Synthesis and antibacterial evaluation of novel Schiff base derivatives containing 4(3H)-quinazolinone moiety

References

Alafeefy, A. M., Ashour, A. E., Prasad, O., Sinha, L., Pathak, S., Alasmari, F. A., Rishi, A. K., & Abdel-Aziz, H. A. (2015). Development of certain novel N-(2-(2-(2-oxoindolin-3-ylidene) hydrazinecarbonyl)phenyl)-benzamides and 3-(2-oxoindolin-3-ylideneamino)-2-substituted quinazolin-4(3H)-ones as CFM-1 analogs: Design, synthesis, QSAR analysis and anticancer activity. European Journal of Medicinal Chemistry, 92, 191−201. 10.1016/j.ejmech.2014.12.048Search in Google Scholar PubMed

Bae, S. J., Ha, Y. M., Park, Y. J., Park, J. Y., Song, Y. M., Ha, T. K., Chun, P., Moon, H. R., & Chung, H. Y. (2012). Design, synthesis, and evaluation of (E)-N-substituted benzylidene–aniline derivatives as tyrosinase inhibitors. European Journal of Medicinal Chemistry, 57, 383–390. 10.1016/j.ejmech.2012.09.026.F,Search in Google Scholar PubMed

Bagihalli, G. B., Avaji, P. G., Patil, S. A., & Badami, P. S. (2008). Synthesis, spectral characterization, in vitro antibacterial, antifungal and cytotoxic activities of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases. European Journal of Medicinal Chemistry, 43, 2639–2649. 10.1016/j.ejmech.2008.02.013Search in Google Scholar PubMed

Bharti, S. K., Nath, G., Tilak, R., & Singh, S. K. (2010). Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring. European Journal of Medicinal Chemistry, 45, 651–660. 10.1016/j.ejmech.2009.11.008Search in Google Scholar PubMed

Ceyhan, G., Çelik, C., Uruş, S., Demirtaş, İ., Elmastaş, M., & Tümer, M. (2011). Antioxidant, electrochemical, thermal, antimicrobial and alkane oxidation properties of tridentate Schiff base ligands and their metal complexes. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 81, 184–198. 10.1016/j.saa.2011.05.106Search in Google Scholar PubMed

Giria, R. S., Thakera, H. M., Giordanob, T., Williamsb, J., Rogersb, D., Vasua, K. K., & Sudarsanama, V. (2010). Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-κB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents. Bioorganic & Medicinal Chemistry, 7, 2796−2808. 10.1016/j.bmc.2010.01.007Search in Google Scholar PubMed

Gwaram, N. S., Ali, H. M., Khaledi, H., Abdulla, M. A., Hadi, H. A., Lin, T. K., Ching, C. L., & Ooi, C. L. (2012). Antibacterial evaluation of some Schiff bases derived from 2-acetylpyridine and their metal complexes. Molecules, 17, 5952–5971. 10.3390/molecules17055952Search in Google Scholar PubMed PubMed Central

Kumar, K. S., Ganguly, S., Veerasamy, R., & De Clercq, E. (2010). Synthesis, antiviral activity and cytotoxicity evaluation of Schiff bases of some 2-phenylquinazoline-4(3H)-ones. European Journal of Medicinal Chemistry, 45, 5474−5479. 10.1016/j.ejmech.2010.07.058Search in Google Scholar PubMed PubMed Central

Li, Z. F., Wu, S. L., Bai, X. F., Liu, Y., Lu, J. F., Liu, Y., Xiao, B. G., Lu, X. P., & Fan, L. J. (2011). Genome sequence of the tobacco bacterial wilt pathogen Ralstonia solanacearum, Journal of Bacteriology, 193, 6088–6089. 10.1128/jb.06009-11Search in Google Scholar PubMed PubMed Central

Li, L., Li, Z., Wang, K. L., Zhao, S., Feng, J. M., Li, J. R., Yang, P. W., Liu, Y. X., Wang, L. Z., Li, Y. Q., Shang, H., & Wang, Q. M. (2014). Design, synthesis, and biological activities of aromatic gossypol Schiff base derivatives. Journal of Agricultural and Food Chemistry, 62, 11080−11088. 10.1021/jf504411gSearch in Google Scholar PubMed

Ma, J., Li, P., Li, X. Y., Shi, Q. C., Wan, Z. H., Hu, D. Y., Jin, L. H., & Song, B. A. (2014). Synthesis and antiviral bioactivity of novel 3-((2-((1E,4E)-3-oxo-5-arylpenta-1,4-dien-1-yl)phenoxy) methyl)-4(3H)-quinazolinone derivatives. Journal of Agricultural and Food Chemistry, 62, 8928–8934. 10.1021/jf502162ySearch in Google Scholar PubMed

