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Synthesis and in vitro antimicrobial evaluation of amine substituted s-triazine based thiazolidinone/chalcone hybrids

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In an attempt to control multidrug resistant dilemma, a library of s-triazine based on two novel series of thiazolidinone (4a-e) and chalcone (7a-e) derivatives were designed and synthesized with simple and efficient etiquette. The newly synthesized compounds were studied for efficacy against several bacteria (Staphylococcus Aureus, Bacillus Cereus, Pseudomonas Aeruginosa, Klebsiella Pneumoniae,) and fungi (Candida Albicans, Aspergillus Clavatus) using the broth dilution technique. Compound 7d was the best bioactive desired antibacterial analogue with less MIC value against different tested strains. Results of bioassay study revealed the future hope of the potent drug-candidate based on s-triazine scaffold. All the final synthesized compounds were characterized by IR, 1 H NMR, 13 C NMR, mass and elemental analysis.
Słowa kluczowe
Rocznik
Strony
207--219
Opis fizyczny
Bibliogr. 21 poz., rys., wz.
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] D.R. Shah, R.P. Modh, K.H. Chikhalia, Future med. chem. 6 (2014) 463-477.
  • [2] H.R. Bhat, P.K. Pandey, S.K. Ghosh, U.P. Singh, Med. Chem. Res. 22 (2013) 5056-5065.
  • [3] A.D. Desai, D.H. Mahajan, K.H. Chikhalia, Ind. J. Chem. Sec. B 46 (2007) 1169.
  • [4] P. Gahtori, S.K. Ghosh, P. Parida, A. Prakash, K. Gogoi, H.R. Bhat, U.P. Singh, Exp. Parasitol. 130 (2012) 292-299.
  • [5] A. Baliani, G.J. Bueno, M.L. Stewart, V. Yardley, R. Brun, M.P. Barrett, I.H. Gilbert, J. Med. Chem. 48 (2005) 5570-5579.
  • [6] U.P. Singh, H.R. Bhat, P. Gahtori, J. Mycol. Med. 22 (2012) 134-141.
  • [7] R. Menicagli, S. Samaritani, G. Signore, F. Vaglini, L. Dalla Via, J. Med. Chem. 47 (2004) 4649-4652.
  • [8] A.B. Patel, R.V. Patel, P. Kumari, D.P. Rajani, K.H. Chikhalia, Med. Chem. Res. 22 (2012) 367-381.
  • [9] X. Chen, P. Zhan, X. Liu, Z. Cheng, C. Meng, S. Shao, C. Pannecouque, E. De Clercq, Bioorg. Med. Chem. 20 (2012) 3856-3864.
  • [10] Y.-Z. Xiong, F.-E. Chen, J. Balzarini, E. De Clercq, C. Pannecouque, Eur. J. Med. Chem. 43 (2008) 1230-1236.
  • [11] X. Chen, P. Zhan, C. Pannecouque, J. Balzarini, E. De Clercq, X. Liu, Eur. J. Med. Chem. 51 (2012) 60-66.
  • [12] R.V. Patel, P. Kumari, D.P. Rajani, K.H. Chikhalia, J. FLUORINE CHEM. 132 (2011) 617-627.
  • [13] R.V. Patel, P. Kumari, D.P. Rajani, K.H. Chikhalia, Eur. J. Med. Chem. 46 (2011) 4354-4365.
  • [14] S. Kumar, H.R. Bhat, M.K. Kumawat, U.P. Singh, New J. Chem. 37 (2013) 581-584.
  • [15] A. Solankee, K. Kapadia, A. Ćirić, M. Soković, I. Doytchinova, A. Geronikaki, Eur. J. Med. Chem. 45 (2010) 510-518.
  • [16] T.D. Gootz, Crit. Rev. Immunol. 30 (2010) 79-93.
  • [17] K.M. Overbye, J.F. Barrett, Drug Discov. Today 10 (2005) 45-52.
  • [18] D. Niccolai, L. Tarsi, R. J. Thomas, Chem. Commun. (1997) 2333-2342.
  • [19] C. Nathan, Nature 431 (2004) 899-902.
  • [20] M.C. Raviglione, Tuberculosis 83 (2003) 4.
  • [21] P. Hawkey, D.A. Lewis, Medical Bacteriology: A Practical Approach, Oxford University Press, Oxford, 2004.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b126c1cc-d206-488a-8b01-a1c720593645
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