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Volumn 6, Issue 1, 2012, Pages

Synthesis and antifungal activity of novel pyrazolecarboxamide derivatives containing a hydrazone moiety

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EID: 84861565683     PISSN: None     EISSN: 1752153X     Source Type: Journal    
DOI: 10.1186/1752-153X-6-51     Document Type: Article
Times cited : (34)

References (23)
  • 1
    • 4744352786 scopus 로고    scopus 로고
    • Management and resistance in wheat and barley to fusarium head blight
    • 10.1146/annurev.phyto.42.040803.140340, 15283663
    • Bai GH, Gregory S. Management and resistance in wheat and barley to fusarium head blight. Annu Rev Phytopathol 2004, 42:135-161. 10.1146/annurev.phyto.42.040803.140340, 15283663.
    • (2004) Annu Rev Phytopathol , vol.42 , pp. 135-161
    • Bai, G.H.1    Gregory, S.2
  • 2
    • 0037377371 scopus 로고    scopus 로고
    • Risk assessment models for wheat Fusarium head blight epidemics based on within-season weather data
    • De Wolf ED, Madden LV, Lipps PE. Risk assessment models for wheat Fusarium head blight epidemics based on within-season weather data. Phytopathol. 2003, 93:428-435.
    • (2003) Phytopathol. , vol.93 , pp. 428-435
    • De Wolf, E.D.1    Madden, L.V.2    Lipps, P.E.3
  • 3
    • 0008557641 scopus 로고
    • Synthesis and herbicidal activity of 1-aryl-5-halo-and 1-aryl-5-(trifluoromethyl)-1 H-pyrazole-4-carboxamides
    • Thomas WW, James RB, Michael PL, Fred LW. Synthesis and herbicidal activity of 1-aryl-5-halo-and 1-aryl-5-(trifluoromethyl)-1 H-pyrazole-4-carboxamides. J Agric Food Chem 1990, 38:541-544.
    • (1990) J Agric Food Chem , vol.38 , pp. 541-544
    • Thomas, W.W.1    James, R.B.2    Michael, P.L.3    Fred, L.W.4
  • 4
    • 84856733643 scopus 로고    scopus 로고
    • Synthesis and fungicidal activity of pyrazolecarboxamide containing α-aminoacetanilide Moiety
    • Fang ZY, Jiang H, Ye XD. Synthesis and fungicidal activity of pyrazolecarboxamide containing α-aminoacetanilide Moiety. E-J. Chem 2012, 9:211-218.
    • (2012) E-J. Chem , vol.9 , pp. 211-218
    • Fang, Z.Y.1    Jiang, H.2    Ye, X.D.3
  • 5
    • 78349249491 scopus 로고    scopus 로고
    • Design, synthesis and insecticidal evaluation of novel pyrazolecarboxamides containing cyano substituted N-pyridylpyrazole
    • Liu ZL, Feng Q, Xiong LX, Wang MZ, Li ZM. Design, synthesis and insecticidal evaluation of novel pyrazolecarboxamides containing cyano substituted N-pyridylpyrazole. Chin J. Chem. 2010, 28:1757-1760.
    • (2010) Chin J. Chem. , vol.28 , pp. 1757-1760
    • Liu, Z.L.1    Feng, Q.2    Xiong, L.X.3    Wang, M.Z.4    Li, Z.M.5
  • 6
    • 55249098392 scopus 로고    scopus 로고
    • Synthesis of new fluorinated tebufenpyrad analogs with acaricidal activity through regioselective pyrazole formation
    • 10.1021/jo801729p, 18855479
    • Fustero S, Román R, Sanz-Cervera JF, Simón-Fuentes A, Bueno J, Villanova S. Synthesis of new fluorinated tebufenpyrad analogs with acaricidal activity through regioselective pyrazole formation. J Org Chem 2008, 73:8545-8552. 10.1021/jo801729p, 18855479.
    • (2008) J Org Chem , vol.73 , pp. 8545-8552
    • Fustero, S.1    Román, R.2    Sanz-Cervera, J.F.3    Simón-Fuentes, A.4    Bueno, J.5    Villanova, S.6
  • 7
    • 20444415984 scopus 로고    scopus 로고
    • Identification of antitumor activity of pyrazole oxime ethers
    • 10.1016/j.bmcl.2005.03.082, 15922597
    • Park HJ, Lee K, Park SJ, Ahn B, Lee JC, Cho H, Lee KI. Identification of antitumor activity of pyrazole oxime ethers. Bioorg Med Chem Lett 2005, 15:3307-3312. 10.1016/j.bmcl.2005.03.082, 15922597.
