Design and synthesis optimization of novel diimide indoles derivatives for ameliorating acute lung injury through modulation of NF-KB signaling pathway

Acute lung injury (ALI) is a common respiratory disease caused by local or systemic inflammatory reaction. Based on the natural 7-chain diaryl anti-inflammatory framework, a series of diimide indoles derivatives were designed by combining curcumin and indole in this study. The synthesis of diimide compounds was extended using dichloromethane (DCM) as solvent and 1,1 '-carbonyldiimidazole (CDI) and sodium hydride (NaH) as double activators, and a total of 40 diimide-indole derivatives were obtained. The results of in vitro anti-inflammatory activity showed that most compounds could inhibit the production of interleukin-6 (IL-6) better than curcu-min and indomethacin. Among the compounds, the IC50 of compound 11f on IL-6 reached 1.05 mu M with no obvious cytotoxic side effects. Mechanistically, compound 11f could block the expression of NF-KB P65 phos-phorylation, and nuclear translocation of P65. The acute toxicity tests in-vivo also showed no obvious toxicity in mice after the intragastric administration of 1000 mg/kg. In addition, the compound 11f could significantly inhibit the LPS-induced inflammatory response in mice and reduce the number of neutrophils and wet/dry lung weight ratio, thereby alleviating ALI. These results indicated that the novel diimide indoles were promising anti-inflammatory agents for the treatment of ALI.

Automated summary

A series of diimide indole derivatives were designed and synthesized to treat acute lung injury. Some of these compounds showed good anti-inflammatory activity and were able to alleviate lung damage. These findings suggest that these novel diimide indoles have potential value for the treatment of acute lung injury.