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McSweeney et al., 2020)

These modifications make IGF-1 LR3 a commonly studied compound in controlled in-vitro and biochemical research models where sustained peptidereceptor interaction is required

This selective MC1R agonism distinguishes MT-1 from non-selective melanocortin agonists in research applications

It was identified through an extensive medicinal chemistry programme focused on compounds lacking the central Ala-Trp dipeptide of GHRP-1, ultimately yielding a compound with a distinct and highly specific pharmacological profile