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is due to the presence of one weak binding site in MT2 with nanomolar affinity, which has been well-documented and characterized at the molecular level (Krel and Maret 2007b

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Oral and injectable formulations of existing drugs often exhibit poor bioavailability, systemic toxicity, and suboptimal patient adherence due to frequent dosing and adverse effects (e.g., gastrointestinal distress and rashes) (Sattui and Gaffo, 2016)

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It increases energy levels and concentration, may improve metabolism, boosts the immune system, and aids in restful sleep