DOI: 10.1039/d6md00729e ISSN: 2632-8682

DprE1 inhibitors in tuberculosis: integrating structural binding determinants, IC 50 –MIC translation, and physicochemical constraints for rational drug design

Fady H. Fayek, Mai H. A. Mousa, Mona F. Said, Hanan H. Georgey, Nagwa M. Abdel Gawad

Decaprenylphosphoryl-β-

d
-ribose 2′-epimerase (DprE1) has emerged as one of the most validated and clinically relevant targets for antitubercular drug discovery.

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