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Synthesis, characterization, antibacterial evaluation and molecular docking studies of 2-azetidinone derivatives as novel DNA gyrase inhibitors

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Newly designed 2-azetidinone derivatives (4a-e) were synthesized in good yields and characterised by advanced spectroscopic studies. The title compounds were evaluated for qualitative (zone of inhibition) by agar diffusion method against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa and Streptococcus pyogenes. Some of the analogues were found to have comparable or even more potency than the standard drugs. Docking study was performed to check interaction of synthesized compounds with the target DNA gyrase.
Rocznik
Tom
Strony
94--108
Opis fizyczny
Bibliogr. 13 poz., fot., tab., wykr., wz.
Twórcy
  • Department of Chemistry, Government Arts College, Chidambaram - 608102, India
autor
  • Department of Chemistry, Government Arts College, Chidambaram - 608102, India
Bibliografia
  • [1] Sumit Bansal et al., Design, Synthesis, Docking Study & Antibacterial Evaluation of 1,3- Diarylpyrazolyl Substituted Indolin-2-ones, Indo Global Journal of Pharmaceutical Sciences, 2014; 4(1): 1-7
  • [2] Kilarimath Basavaraj et al., Synthesis, Docking and Antitubercular Activity of some newer Azetidinones, Unique journal of pharmaceutical and biological sciences, 2014, 02 (01); 43-50
  • [3] Sharma et al., N/C-4 substituted azetidin-2-ones: Synthesis and preliminary evaluation as new class of antimicrobial agents, Bioorg. Med. Chem. Lett. 2007, 17, 341–345.
  • [4] Gurupadayya B M et al., Synthesis and Pharmacological Evaluation of Azetidin-2-ones and Thiazolidin-4-ones Encompassing Benzothiazole, Indian J. Pharm. Sci. 2008, 70 (5), 572–577.
  • [5] Rajasekaran, A., Murugesan, S, Synthesis and characterization of some novel azetidinone derivatives as anti-bacterial and anti-convulsant agents, J. Pharm. Bioresour. 20052 (2), 162–168.
  • [6] Rosenblum, S.B., Huynh, T., Afonso, A., Davis H.R., Synthesis of 3-arylpropenyl, 3- arylpropynyl and 3-arylpropyl 2- azetidinones as cholesterol absorption inhibitors: application of the palladium-catalyzed arylation of alkenes and alkynes. Tetrahedron ., 2000. 56, 5735–5742.
  • [7] Jyotsna Meshram et al., Microwave Mediated Cyclocondensation of 2-aminothiazole into β- lactam Derivatives: Virtual Screening and In Vitro Antimicrobial Activity with Various Microorganisms, Int.J. ChemTech Res.2010,2(2),231-237
  • [8] Smita pawar et al., Synthesis of novel antimicrobial derivatives of 3-substituted pyrrolidine2, 5-diones using pharmacophore hybrid approach: part-I, Int J Pharm Pharm Sci,2014, 6(2), 486-490
  • [9] Amit Poshiya et al, Synthesis studies of bacterial dna-gyrase inhibitors, IJPT, 2011 3(3) 3048-3059
  • [10] E.W. Koneman, S.D. Allen, W.M. Janda, P.C. Schreckenberger, Colour Atlas and Text Book of Diagnostic Microbiology, 5th ed., Jt. Editor W.C. Winn, Lippincott, Philadelphia, P.A., 1997,185.
  • [11] V. Cleidson, M. Simone, F.A.S. Elza Artur S. Jr., Braz. J.microbiol., 2007, 38(2), 369-380.
  • [12] Daisy P, Vijayalakshmi P, Selvaraj C, Singh SK, Saipriya K. Targeting Multidrug Resistant Mycobacterium Tuberculosis Htra2 With Identical Chemical Entities Of Fluoroquinolones, Indian Journal Of Pharmaceutical Sciences 2012; 74(3): 189-280
  • [13] Pandurangan Perumal et al., Docking Studies on Some Novel Piperidine Analogues Against DNA Gyrase Enzyme., Inventi Rapid: Molecular Modeling 2014, 1, 256-260
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-adeadc57-21df-4cef-a39f-0235730f34c8
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