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Nevertheless, existing literature concerning the connection between the structural characteristics and bioactivity are sporadic and this calls for comprehensive SAR analysis to help derive ideal peptide structures with respect to their future therapeutic use

Simultaneously, through its sulfhydryl group binding with free radicals in the body, GSH can directly reduce free radicals into acidic substances, thereby accelerating their excretion and counteracting the damage caused by free radicals to vital organs

Modifying specific cysteines of the electrophile-sensing human Keap1 protein is insufficient to disrupt binding to the Nrf2 domain Neh2

A steady increase in the frequency of drug-resistant tuberculosis cases has significantly complicated the therapeutic landscape

The binding selectivity of CHE toward G-quadruplexes is confirmed by both experimental and theoretical determination (Terenzi et al., 2019)

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