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 3307-3312
    • Park, H.J.1    Lee, K.2    Park, S.J.3    Ahn, B.4    Lee, J.C.5    Cho, H.6    Lee, K.I.7
  • 8
    • 33744929349 scopus 로고    scopus 로고
    • Stereoselective synthesis and antifungal activities of (E)-α-(methoxyimino)benzeneacetate derivatives containing 1,3,5- substituted pyrazole ring
    • 10.1021/jf060074f, 19127737
    • Li Y, Zhang HQ, Liu J, Yang XP, Liu ZJ. Stereoselective synthesis and antifungal activities of (E)-α-(methoxyimino)benzeneacetate derivatives containing 1,3,5- substituted pyrazole ring. J Agric Food Chem 2006, 54:3636-3640. 10.1021/jf060074f, 19127737.
    • (2006) J Agric Food Chem , vol.54 , pp. 3636-3640
    • Li, Y.1    Zhang, H.Q.2    Liu, J.3    Yang, X.P.4    Liu, Z.J.5
  • 9
    • 79953267883 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of novel pyrazole amides containing α-aminophosphonate moiety
    • Wu LT, Song BA, Bhadury PS, Yang S, Hu DY, Jin LH. Synthesis and antiviral activity of novel pyrazole amides containing α-aminophosphonate moiety. J. Heterocyclic Chem. 2011, 48:389-396.
    • (2011) J. Heterocyclic Chem. , vol.48 , pp. 389-396
    • Wu, L.T.1    Song, B.A.2    Bhadury, P.S.3    Yang, S.4    Hu, D.Y.5    Jin, L.H.6
  • 10
    • 46449089792 scopus 로고    scopus 로고
    • Spectroscopic characterization and biological activity of metal complexes with an ONO trifunctionalized hydrazone ligand
    • El-Tabl AS, El-Saied FA, Al-Hakimi AN. Spectroscopic characterization and biological activity of metal complexes with an ONO trifunctionalized hydrazone ligand. J. Coord. Chem 2008, 61:2380-2401.
    • (2008) J. Coord. Chem , vol.61 , pp. 2380-2401
    • El-Tabl, A.S.1    El-Saied, F.A.2    Al-Hakimi, A.N.3
  • 11
    • 34548385246 scopus 로고    scopus 로고
    • Biological activities of hydrazone derivatives
    • 10.3390/12081910, 17960096
    • Sevim R, Ş Güniz K. Biological activities of hydrazone derivatives. Molecules 2007, 12:1910-1939. 10.3390/12081910, 17960096.
    • (2007) Molecules , vol.12 , pp. 1910-1939
    • Sevim, R.1    Ş Güniz, K.2
  • 12
    • 78649575851 scopus 로고    scopus 로고
    • Synthesis of a novel hydrazone derivative and biophysical studies of its interactions with bovine serum albumin by spectroscopic, electrochemical, and molecular docking methods
    • 10.1021/jp105766n, 21038894
    • Tian FF, Jiang FL, Han XL, Xiang YS, Ge C, Li JH, Zhang Y, Li R, Ding XL, Liu Y. Synthesis of a novel hydrazone derivative and biophysical studies of its interactions with bovine serum albumin by spectroscopic, electrochemical, and molecular docking methods. J Phys Chem B 2010, 114:14842-14853. 10.1021/jp105766n, 21038894.
    • (2010) J Phys Chem B , vol.114 , pp. 14842-14853
    • Tian, F.F.1    Jiang, F.L.2    Han, X.L.3    Xiang, Y.S.4    Ge, C.5    Li, J.H.6    Zhang, Y.7    Li, R.8    Ding, X.L.9    Liu, Y.10
  • 13
    • 84856707437 scopus 로고    scopus 로고
    • A novel difunctional acylhydrazone with isoxazole and furan heterocycles: Syntheses, structure, spectroscopic properties, antibacterial activities and theoretical studies of (E)-N'-(furan-2-ylmethylene)-5-methylisoxazole-4-carbohydrazide
    • Jin YX, Zhong AG, Ge CHH, Pan FY, Yang JG, Wu Y, Xie M, Feng HW. A novel difunctional acylhydrazone with isoxazole and furan heterocycles: Syntheses, structure, spectroscopic properties, antibacterial activities and theoretical studies of (E)-N'-(furan-2-ylmethylene)-5-methylisoxazole-4-carbohydrazide. J. Mol. Struct. 2012, 10:190-196.
    • (2012) J. Mol. Struct. , vol.10 , pp. 190-196
    • Jin, Y.X.1    Zhong, A.G.2    Ge, C.H.H.3    Pan, F.Y.4    Yang, J.G.5    Wu, Y.6    Xie, M.7    Feng, H.W.8
  • 16
    • 77949405426 scopus 로고    scopus 로고
    • Synthesis of nalidixic acid based hydrazones as novel pesticides
    • 10.1021/jf904144e, 20131903
    • Aggarwal N, Kumar R, Srivastva C, Dureja P, Khurana JM. Synthesis of nalidixic acid based hydrazones as novel pesticides. J Agric Food Chem 2010, 58:3056-3061. 10.1021/jf904144e, 20131903.
