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Computational, crystallographic studies, cytotoxicity and anti-tubercular activity of substituted 7-methoxy-indolizine analogues

Fig 8

Intermolecular interactions of docked 7-methoxy-indolizine analogues 5a–5j at the active site of the enoyl-[acyl-carrier] protein-reductase enzyme.

Fig 8

doi: https://doi.org/10.1371/journal.pone.0217270.g008