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Synthesis And Antibacterial Activities Of Benzothiazole Derivatives Of Sulphonamides


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[1], F. Prestinaci, P. Pezzotti, A. Pantosti, “Antimicrobial resistance: a global multifaceted phenomenon. Pathogens and Global Health, 2015, 109(7), 309-318”. https://doi.org/10.1179/2047773215Y.000000003010.1179/2047773215Y.0000000030476862326343252Search in Google Scholar

[2] World Health Organisation. Antimicrobial resistance: Fact sheet.. 2018. www.who.int/en/news-room/fact-sheets/detail/antimicrobial-resistanceSearch in Google Scholar

[3] D. S. Doğruer, S. Urlu, T. Önkol, B. Özçelik, M. F. Şahin, “Synthesis of some pyridazine derivatives carrying urea, thiourea, and sulfonamide moieties and their antimicrobial activity”, Turkish Journal of Chemistry, Vol. 34(1), pp. 57-65. 2010. doi:10.3906/kim-0904-2710.3906/kim-0904-27Search in Google Scholar

[4] World Health Organisation, Global Framework for Development & Stewardship to Combat Antimicrobial Resistance Draft Roadmap. 2017. www.who.int/antimicrobial-resistance/global-action-plan/UpdatedRoadmap-Global-Framework-for-Development-Stewardship-tocombatAMR_2017_11_03.pdf?ua=1Search in Google Scholar

[5] M. M. Ghorab, M. S. Alsaid, M. S. El-Gaby, M. M. Elaasser, Y. M. Nissan, “Antimicrobial and anticancer activity of some novel fluorinated thiourea derivatives carrying sulfonamide moieties: synthesis, biological evaluation and molecular docking”, Chemistry Central Journal, Vol. 11(1), pp. 32, 2017. https://doi.org/10.1186/s13065-017-0258-410.1186/s13065-017-0258-4538391329086809Search in Google Scholar

[6] A. P. Keche, G. D. Hatnapure, R. H. Tale, A. H. Rodge, S. S. Birajdar, V. M. A Kamble, “Novel pyrimidine derivative with aryl urea, thiourea and sulfonamide moieties: synthesis, anti-inflammatory and antimicrobial evaluation.” Bioorganic & Medicinal Chemistry Letters, vol. 22(10), pp. 3445-3448. 2012. https://doi.org/10.1016/j.bmcl.2012.03.09210.1016/j.bmcl.2012.03.09222520258Search in Google Scholar

[7] J. N. Domínguez, C. León, J. Rodrigues, N. G. de Domínguez, J. Gut, P.J. Rosenthal, “Synthesis and antimalarial activity of sulfonamide chalcone derivatives,” Il Farmaco, 60(4), pp. 307-311. 2005. https://doi.org/10.1016/j.farmac.2005.01.00510.1016/j.farmac.2005.01.00515848205Search in Google Scholar

[8] I. R. Ezabadi, C. Camoutsis, P. Zoumpoulakis, A. Geronikaki, M. Soković,, J. Glamočilija, A. Ćirić. “Sulfonamide-1, 2, 4-triazole derivatives as antifungal and antibacterial agents: Synthesis, biological evaluation, lipophilicity, and conformational studies,” Bioorganic & Medicinal Chemistry, Vol.16(3), pp. 1150-1161. 2008. https://doi.org/10.1016/j.bmc.2007.10.08210.1016/j.bmc.2007.10.08218053730Search in Google Scholar

[9] Y. Luo, K. M. Qiu, X. Lu, K. Liu, J. Fu, H. L. Zhu, “Synthesis, biological evaluation, and molecular modeling of cinnamic acyl sulfonamide derivatives as novel antitubulin agents,” Bioorganic & Medicinal Chemistry, Vol. 19(16), pp. 4730-4738. https://doi.org/10.1016/j.bmc.2011.06.08810.1016/j.bmc.2011.06.08821783370Search in Google Scholar

[10] R. S. Keri, M. R. Patil, S. A. Patil, S. A. Budagumpi, “Comprehensive review in current developments of benzothiazole-based molecules in medicinal chemistry,” European Journal of Medicinal. Chemistry, Vol. 89, pp. 207-251, 2015. https://doi.org/10.1016/j.ejmech.2014.10.05910.1016/j.ejmech.2014.10.05925462241Search in Google Scholar

[11] I. C. Chinaka, O. S. Okwudili, D. A. Nkiru, “Chemical Composition, Antioxidant and Antibacterial Properties of Chloroform Fraction of Platycerium Bifurcatum,” Advanced Research in Life Sciences, Vol. 2(1), pp. 1-6, 2018.10.1515/arls-2018-0019Search in Google Scholar

[12] B. A. Adeniyi, O. O. Ayepola, “The phytochemical screening and antimicrobial activity of leaf extracts of Eucalyptus camaldulensis and Eucalyptus torelliana (Myrtaceae),” Research Journal of Medicinal Plant, Vol. 2(1), pp. 34-38. 200810.3923/rjmp.2008.34.38Search in Google Scholar

[13] G. S. Bonjar, “New approaches in screening for antibacterials in plants, “ Asian Journal of Plant Sciences, Vol. 3, pp. 55-60. 2004.10.3923/ajps.2004.55.60Search in Google Scholar

[14] S. Saeed, N. Rashid, P. G. Jones, M. Ali, R. Hussain, “Synthesis, characterization and biological evaluation of some thiourea derivatives bearing benzothiazole moiety as potential antimicrobial and anticancer agents,” European Journal of Medicinal Chemistry, Vol. 45(4), pp. 1323-1331, 2010. https://doi.org/10.1016/j.ejmech.2009.12.01610.1016/j.ejmech.2009.12.01620056520Search in Google Scholar

[15] O. Sköld, “Sulfonamide Resistance: Mechanism and Trends. Drug Resistance Updates,” Vol. 3(3), pp. 155-160, 2000. doi: 10.1054/drup.2000.014610.1054/drup.2000.014611498380Search in Google Scholar

[16] D. Du, Z. Wang, N. R. James, J. E. Voss, E. Klimont, T. Ohene-Agyei, H. Venter, W. Chiu, B. F. Luisi, “Structure of the AcrAB–TolC multidrug efflux pump,” Nature, Vol. 509(7501), pp. 512-515, 2014.doi:10.1038/nature1320510.1038/nature13205436190224747401Search in Google Scholar

[17] X. Z. Li, P. Plésiat, H. Nikaido, “The challenge of efflux-mediated antibiotic resistance in Gram-negative bacteria,” Clinical Microbiology Reviews, Vol. 28(2), pp. 337-418. 2015. doi:10.1128/CMR.00117-14.10.1128/CMR.00117-14440295225788514Search in Google Scholar

eISSN:
2576-6732
Language:
English
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Journal Subjects:
Chemistry, Sustainable and Green Chemistry, Catalysis, other