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This central mechanism contrasts fundamentally with PDE5 inhibitors, which work by inhibiting phosphodiesterase-5 enzyme in genital smooth muscle - a purely peripheral vascular mechanism that doesn't directly address desire or motivation

The modification retained full MC4R agonist activity while improving the compound's selectivity profile and facilitating its development as a focused pro-sexual therapeutic rather than a pan-melanocortin agonist [9]

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