Mandal, S., Karmakar, T. K., Ghosh, A., Fleck, M., Bandyopadhyay, D. (2011). Synthesis, crystal structure and antibacterial activity of a group of mononuclear manganese(II) Schiff base complexes. Polyhedron, 30, 790–795. 10.1016/j.poly.2010.12.012Search in Google Scholar

Pandeya, S. N., Sriram, D., Nath, G., & DeClercq, E. (1999). Synthesis, antibacterial, antifungal and anti-HIV activities of Schiff and Mannich bases derived from isatin derivatives and N-[4-(4-chlorophenyl)thiazol-2-yl]thiosemicarbazide. European Journal of Pharmaceutical Sciences, 9, 25–31. 10.1016/s0928-0987(99)00038-xSearch in Google Scholar PubMed

Panneerselvam, P., Rather, B. A., Reddy, D. R. S., & Kumar, N. R. (2009). Synthesis and anti-microbial screening of some Schiff bases of 3-amino-6,8-dibromo-2-phenylquinazolin-4(3H)-ones. European Journal of Medicinal Chemistry, 44, 2328−2333. 10.1016/j.ejmech.2008.04.010Search in Google Scholar PubMed

Patel, N. B., Patel, J. C., & Bar, G. G. (2012). In vitro evaluation of the antibacterial and antifungal activity of some new pyrazolyl-quinazolin-4(3H)-one derivatives. Medicinal Chemistry Research, 21, 229–238. 10.1007/s00044-010-9530-zSearch in Google Scholar

Tansir, A., Nahid, N., & Shadma, P. (2008). Synthesis, characterization and antimi-crobial studies of newly developed polymeric Schiff base and its metal-polychelates. Journal of Coordination Chemistry, 61, 1963–1972. 10.1080/00958970701795698Search in Google Scholar

Wang, X., Li, P., Li, Z. L., Yin, J., He, M., Xue, W., Chen, Z. W., & Song, B. A. (2013). Synthesis and bioactivity evaluation of novel arylimines containing a 3-aminoethyl-2-[(p-trifluoromethoxy) anilino]-4(3H)-quinazolinone moiety. Journal of Agricultural and Food Chemistry, 61, 9575−9582. 10.1021/jf403193qSearch in Google Scholar PubMed

Wang, X., Yin, J., Shi, L., Zhang, G. P., & Song, B. A. (2014). Design, synthesis, and antibacterial activity of novel Schiff base derivatives of quinazolin-4(3H)-one. European Journal of Medicinal Chemistry, 77, 65–74. 10.1016/j.ejmech.2014.02.053Search in Google Scholar PubMed

Wu, A. M., Liu, J. H., Herp, A., Sudakevitz, D., & Gilboa-Garber, N. (2012). elative intensities of recognition factors at two combining sites of Ralstonia solanacearum lectin (RSL) for accommodating lFucα1→, dManα1→ and Galβ1→3/4GlcNAc glycotopes. FEBS Letters, 186, 1294–1299. 10.1016/j.febslet.2012.03.024Search in Google Scholar PubMed

Xu, W. M., Han, F. F., He, M., Hu, D. Y., He, J., Yang, S., & Song, B. A. (2012). Inhibition of tobacco bacterial wilt with sulfone derivatives containing an 1,3,4-oxadiazole moiety. Journal of Agricultural and Food Chemistry, 60, 1036−1041. 10.1021/jf203772dSearch in Google Scholar PubMed

Zeng, Z., Yang, H., Peng, Y., & Yang, X. (2015). Synthesis and fungicidal activity of novel 4(3H)-quinazolinone Schiff base derivatives. Chinese Journal of Pesticide Science, 17, 128−135. 10.3969/j.issn.1008-7303.2015.02.02Search in Google Scholar

Zhang, J. A., Pan, M., Zhang, J. Y., Kang, B. S., & Su, C. Y. (2009). Syntheses, structures and bioactivities of cadmium (II) complexes with a tridentate heterocyclic N- and S-ligand. Inorganica Chimica Acta, 362, 3519–3525. 10.1016/j.ica.2009.03.041Search in Google Scholar

Zhu, S., Wang, J., Chandrashekar, G., Smith, E., Liu, X., & Zhang, Y. (2010). Synthesis and evaluation of 4-quinazolinone compounds as potential antimalarial agents. European Journal of Medicinal Chemistry, 45, 3864−3869. 10.1016/j.ejmech.2010.05.040Search in Google Scholar PubMed PubMed Central