] Y.B. Chen, J.L. Li, X.S. Shao, X.Y. Xu, Z. Li, Design, synthesis and insecticidal activity of novel anthranilic diamides with benzyl sulfide scaffold, Chin. Chem. Lett. 24(2013) 673-676.
-
[17] Z.Y. Yu, G.Y. Shi, Q. Sun, et al., Design, synthesis and in vitro antibacterial/antifungal evaluation of novel 1-ethyl-6-fluoro-1, 4-dihydro-4-oxo-7(1-piperazinyl) quinoline-3-carboxylic acid derivatives, Eur. J. Med. Chem. 44(2009) 4726-4733.[17] Z.Y. Yu, G.Y. Shi, Q. Sun, et al., Design, synthesis and in vitro antibacterial/antifungal evaluation of novel 1-ethyl-6-fluoro-1, 4-dihydro-4-oxo-7(1-piperazinyl) quinoline-3-carboxylic acid derivatives, Eur. J. Med. Chem. 44(2009) 4726-4733.
-
[18] C.B. Vicentini, C. Romagnoli, E. Andreotti, D. Mares, Synthetic pyrazole derivatives as growth inhibitors of some phytopathogenic fungi, J. Agric. Food Chem. 55(2007) 10331-10338.[18] C.B. Vicentini, C. Romagnoli, E. Andreotti, D. Mares, Synthetic pyrazole derivatives as growth inhibitors of some phytopathogenic fungi, J. Agric. Food Chem. 55(2007) 10331-10338.
-
[19] H. Cerecetto, E. Dias, R.D. Maio, et al., Synthesis and herbicidal activity of N-oxide derivatives, J. Agric. Food Chem. 48(2000) 2995-3002.[19] H. Cerecetto, E. Dias, R.D. Maio, et al., Synthesis and herbicidal activity of N-oxide derivatives, J. Agric. Food Chem. 48(2000) 2995-3002.
-
[20] V. Ehmke, J.E.Q. Quinsaat, P. Rivera-Fuentes, et al., Tuning and predicting biological affinity:aryl nitriles as cysteine protease inhibitors, Org. Biomol. Chem. 10(2012) 5764-5768.[20] V. Ehmke, J.E.Q. Quinsaat, P. Rivera-Fuentes, et al., Tuning and predicting biological affinity:aryl nitriles as cysteine protease inhibitors, Org. Biomol. Chem. 10(2012) 5764-5768.
-
[21] N.P. Belskaya, K.I. Lugovik, A.D. Ivina, V.A. Bakulev, Z.J. Fan, Reaction of enamines and azaenamines containing a thioamide group with dimethyl acetylenedicarboxylate, Chem. Heterocycl. Compd. 50(2014) 888-900.[21] N.P. Belskaya, K.I. Lugovik, A.D. Ivina, V.A. Bakulev, Z.J. Fan, Reaction of enamines and azaenamines containing a thioamide group with dimethyl acetylenedicarboxylate, Chem. Heterocycl. Compd. 50(2014) 888-900.
-
[22] Z.J. Fan, Z.K. Yang, H.K. Zhang, et al., Synthesis, crystal structure, and biological activity of 4-methyl-1,2,3-thiadiazole-containing 1,2,4-triazolo[3,4-b] [1,3,4] thiadiazoles, J. Agric. Food. Chem. 58(2010) 2630-2636.[22] Z.J. Fan, Z.K. Yang, H.K. Zhang, et al., Synthesis, crystal structure, and biological activity of 4-methyl-1,2,3-thiadiazole-containing 1,2,4-triazolo[3,4-b] [1,3,4] thiadiazoles, J. Agric. Food. Chem. 58(2010) 2630-2636.
-
[23] Y.D. Li, W.T. Mao, Z.J. Fan, et al., Synthesis and biological evaluation of novel 1,2, 4-triazole containing 1,2,3-thiadiazole derivatives, Chin. Chem. Lett. 24(2013) 1134-1136.[23] Y.D. Li, W.T. Mao, Z.J. Fan, et al., Synthesis and biological evaluation of novel 1,2, 4-triazole containing 1,2,3-thiadiazole derivatives, Chin. Chem. Lett. 24(2013) 1134-1136.
-
-

计量
- PDF下载量: 0
- 文章访问数: 1134
- HTML全文浏览量: 14