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Synthesis, characterization of biologically potent novel chalcones bearing urea, thiourea and acetamide linkages

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Three series of some novel chalcone based urea, thiourea and acetamide derivatives were designed, synthesized and screened for their antimicrobial and antifungal activities. All the synthesized compounds are first reported. The structures of the compounds were elucidated with the aid of elemental analysis and spectral methods including IR, 1H-NMR spectral data. The prepared compounds were evaluated for antibacterial activity against two Gram-positive bacteria (Staphylococcus aureus, Staphylococcus pyogenus), two Gram-negative bacteria (Pseudomonas aeruginosa, Escherichia coli). The title compounds were also investigated for their antifungal activity using the broth micro dilution method. The bioassay results showed that compounds a few compounds showed good to superior in vitro antibacterial and antifungal activity.
Rocznik
Strony
281--294
Opis fizyczny
Bibliogr. 25 poz., rys., tab.
Twórcy
autor
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabed-380009, Gujarat, India
autor
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabed-380009, Gujarat, India
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabed-380009, Gujarat, India
Bibliografia
  • [1] J.H. Cheng, C.F. Hung, S.C. Yang, J.P. Wang, S.J. Won, C.N. Lin, Bioorg. Med. Chem. 16 (2008) 7270-7276.
  • [2] K. H. Chikhalia, M. J. Patel, D. B. Vashi, ARKIVOC 13 (2008) 189-197.
  • [3] C. Zhan, J. Yang, Pharmacol. Res. 53 (2006) 303-309.
  • [4] M. Liu, P. Wilairat, M.L. Go, J. Med. Chem. 44 (2001) 4443-4452.
  • [5] M.L. Go, X. Wu, X.L. Liu, Curr. Med. Chem. 12 (2001) 481-499.
  • [6] V.S. Koneni, K. Abdhesh, K. Manoj, S. Jayanta, S. Sudhir, Bioorg. Med. Chem. Lett. 20 (2010) 7205-7211.
  • [7] P. A. Yonova, G. M. Stoilkova, J. Plant Growth Regul. 23 (2004) 280-291.
  • [8] Y. J. Kim, J. H. Ryu, Y. J.Cheon, H. J. Lim, R. Jeon, Bioorg. Med. Chem. Lett. 17 (2007) 3317-3321.
  • [9] O. Adeoye, A. A. Ayandele, O. A. Odunola, J. Agric. Biol. Sci. 2 (2007) 4-5.
  • [10] T. K. Venkatachalam, C. Mão, F. M. Uckun, Bioorg. Med. Chem. 12 (2004) 4275- 4284.
  • [11] J. D. Bloom, R. G. Dushin, K. J. Curran, F. Donahue, E. B. Norton, E. Terefenko, T. R. Jonas, A. A. Ross, B. Feld, S. A. Lang, M. J. Di-Grandi, Bioorg. Med. Chem. 14 (2004) 3401-3406.
  • [12] C. Furman, J. Lebeau, J. C. Fruchart, J. L. Bernier, P. Duriez, N. Cotelle, E. Teissier, E. J. Biochem. Mol. Toxicol. 15 (2001) 270-278.
  • [13] J. Rojas, M. Paya, J. N. Domínguez, L. Ferrandiz, Bioorg. Med. Chem. Lett. 12 (2002) 1951-1954.
  • [14] J. Rojas, M. Paya, L. Devesa, J. N. Domínguez, L. Ferrandiz, Naunyn- Schmiedeberg’s Arch. Pharmacol. 368 (2003) 225-233.
  • [15] A. Araico, M. C. Terencio, M. J. Alcaraz, J. N. Dominguez, C. León, M. L. Ferrándiz, Life Sci. 80 (2007) 2108-2117.
  • [16] J. N. Dominguéz, C. León, J. Rodrigues, N. Gamboa de Dominguez, J. Gut, P. G. Rosenthal, J. Med. Chem. 48 (2005) 3654-3658.
  • [17] J.H. Clark, H. L. Holland, J.M. Miller, Tetrahedron Lett. 38 (1978) 3361-3364.
  • [18] H. S. Bodiwala, S. Sabde, P. Gupta, R. Mukherjee, R. Kumar, P. Garg, K. K. Bhutani, D. Mitram I. P. Singh, Bioorg. Med. Chem. 19 (2011) 1256.
  • [19] G. Thirunarayanan, K. G. Sekar, International Letters of Chemistry, Physics and Astronomy 10(1) (2013) 18-34.
  • [20] S. Vijayakumar, R. Arulkumaran, R. Sundararajan, S. P. Sakthinathan, R. Suresh, D. Kamalakkannan, K. Ranganathan, K. Sathiyamoorthy, V. Mala, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 9(1) (2013) 68-86.
  • [21] R. Sundararajan, R. Arulkumaran, S. Vijayakumar, D. Kamalakkannan, R. Suresh, S. John Joseph, K. Ranganathan, S. P. Sakthinathan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 1 (2014) 67-73.
  • [22] K. G. Sekar, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 8(3) (2013) 249-258.
  • [23] G. Thirunarayanan, K. Ravi, International Letters of Chemistry, Physics and Astronomy 14 (2013) 44-57.
  • [24] S. P. Sakthinathan, R. Suresh, V. Mala, K.Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, S. Vijayakumar, R. Sundararajan, G. Vanangamudi, G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 6 (2013) 77-90.
  • [25] G. Thirunarayanan, R. Sundararajan, R. Arulkumaran, International Letters of Chemistry, Physics and Astronomy 4 (2014) 82-97.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-da513658-c163-4c77-bb62-733ae5a24323
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