Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2016 | 71 | 2 |

Article title

Synthesis, spectral LFER and antimicrobial activities of some (E)-N׳-(1-(substituted phenyl)ethylidene)benzohydrazides

Content

Title variants

Languages of publication

EN

Abstracts

EN
About eleven substituted (E)-N׳-(1-(substituted phenyl) ethylidene) benzo- hydrazides have been synthesized. They are characterized by their analytical, ultraviolet, infrared and NMR spectral data. The antibacterial and fungal activities of these chalcones have been evaluated.

Keywords

EN

Year

Volume

71

Issue

2

Physical description

Dates

published
2016
online
2017-04-03

References

  • W. O. Foye, Principles of Medicinal Chemistry, Varghese Publishing House, Bombay, III, Ed., 629, (1989).
  • I. S. Berdinskii, Chem. Heterocyclic Comp., 15(2), 238, (1979).
  • V. Polshettiwar, R. S. Varma, Tetrahedron Lett., 48(32), 5649, (2007).
  • S. Rollas, S. G. Kucukguzel, Molecules., 12, 1910, (2007).
  • L. Savini, L. Chiasserini, V. Travagli, C. Pellerano, E. Novellino, S. Cosentino, M. B.Pisano, Eur. J. Med. Chem., 39, 113, (2004).
  • V.L. Gein, L.F. Gein, M.V. Chirkova, V.A. Mikhalev, E.V. Voronina, Pharma. Chem. J., 39(8), 413, (2005).
  • H. Bayrak, A. Demirbas, N. Demirbas, S. A. Karaoglu, Eur. J. Med. Chem., 44, 4362, (2009).
  • B. Narasimhan, P. Kumar, D. Sharma, ActaPharmaceuticaSciencia, 52, 169, (2010).
  • P. Melnyk, V. Leroux, C. Sergheraert, P. Grellier, Bioorg. Med. Chem. Lett., 16, 31, (2006).
  • A. Nayyar, V. Monga, A. Malde, E. Coutinho, R. Jain, Bioorg. Med. Chem., 15, 626, (2007).
  • A. Imramovsky, S. Polanac, J. Vinsova, M. Kocevar, J. Jampitek, Z. Reckova, J. A. Kaustova, Bioorg. Med. Chem., 15, 2551, (2007).
  • Y. Janin, Bioorg. Med. Chem., 15, 2479, (2007).
  • J.P. Raval, N.H. Patel, H.V. Patel, P.S. Patel, Med. Chem. Res, DOI: 10.1007/s00044- 010-9324-3, (2010).
  • A. Bijev, Lett. Drug. Des. Discov., 3, 506, (2006).
  • U. Salgin-Goksen, N. Gokhan-Kelekci, O. Goktas, Y. Koysal, E. Kılıc, S. Isik.
  • G. Aktay, M. L. Ozalp, Bioorg. Med. Chem., 15, 5738, (2007).
  • R. Kalsi, M. Shrimali, T. N. Bhalla, J. P. Barthwal, Ind. J. Pharm. Sci., 52, 129, (1990).
  • Y. Xia, C.D. Fan, B.X. Zhao, J. Zhao, D.S. Shin, J.Y. Miao, Eur. J. Med. Chem., 43, 2347, (2008).
  • L. Troeberg, X. Chen, T.M. Flaherty, R.E. Morty, M. Cheng, H. Hua, C. Springer, J.H. McKerrow, G.L. Kenyon, J.D. Lonsdale-Eccles, T.H.T. Coetzer, F.E. Cohen, Mol. Med., 6, 660, (2000).
  • M. V. Lembege, S. Moreau, S. Larrouture, D. Montaudon, J. Robert, A. Nuhrich, Eur. J. Med. Chem., 43, 1336, (2008).
  • W. Porcal, P. Hernandeez, L. Boiani, M. Boiani, A. Ferreira, A. Chidichimo, J. J. Cazzulo, C.O. Azar, M. Gonzalez, H. Cerecetto, Bioorg. Med. Chem., 16, 6995, (2008).
  • J. Easmon, G. Purstinger, K.S. Thies, G. Heinisch, J. Hoffman, J. Med. Chem., 49, 6343, (2006).
  • P. C. Lima, L. M. Lima, K. C. M. da Silva, P. H. O. Leda, A. L. P. de Miranda, C. A. M. Fraga, E. J. Barreiro, Eur. J. Med. Chem., 35, 187, (2000).
  • S. G. Kucukguzel, A. Mazi, F. Sahin, S. Ozturk, J. Stables, Eur. J. Med. Chem., 38, 1005, (2003).
  • S. P. Sakthinathan, R. Suresh, V. Mala, K. Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, S. John Joseph, G. Vanangamudi, G. Thirunarayanan., Int. J. Sci. Res. Know., 1(11), 472, (2013).
  • S. P. Sakthinathan, R. Suresh, V. Mala, K. Sathiyamoorthi, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, S. Vijayakumar, R. Sundararajan, G. Vanangamudi, G. Thirunarayanan., Inter. Lett. Chem. Phy. Astro., 6, 77, (2013).
  • R. Suresh, D. Kamalakkannan, K. Ranganathan, R. Arulkumaran, R. Sundararajan, S. P. Sakthinathan, S. Vijayakumar, K. Sathiyamoorthi, V. Mala, G. Vanangamudi, K. Thirumurthy, P. Mayavel, G. Thirunarayanan, Spectrochim. Acta, 101A, 239, (2013).
  • R. Arulkumaran, S. Vijayakumar, S. P. Sakthinathan, D. Kamalakkannan, K. Ranganathan, R. Suresh, R. Sundararajan, G. Vanangamudi, G. Thirunarayanan, J. Chil. Chem. Soc., 2, 58, (2013).G. Thirunarayanan, M. Gopalakrishnan, G. Vanangamudi, Spectrochemica Acta., 67A, 106, (2007).
  • S. P. Sakthinathan, G. Vanangamudi and G. Thirunarayanan, Spectrochim. Acta, 95A, 693, (2012).
  • S. Sasikala, K. Thirumurthy, P. Mayavel and G. Thirunarayanan, Org. Med. Chem. Lett.: 2012. doi:10.1186/2191-2858-2-20.
  • G. Thirunarayanan, P. Mayavel, K. Thirumurthy, S. Dineshkumar, R. Sasikala, P. Nisha and A. Nithyaranjani, European Chem. Bull., 2(9), 598, (2013).
  • G. Thirunarayanan and K. G. Sekar, J. Taibah Univ. Sci. 8, 124, (2014).
  • M. Rajarajan, R. Vijayakumar, R. Senbagam, S. Balaji, V. Manikandan, G. Vanangamudi and G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 59, 147, (2015).
  • R. Vijayakumar, M. Rajarajan, R. Senbagam, S. Balaji, V. Manikandan, G. Vanangamudi and G. Thirunarayanan, Int. Lett. Chem. Phys. Astro. 59, 199 (2015).
  • A. W. Bauer, W. M. M. Kirby, J. C. Sherris, M. Truck, Am. J. Clin. Patho., 45, 493, (1966).
  • C. G. Swain, E. C. Lupton, J. Am. Chem. Soc., 90, 4328, (1968).

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.ojs-doi-10_17951_aa_2016_71_2_29
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.