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Karthikeyan, M., Prasad, D.J., Boja, P., Bhat, S., Bantwal, S. and Nalilu, S. (2006) Synthesis and biological activity of Schiff and Mannich bases bearing 2,4-dichloro- 5-fluorophenyl moiety. Bioorganic & Medicinal Che- mistry, 14, 7482-7489. doi:10.1016/j.bmc.2006.07.015

has been cited by the following article:

• TITLE: Novel 1,3,4-(thiadiazol-2-ylamino) methyl-5-(pyridin-4-yl)-1,3,4-oxadiazol-2-thiones: synthesis, docking and antimycobacterial testing

  AUTHORS: Trupti S. Chitre, Santosh Panda, Shital M Patil, Aparna S. Chothe, G Vignesh, M. K. Kathiravan

  KEYWORDS: Mannich Base; Oxadiazole; Thiadiazole; Antimycobacterial; Docking

  JOURNAL NAME: Advances in Biological Chemistry, Vol.1 No.2, August 22, 2011

  ABSTRACT: In the present study, a novel series of Mannich bases of 3-substituted 5-(pyridin-4-yl)-1,3, 4-oxadiazol-2-thione derivatives were synthesized. Docking study was performed to rationalize the possible interactions between the synthesized com-pounds and active site of 14DM. The test compounds were screened for antimycobacterial activity using Middlebrook 7H9 medium against M. tuberculosis H37Rv (ATCC 27294) as well as Isoniazid (INH) resistant clinical strain. Among the series 5c and 5a are found to be most potent (susceptible) while the compound 5f did not show activity against M. tuberculosis H37Rv (resistant). The SAR study reveals the importance of substitutions at para position for good activity.