PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Powiadomienia systemowe
  • Sesja wygasła!
Tytuł artykułu

Spectral and Microbial Studies of some Newly Synthesized Schiff Base Derivatives of 2-(1H-benzo[d]oxazole-2-ylthio)-N-(4-acetylphenyl)acetamide

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The author has synthesized novel biological active compounds by condensation of N-(4-Acetyl-phenyl)-2-(benzooxazol-2-ylsulfanyl)-acetamide with defferent substituted of acid hydrazide in the presence of catalytic amount of acetic acid. A series of benzoxazole having azomethine group were confirmed by various spectroscopic techniques. The new compounds were examined for antibacterial effects again different strain of bacteria and antifungal were high to lowest Minimum Inhibition Concentration (MIC) values.
Słowa kluczowe
Rocznik
Tom
Strony
57--65
Opis fizyczny
Bibliogr. 16 poz., tab., wz.
Twórcy
autor
  • Department of Chemistry, Sheth M. N. Science College, NGES campus, Patan - 384265, India
autor
  • Department of Chemistry, Sheth M. N. Science College, NGES campus, Patan - 384265, India
autor
  • Department of Chemistry, Sheth M. N. Science College, NGES campus, Patan - 384265, India
Bibliografia
  • [1] T. Panneer Selvam, P. P. Radhika, S. Janagaraj, A. Siva Kumar, Research In biotechnology 2 (2011) 50-57.
  • [2] Pedrazzini S, De Angelis M, Muciaccia WZ, Sacchi C, Forgione A, Arzneimittel-Forschung 38 (8): 1170–5. PMID 3196413
  • [3] Samia M. Rida, Fawzia A. Ashour, Soad A.M. El-Hawash, Mona M. ElSemary, Mona H. Badr, Manal A. Shalaby, Eur J Med Chem 40 (2005) 949-959.
  • [4] Jarmila Vinsova, Vaclav Horak, Vladimir Buchta and Jarmila Kaustova, Molecules 10 (2005) 783-793.
  • [5] Meric Koksal, Nesrin Gokhan, Esra Kupeli, Erdem Yesilada, and Hakki Erdogan, Arch Pharm Res. 30 (2007) 419-424.
  • [6] Mimnaugh, E.G.; Xu, W.; Vos, M. Mol. Cancer Ther. 3 (2004) 551–566.
  • [7] Yadav, R; Sirvastava, SD and Sirvastava, SK (2005), Indian J. Chem. 44 (2005) 1262-1266.
  • [8] Ramón, G; Domenech, B; Ana, C; Gregori, C and Calabuig, C, Internet Electron. J. Mol. Des., BioChem Press,1 (2002) 339-350.
  • [9] R. V. Satyendra, K. A. Vishnumurthy, H. M. Vagdevi, K. P. Rajesh, H. Manjunatha,and A. Shruthi, European Journal of Medicinal Chemistry 46 (2011) 3078–3084.
  • [10] Paramashivappa R, Phanikumar P, Subbarao P, Srinivasarao A, Bioorg Med Chem Lett. 13, 2003, 657-660.
  • [11] Grocer, H., Kus, C., Boykin, D.W., Yildiz, S., Altanlar, N., Bioorg. Med. Chem.10 (2002) 2589-2596.
  • [12] Nicholson R. M, Murphy J. R, Dearden J. R, Journal of Pharmacy and Pharmacology 34 (1982) 106-111.
  • [13] Fang, B., Zhou, C.H., Rao, X.C., Eur. J. Med. Chem. 45 (2010) 4388-4398.
  • [14] E. F. Magomedova, V. V. Pinyaskin, A. Sh. Aminova, Pharma. Chem. J. 41 (2007) 474-475.
  • [15] Kalpesh Parikh, Deepkumar Joshi, Med Chem Res. 22 (2013) 3688-3697.
  • [16] P.C. Hannan, Vet. Res. 31 (2000) 373-395.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f2d0a7f4-6ffd-4358-87f8-2d4fe7fff97b
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.