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Synthesis, Characterization and Biological evaluation of some newer 5-[6-chloro/fluoro/nitro-2-(p-chloro/ fluoro/ methyl phenyl)-quinolin-4-yl]-1,3,4-oxadiazole-2-thiols

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Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Recent study shows that quinolines represent one of the most active classes of compounds possesses wide spectrum biodynamic activities and use as potent therapeutic agents. In present research work, 5-[6-chloro/fluoro/nitro-2-(p-chloro/fluoro/methyl phenyl)-quinolin-4-yl]-1,3,4-oxadiazole-2-thiols have been synthesized by condensation of substituted quinoline-4-carbohydrazides and mixture of carbon disulphide and potassium hydroxide. All of these compounds were screened for their in vitroanti microbial 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
26--32
Opis fizyczny
Bibliogr. 21 poz., tab., wz.
Twórcy
autor
  • 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
  • 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] F. Salem, J. Drug Res 12 (1980) 101.
  • [6] P. Stocks, K. Raynes, P. Bray, B. Kevin Park, P. O’Neill, S. Ward, J. Med. Chem. 45 (2002) 4975.
  • [7] 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.
  • [8] 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.
  • [9] Schnute E. Mark, PTC int Appl. Wo 01 98 (2001) 275.
  • [10] B. Chaudhari, M. Chapdeline, G. Hostetler, L. Kemp, J. McCauley, PTC int Appl. Wo 02 36 (2000) 586.
  • [11] M. Chapdeline, J. McCauley, PTC int Appl. Wo 02 36 (2000) 576.
  • [12] G. Lesher, E. Froelich, M. Gruet, J. Baily, 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] N. Gularman, S. Rollas, H. Erdeniz, M. Kiraz, Journal of Pharmaceutical Sciences 26 (2001) 1.
  • [18] A. Foroumadi, M. Danstalab, M. Mahamoudian, M. Falahati, N. Nateghian, N. Shahsavarani, A. Shafiee, Pharm. Pharmacol. Commun 4 (1998) 95.
  • [19] N. Habib, R. Soliman, F. Ashour, M. El-Taiebi, Die Pharmazie 52 (1997) 746.
  • [20] A. Trivedi, V. Bhuva, B. Dholariya, D. Dodiya, V. Kataria, V. Shah, Bioorganic & Medicinal Chemistry Letters 20 (2010) 6100.
  • [21] G. Alamelumangai, N. Santhi, International Letters of Chemistry, Physics and Astronomy 5 (2014) 124-133.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-c86b8a52-6faf-44fe-9ca0-e073c2cb64a5
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