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Systemic bioavailability with standard oral forms is very low Oral vs

Furthermore, key features include: 99% purity, confirmed by reverse-phase HPLC with controlled impurity profiles 10 mg vial format Lyophilized powder suitable for controlled laboratory reconstitution and measured research use Selective multi-receptor activity Binds melanocortin receptors (MC1R, MC3R, MC4R, MC5R) for comprehensive receptor pharmacology investigations Engineered stability Nle and D-Phe substitutions at positions 4 and 7 enhance enzymatic resistance compared to native -MSH cAMP-dependent signaling Investigated for activation of second-messenger cascades and downstream transcriptional responses Stable freeze-dried formulation Lyophilized for long-term stability at 18 C with minimal degradation For laboratory research use only How is MT-1 synthesized

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The compound was active at very low doses and showed oral bioavailability, crossing the blood-brain barrier after systemic administration

Phys Rev A (1987) 36:43719

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