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Compounds 6a and 6b (with pyrimidine moiety, amide linkage, and phenolic substrate) might be potent bacterial flavohemoglobin (flavoHB) inhibitors and they could set a promising starting point for future design of antibacterial agents.

rsc advances

Synthesis, characterization,<i>in silico</i>molecular docking, and antibacterial activities of some new nitrogen-heterocyclic analogues based on a<i>p</i>-phenolic unit

Synthesis, characterization,in silicomolecular docking, and antibacterial activities of some new nitrogen-heterocyclic analogues based on ap-phenolic unit