Abstract
A series of benzotriazole derivatives (compounds 1–27) were synthesized, and 24 (compounds 1–5, 9–27) of which were first reported. Their chemical structures were confirmed by means of 1H NMR, IR and elemental analyses, coupled with one selected single crystal structure (compound 1). All the compounds were assayed for antibacterial activities against three Gram positive bacterial strains (Bacillus subtilis, Staphylococcus aureus and Streptococcus faecalis) and three Gram negative bacterial strains (Escherichia coli, Pseudomonas aeruginosa and Enterobacter cloacae) by MTT method. Among the compounds tested, most of them exhibited potent antibacterial activity against the six bacterial strains. Most importantly, compound 3-benzotriazol-1-yl-1-(4-bromo-phenyl)-2-[1,2,4]triazol-1-ylpropan-1-one (19) showed the most favourable antibacterial activity against B. subtilis, S. aureus, S. faecalis, P. aeruginosa, E. coli and E. cloacae with MIC of 1.56 µg/mL, 1.56 µg/mL, 1.56 µg/mL, 3.12 µg/mL, 6.25 µg/mL and 6.25 µg/mL, respectively.
Keywords: Benzotriazoles derivatives, antibacterial activities, crystal structure, structure-activity relationship
References
- 1.Katarzyna K., Zelika N., Justyna Z. Bioorg. Med. Chem. 2004;12:2617. doi: 10.1016/j.bmc.2004.03.022. [DOI] [PubMed] [Google Scholar]
- 2.Li H.-Q., Xu C., Li H.-S., Xiao Z.-P., Shi L., Zhu H.-L. Chem. Med. Chem. 2007;2:1361. doi: 10.1002/cmdc.200700097. [DOI] [PubMed] [Google Scholar]
- 3.Biagi G., Giorgi I., Livi O., Scartoni V., Barili P. L., Calderone V. Il Farmaco. 2001;56:827. doi: 10.1016/S0014-827X(01)01146-6. [DOI] [PubMed] [Google Scholar]
- 4.Scapin G., Patel S. B., Becker J. W., Wang Q., Desponts C., Waddleton D., Skorey K., Cromlish W., Bayly C., Therien M., Gauthier J. Y., Li C.-S., Lau C. K., Ramachandran C., Kennedy B. P., Asante-Appiah E. Biochemistry. 2003;42:11451. doi: 10.1021/bi035098j. [DOI] [PubMed] [Google Scholar]
- 5.Antonio C., Michele P., Gianpiero B., Bernardetta B., Marta M., Roberta L. Il Farmaco. 2004;59:637. doi: 10.1016/j.farmac.2004.03.004. [DOI] [PubMed] [Google Scholar]
- 6.Xu L.-Z., Jian F.-F., Gao H.-R., Chong C.-Y. Chin. J. Chem. 2003;21:1615. doi: 10.1002/cjoc.20030211218. [DOI] [Google Scholar]
- 7.Bushuev M. B., Virovets A. V., Garcia Y., Gieck C., Sheludyakova L. A., Ikorskii V. N., Tremel W., Gütlich P., Lavrenova L. G. Polyhedron. 2002;21:797. doi: 10.1016/S0277-5387(02)00844-6. [DOI] [Google Scholar]
- 8.Touami S. M., Poon C. C., Wender P. A. J. Am. Chem. Soc. 1997;119:7611. doi: 10.1021/ja971042z. [DOI] [Google Scholar]
- 9.Wu C. Y., King K. Y., Kuo C. J., Fang J. M., Wu Y.-T., Ho M. Y., Liao C.-L., Shie J. J., Liang P.-H., Wong C. H. Chem. Biol. 2006;13:261. doi: 10.1016/j.chembiol.2005.12.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Handratta V. D., Vasaitis T. S., Njar V. C. O., Gediya L. K., Kataria R., Chopra P., Newman D., Farquhar R., Guo Z., Qiu Y., Brodie A. M. H. J. Med. Chem. 2005;48:2972. doi: 10.1021/jm040202w. [DOI] [PubMed] [Google Scholar]
- 11.Tomás F., Catalán J., Pērez P., Elguero J. J. Org. Chem. 1994;59:2799. doi: 10.1021/jo00089a026. [DOI] [Google Scholar]
- 12.Wang H., Burda C., Persy G., Wirz J. J. Am. Chem. Soc. 2000;122:5849. doi: 10.1021/ja994464c. [DOI] [Google Scholar]
- 13.Abonia R., Insuastya B., Quirogaa J., Noguerasb M., Meierc H. Mini-reviews in organic chemistry. 2004;1:387. doi: 10.2174/1570193043403037. [DOI] [Google Scholar]
- 14.Zeng W.-L., Bi S., Zhong H., Wan J. Acta Cryst. 2006;E62:O5801. [Google Scholar]
- 15.Zhang S.-S., Wan J., Li C.-L., Li X.-M., Qu B. J. Heterocyclic Chem. 2007;44:75. doi: 10.1002/jhet.5570440112. [DOI] [Google Scholar]
- 16.Wan J., Peng Z.-Z., Li X.-M., Zhang S.-S. Acta Cryst. 2006;E62:O4410. [Google Scholar]
- 17.Bi S., Zeng W. L., Wan J. Acta Cryst. 2007;E63:O1078. [Google Scholar]
- 18.Zeng W. L., Bi S., Wan J. Acta Cryst. 2007;E63:O1076. [Google Scholar]
- 19.Allen F. H., Kennard O., Watson D. G., Brammer L., Orpen A. G., Taylor R. J. Chem. Soc. Perkin Trans. 1987;2:S1. [Google Scholar]
- 20.SADABS . Program for empirical absorption correction of area detector data. Germany: University of Gottingen; 1996. [Google Scholar]
- 21.Sheldrick G. M. SHELXTL, v5 Reference Manual. Madison, Wisconsin, USA: Siemens Analytical X-ray Sysytems, Inc.; 1996. [Google Scholar]
- 22.Wilson A. J. C. International table for X-ray crystallography. Dordrecht: Kluwer Academic Publishers; 1992. pp. 500–502. [Google Scholar]
- 23.Meletiadis J., Meis J. F., Mouton J. W., Donnelly J. P., Verweij P. E. J. Clin. Microbiol. 2000;38:2949. doi: 10.1128/jcm.38.8.2949-2954.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
