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Another critical, and often underappreciated, consideration is the pharmacological selectivity of GlyT1 inhibitors within the broader SLC6 family, which comprises closely related transporters such as GlyT2 (SLC6A5) and PROT (SLC6A7), as well as several monoamine transporters (e.g., DAT, SERT, and NET) (de Carvalho et al

Protective effects of caffeic acid phenethyl ester against experimental allergic encephalomyelitis-induced oxidative stress in rats

Retracted] ellagic acid: A review on its natural sources, chemical stability, and therapeutic potential

Furthermore, ScGrx8, which has an alanine residue at the same position (Fig

10.1039/d3tb01489d 21 BoucherR

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