Synthesis of cinnamoyl tethered indoline derivatives with anti-inflammatory and antioxidant activities

Abstract

Aimed to improve the anti-inflammatory activities of natural antioxidant caffeic acid phenethyl ester, the thirty derivatives of cinnamoyl tethered indoline were synthesized. The structure-activity relationship indicated that the fragments of catechol and 5-Cl-indolinyl were beneficial for the higher dual-activities of antioxidant and anti-inflammation. The most potent compound 4b suppressed the secretions of inflammatory cytokines IL-6 and TNF-α, inhibited inducible nitric oxide synthase (iNOS) expression, upregulated the antioxidant gene HO-1 expression and antioxidant enzyme SOD level, and inhibited oxidative stress marker MDA level. Besides, 4b and its acetate prodrug 4′b could effectively attenuate paw edema more than CAPE. In regard to anti-inflammatory mechanism, 4b suppressed the NF-κB activation associated with phosphorylation of p65 subunit and degradation of IκBα. In summary, this study provided a new anti-inflammatory derivative 4b which was worthy of further research.