Rationalization of physicochemical characters of oxazolyl thiosemicarbazone analogs towards multi-drug resistant tuberculosis: A QSAR approach

The emergence of multi-drug resistant (MDR) strains of Mycobacterium tuberculosis and the continuing pandemic of tuberculosis emphasizes the urgent need for the development of new and potent anti-tubercular agents. In an effort to develop new and more effective agents to treat tuberculosis emphasis was focused on quantification of structure–activity relationship of oxazolyl thiosemicarbazone derivatives. The de novo analysis gave insight to some important structural features i.e. nitro group on phenyl ring at R1 position is optimal for the activity and might be responsible for electronic interaction, while phenyl ring at R position interact with the hydrophobic pocket more effectively as compared to unsubstituted or methyl substituted analogs. Hansch approach offered the understanding and parameterization of interactions of the inhibitor with receptor. Similarly QSAR analysis gave some important physicochemical properties, i.e. empirical aromatic index (ARR) and 3D-MoRSE code value of scattering angle at 8Å−1. These two physicochemical properties shall be helpful in the development of more potent analogs.

To develop new and more effective agents to treat tuberculosis emphasis was focused on quantification of structure–activity relationship of oxazolyl thiosemicarbazones derivatives. De novo analysis and Hansch approach offered the understanding and parameterization of interaction of the inhibitor with receptor. Similarly QSAR suggest the role of empirical aromatic index (ARR) and 3D-MoRSE code (3D molecular representation of structure based on electron diffraction code).Figure optionsDownload as PowerPoint slide