    • (2010) J Agric Food Chem , vol.58 , pp. 3056-3061
    • Aggarwal, N.1    Kumar, R.2    Srivastva, C.3    Dureja, P.4    Khurana, J.M.5
  • 17
    • 77953146160 scopus 로고    scopus 로고
    • Design, synthesis, and insecticidal activities of phthalamides containing a hydrazone substructure
    • 10.1021/jf1000919, 20450195
    • Liu M, Wang Y, WangYang WZ, Liu F, Cui YL, Duan YS, Wang M, Liu SZ, Rui CH. Design, synthesis, and insecticidal activities of phthalamides containing a hydrazone substructure. J Agric Food Chem 2010, 58:6858-6863. 10.1021/jf1000919, 20450195.
    • (2010) J Agric Food Chem , vol.58 , pp. 6858-6863
    • Liu, M.1    Wang, Y.2    WangYang, W.Z.3    Liu, F.4    Cui, Y.L.5    Duan, Y.S.6    Wang, M.7    Liu, S.Z.8    Rui, C.H.9
  • 18
    • 27744587111 scopus 로고    scopus 로고
    • Design, synthesis and in vitro antimalarial activity of an acylhydrazone library
    • 10.1016/j.bmcl.2005.09.058, 16263280
    • Melnyk P, Leroux V, Sergheraert C, Grellier P. Design, synthesis and in vitro antimalarial activity of an acylhydrazone library. Bioorg Med Chem Lett 2006, 16:31-35. 10.1016/j.bmcl.2005.09.058, 16263280.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 31-35
    • Melnyk, P.1    Leroux, V.2    Sergheraert, C.3    Grellier, P.4
  • 19
    • 77954310776 scopus 로고    scopus 로고
    • Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety
    • 10.1016/j.ejmech.2010.04.012, 20451306
    • Ozkay Y, Tunali Y, Karaca H, Işikdaǧ I. Antimicrobial activity and a SAR study of some novel benzimidazole derivatives bearing hydrazone moiety. Eur J Med Chem 2010, 45:3293-3298. 10.1016/j.ejmech.2010.04.012, 20451306.
    • (2010) Eur J Med Chem , vol.45 , pp. 3293-3298
    • Ozkay, Y.1    Tunali, Y.2    Karaca, H.3    Işikdaǧ, I.4
  • 20
    • 62549084279 scopus 로고    scopus 로고
    • Novel pyridazine derivatives: synthesis and antimicrobial activity evaluation
    • 10.1016/j.ejmech.2008.09.047, 19013692
    • Kandile NG, Mohamed MI, Zaky H, Mohamed HM. Novel pyridazine derivatives: synthesis and antimicrobial activity evaluation. Eur J Med Chem 2009, 44:1989-1996. 10.1016/j.ejmech.2008.09.047, 19013692.
    • (2009) Eur J Med Chem , vol.44 , pp. 1989-1996
    • Kandile, N.G.1    Mohamed, M.I.2    Zaky, H.3    Mohamed, H.M.4
  • 21
    • 84859420549 scopus 로고    scopus 로고
    • Design, synthesis, insecticidal activity and CoMFA study of novel pyrazole amides containing hydrazone substructure
    • 10.1002/ps.2329, 22190278
    • Wu J, Song BA, Hu DY, Yue M, Yang S. Design, synthesis, insecticidal activity and CoMFA study of novel pyrazole amides containing hydrazone substructure. Pest Manag Sci 2012, 68:801-810. 10.1002/ps.2329, 22190278.
    • (2012) Pest Manag Sci , vol.68 , pp. 801-810
    • Wu, J.1    Song, B.A.2    Hu, D.Y.3    Yue, M.4    Yang, S.5
  • 22
    • 84859378892 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity against ralstonia solanacearum for novel hydrazone derivatives containing a pyridine moiety
    • 10.1186/1752-153X-6-28, 3359257, 22483270
    • Wu J, Kang SH, Song BA, Hu DY, He M, Jin LH, Song Y. Synthesis and antibacterial activity against ralstonia solanacearum for novel hydrazone derivatives containing a pyridine moiety. Chemistry Central Journal. 2012, 6:28. 10.1186/1752-153X-6-28, 3359257, 22483270.
    • (2012) Chemistry Central Journal. , vol.6 , pp. 28
    • Wu, J.1    Kang, S.H.2    Song, B.A.3    Hu, D.Y.4    He, M.5    Jin, L.H.6    Song, Y.7


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