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Therefore, our compounds significantly lower IC 50 , coupled with its competitive inhibition profile, suggests it could be a promising GSTP1 inhibitor with both higher potency and a potentially safer therapeutic profile
NPJ Parkinsons Dis 8(1):135 Bnit P et al (2022) Succinate dehydrogenase, succinate, and superoxides: a genetic, epigenetic, metabolic, environmental explosive crossroad
By using LAT1-4F2hc as the model, we found that the LAAM GSH-CQDs could bind to the LAT1 mainly through hydrogen bonds formed between the amino acid groups on LAAM GSH-CQDs and the Glu457, Glu78, Asn242 and Leu238 residues in LAT1 with a docking energy of 8.80 kcal mol 1 (Supplementary Fig
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