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The consequences of these modifications are that IGF-1 LR3 retains the pharmacological activity of IGF-1 as an agonist of the IGF-1 receptor, has very low affinity for the insulin-like growth factor-binding proteins (IGFBPs), and has improved metabolic stability resulting in approximately three times greater potency than IGF-1, with a significantly longer half-life of about 2030 hours relative to IGF-1s half-life of about 1215 hours

It does this by working on several hormonal paths at the same time

The popular research peptides used in wellness clinics dont have anything close to tesamorelins evidence base

The peptide calculator handles the math

Simultaneously, DAG is believed to activate protein kinase C (PKC), a family of enzymes implicated in various cellular functions