Simple isatin derivatives as free radical scavengers: Synthesis, biological evaluation and structure-activity relationship

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Abstract

To develop more potent small molecules with enhanced free radical scavenger properties, a series of N-substituted isatin derivatives was synthesized, and the cytoprotective effect on the apoptosis of PC12 cells induced by H2O2was screened. All these compounds were found to be active, and N -ethyl isatin was found with the most potent activity of 69.7% protective effect on PC12 cells. Structure-activity relationship analyses showed the bioactivity of N -alkyl isatins decline as the increasing of the chain of the alkyl group, furthermore odd-even effect was found in the activity, which is interesting for further investigation. © 2010 Chen et al.

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Chen, G., Wang, Y., Hao, X., Mu, S., & Sun, Q. (2011). Simple isatin derivatives as free radical scavengers: Synthesis, biological evaluation and structure-activity relationship. Chemistry Central Journal, 5(1). https://doi.org/10.1186/1752-153X-5-37

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