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The development of more potent GlyT1 inhibitors was initially inspired by structural modifications of sarcosine, particularly through the introduction of bulky hydrophobic substituents at the nitrogen atom, an approach guided by emerging structural and pharmacological insights into GlyT1 and its relationship to other members of the SLC6 transporter family

According to Komatsu et al

Singh R, Kashyap S, Singh V, Kayastha AM, Mishra H, Saxena PS, Srivastava A, Singh RK (2018) QPRTase modified N-doped carbon quantum dots: a fluorescent bioprobe for selective detection of neurotoxin quinolinic acid in human serum

10.3892/or.2015.3760 160 Kim JungyeonK

Protein S-nitrosylation involves the attachment of the nitrosyl group to the reactive thiol group of a cysteine in a target protein generating an S-nitrosothiol (SNO) in the protein