Drug intelligence / Profile preview

N-acetyl lysyltyrosylcysteine amide

Development stage
Preclinical
Lead developer
ReNeuroGen
Modality
Peptides, Small Molecules
Administration
Subcutaneous
01

Overview

N-acetyl lysyltyrosylcysteine amide (KYC) is a tripeptide-based myeloperoxidase (MPO) inhibitor and redox-modulating agent under development for the treatment of inflammatory and oxidative stress-driven conditions, including diabetic cardiomyopathy and cardiovascular diseases. KYC works by inhibiting the enzymatic activity of MPO, thereby reducing the production of hypochlorous acid and other reactive oxygen species that contribute to tissue damage and fibrosis. In preclinical models of type 2 diabetes, KYC has been shown to improve cardiac function, reduce myocardial fibrosis, and modulate the immune system by expanding CD4+CD25+Foxp3+ regulatory T cells (Tregs) while dampening systemic inflammation. Additionally, KYC treatment has been associated with the activation of regulatory and antioxidative defense pathways, including the Nrf2 pathway. The drug is being developed by ReNeuroGen in collaboration with academic institutions such as the Medical College of Wisconsin.

Other names
N-acetyl-L-lysyl-L-tyrosyl-L-cysteine amideN-acetyl-Lys-Tyr-Cys-NH2N-acetyl-Lys-Tyr-Cys-NH-2N-acetyl-Lys-Tyr-Cys-NH 2
02

Targets

MPO (Myeloperoxidase)

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