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This compound not only inhibited SARM1s NADase activity effectively but also exhibited a favorable safety profile, making it a strong candidate for further development 233

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Structural focus: As a 16-amino acid peptide, this research compound is significantly smaller and more structurally defined than the 191-amino acid full GH molecule, making it a more tractable research tool for studying specific receptor-ligand interactions and downstream signalling mechanisms in controlled laboratory settings