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Tytuł artykułu

Synthesis, Spectral Analysis and Evolution of Antimicrobial Activity of Schiff Base of Cyanoacetohydrazide

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In search of some antimicrobial agents, synthesis of some Schiff base of cyanoacetohydrazide derivatives has been reported. The structures of all the synthesized compounds were established on the bases of various spectroscopic methods. All Schiff base were screened for antimicrobial activity. cyanoacetohydrazide were found to possess better antimicrobial potential.
Rocznik
Tom
Strony
100--110
Opis fizyczny
Bibliogr. 15 poz., rys., wz.
Twórcy
autor
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005
autor
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005
autor
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005
autor
  • Chemical Research Laboratory, Department of Chemistry Saurashtra University, Rajkot - 360005
Bibliografia
  • [1] S. Rallas, N. Gulerman, H. Erdeniz, Farmaco 57 (2002) 171-174.
  • [2] A. Gursoy, N. Terzioglu, G. Otuk, Eur. J. Med. Chem. 32 (1997) 753-757.
  • [3] C. Walsh, Nature 406 (2000) 775-778.
  • [4] S. Rollas, N. Kalyoncuoğlu, D. Sur-Altiner and Y. Ye- ğenoğlu, Pharmazie, Vol. 48, No. 4, (1993), 308-309.
  • [5] S. Papakonstantinou-Garoufalias, N. Pouli, P.-Marakos and A. Chytyro-Glouladas, Farmaco, Vol. 57, No. 12, (2002), pp. 973-977.
  • [6] M. Kidwai, R. Kumar, A. Srivastava and H. P. Gupta, Bioorganic Chemistry, Vol. 26, No. 5, (1998), pp. 289-294.
  • [7] V. V. Kachhadia, M. R. Patel and H. S. Joshi, Journal of the Serbian Chemical Society, Vol. 70, No. 2, (2005), pp. 153-161.
  • [8] P. K. KadabaCurrent Medicinal Chemistry, Vol. 10, No. 20, (2003), pp. 2081-2108.
  • [9] İ. küçükgüzel, Ş. G. Küçükgüzel, S. Rollas, G. Ö.-Saniş, O. Özdemir, I. Bayrak, T. Altuğand J. P. Stables, Farmaco, Vol. 59, No. 11, (2004), pp. 893-901.
  • [10] M. D. Mullican, M. W. Wilson, D. T. Connor, C. R. Kostlan, D. J. Schrier and R. D. Dyer, Journal of Medicinal Chemistry, Vol. 36, No. 8, (1993), pp. 1090-1099.
  • [11] E. Palaska, G. Şahin, P. Kelicen, N. T. Durlu and G. Altinok, Farmaco, Vol. 57, No. 2, (2002), pp. 101-107.
  • [12] A.Varvaresou, T. Siatra-Papastaikoudi, A. Tsotinis, A. TsantiliKakoulidou and A. Vamvakides, Farmaco, Vol. 53, No. 5, (1989), pp. 320-326.
  • [13] B. S. Holla, B. Veerendra, M. K. Shivanada and B. Poo- jary, european Journal of Medicinal Chemistry, Vol. 38, No. 7-8, (2003), pp. 759-767.
  • [14] J. H. Lange, H. H. Stuivenberg, H. K. Coolen, T. J. Adolfs, A. C. McCreary, H.G. Keizer, H. C. Wals, W.Veerman, A. J. Borst, W. de Looff, P. C. Verveer and C. G. Kruse, Journal of Medicinal Chemistry, Vol. 48, No. 6, (2005), pp. 1823-1838.
  • [15] N. Szuber, J.L. Buss, S.S. Lin, H. Felfly, M. Trudel, P. Ponka, Exp. Hematol. 36(2008) 773–785.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-7a501b8e-5a19-4e6c-b200-715bf9716670
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