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Vinsova, J., Cermakova, K., Tomeckova, A., Ceckova, M., Jampilek, J., Cermak, P., Kunes, J., Dolezal, M. and Staud, F. (2006) Synthesis and Antimicrobial Evaluation of New 2-Substituted 5,7-Di-Tert-Butylbenzoxazoles. Bioorganic & Medicinal Chemistry, 14, 5850-5865.
http://dx.doi.org/10.1016/j.bmc.2006.05.030

has been cited by the following article:

• TITLE: Design, Synthesis and Biological Evaluation of Novel Antitubercular Agents by Combining Pyrazoline and Benzoxazole Pharmacophores

  AUTHORS: Hemal M. Soni, Popatbhai K. Patel, Mahesh T. Chhabria, Ashish K. Patel, Dharmraj N. Rana, Pathik S. Brahmkshatriya

  KEYWORDS: Antitubercular, Benzoxazole, Pyrazoline, Pharmacophore, Microplate Alamar Blue Assay

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.3, September 19, 2016

  ABSTRACT: Various recent reports on Tuberculosis have alarmed an increase in the patient class and subsequent death rates across the globe. Over and above the spread of more dangerous and fatal forms of tuberculosis like MDR-TB i.e. multiple-drug resistance tuberculosis, XDR-TB i.e. extensively-drug resistance tuberculosis & TDR-TB i.e. total-drug resistance tuberculosis has forwarded an urgent need to discover novel antitubercular agents. The current work is aimed at combining two previously well-known pharmacophores (pyrazoline and benzoxazole nucleus) in order to design and synthesize a series of novel benzoxazole-based pyrazoline derivatives. The synthesized target compounds were structurally confirmed by LCMS, 1H-NMR and 13C-NMR analysis. The target compounds were In vitro evaluated against M. tuberculosis H37Rv strain, multidrug-resistant TB (MDR-TB) and extensively drug-resistant TB (XDR-TB) strains. The In vitro screening results depicted that majority of the target compounds displayed potent activity with MIC in a range of ~0.8 to 6.25 μg/mL. Many compounds were found to be more potent than isoniazid against MDR-TB with MIC value 3.12 μg/mL and XDR-TB with MIC value 12.5 μg/mL. Cytotoxicity assay of these active compounds on VERO cell lines also displayed good selectivity index.