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Synthesis, Characterization and Biological evaluation of 6-substituted-2-(substituted-phenyl)-quinoline derivatives bearing 4-amino-1,2,4-triazole-3-thiol ring at C-4 position

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Quinoline derivatives represent one of the most active classes of compounds possesses wide spectrum biodynamic activities and use as potent therapeutic agents. In this research work, a synthesis, characterization and biological evaluation of 6-substituted-2-(substituted-phenyl)-quinoline derivatives bearing 4-amino-1,2,4-triazole-3-thiol ring at C-4 position is described. The synthesis of quinoline derivatives is carried out by the reaction of substituted quinoline-4-carbohydrazides with a mixture of carbon disulphide and potassium hydroxide which further react with hydrazine hydrate to give final compounds. All of these compounds were screened for their in vitro antimicrobial assay against gram (+ve), gram (-ve) bacteria and fungi activity compared with standard drugs viz., Ampicilin, Chloramphenicol, Ciprofloxacin, Norfloxacin, Griseofulvin and Nystatin at different concentrations.
Rocznik
Tom
Strony
30--37
Opis fizyczny
Bibliogr. 24 poz., tab.
Twórcy
  • Department of Chemistry, Saurashtra University, University Road, Rajkot 360 005, Gujarat, India
  • Department of Chemistry, Saurashtra University, University Road, Rajkot 360 005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, University Road, Rajkot 360 005, Gujarat, India
Bibliografia
  • [1] P. Donald, P. Van Helden, N Engl J Med 360 (2009) 2393-2395.
  • [2] R. Tripathi, N. Tewari, N. Dwivedi, V. Tiwari, Med Res Rev 25 (2005) 93-131.
  • [3] Y. Zhang, K. Post-Martens S. Denkin, Drug Discov Today 11 (2006) 21-27.
  • [4] http://www.who.int, 2007.
  • [5] J. Polanski, F. Zouhiri, L. Jeanson, D. Desmaële, J. d'Angelo, J. Mouscadet, R. Gieleciak, J. Gasteiger, M. Le Bret, Journal of medicinal chemistry 45(21) (2002) 4647-4654.
  • [6] Schnute, E. Mark, PTC int Appl. Wo 01 98 (2001) 275.
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  • [8] B. Chaudhari, M. Chapdeline, G. Hostetler, L. Kemp, J. McCauley, PTC int Appl. Wo 02 36 (2000) 586.
  • [9] M. Chapdeline, J. McCauley, PTC int Appl. Wo 02 36 (2000) 576.
  • [10] P. Stocks, K. Raynes, P. Bray, B. Kevin Park, P. O’Neill, S. Ward, J. Med. Chem. 45 (2002) 4975.
  • [11] R. Ridley, W. Hofheinz, H. Matile, C. Jaquet, A. Dorn, R. Masciadri, S. Jolidon, W. Richter, A. Guenzi, M. Girometta, Antimicrobial agents and chemotherapy 40(8) (1996) 1846-1854.
  • [12] G. Lesher, E. Froelich, M. Gruet, J. Baily, and R. Brudage, J. med. pharm. Chem 5 (1962) 1068.
  • [13] Holzgrabe, U, Steinert, M, Die Pharmazie 56 (11) (2001) 850.
  • [14] K. Fang, Y. Chen, J. Sheu, T. Wang, C. Tzeng, Journal of medicinal chemistry 43 (20) (2000) 3809-3812.
  • [15] Y. Chen, K. Fang, J. Sheu, S. Hsu, C. Tzeng, Journal of medicinal chemistry 44 (2001) 2371.
  • [16] Belal, F, Al-Majed, A, Al-Obaid, A, Talanta 50(4) (1999) 765-786.
  • [17] H. Bayrak, A.Demirbas, S. A. Karaoglu, N. Demirbas, European journal of medicinal chemistry 44(3) (2009) 1057-1066.
  • [18] A. Hasan, N. F. Thomas, S. Gapil, Molecules, 16(2) (2011) 1297-1309.
  • [19] Z. Khiati, A. A. Othman, B. Guessas, South African Journal of Chemistry 60 (2007).
  • [20] Rahul R. Tripathi, Ratnamala P. Sonawane, International Letters of Chemistry, Physics and Astronomy 10(2) (2013) 119-125.
  • [21] Mallikarjun S. Yadawe, Shrishila N. Unki, Sangamesh A. Patil, International Letters of Chemistry, Physics and Astronomy 12 (2013) 94-104.
  • [22] G. Thirunarayanan, International Letters of Chemistry, Physics and Astronomy 5 (2014) 89-98.
  • [23] V. J. Faldu, P. K. Talpara, N. H. Bhuva, P. R. Vachharajani, V. H. Shah, International Letters of Chemistry, Physics and Astronomy 6 (2014) 26-32.
  • [24] Piyush B. Vekariya, Jalpa R. Pandya, Vaishali Goswami, Hitendra S. Joshi, International Letters of Chemistry, Physics and Astronomy 7 (2014) 45-52.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-7a3174b9-a3fa-4762-a009-499de8e08665
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