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(December 1996)

[3] It has a short half-life of approximately 30 minutes

Two key structural features distinguish it from other GHRPs: (1) incorporation of an -aminoisobutyric residue (Aib) at position 1 replacing the histidine of classical GHRPs, stabilising the -turn conformation required for receptor activation, (2) presence of a D-2-naphthyl-alanine (D-2-Nal) at position 3 replacing the D-isomer tryptophan, increasing GHS-R1a selectivity over related receptors

By outsourcing that task, Lilly might give up some margin, but it enables them to scale up and down production significantly faster