Triple G 20 mg (Retatrutide) – Reagent in vial
Contemporary biochemistry and molecular pharmacology continuously strive to discover substances that could comprehensively mimic the body’s natural regulatory processes. Triple G 20 mg, chemically identified as Retatrutide (LY3437943), represents a pinnacle achievement in this field, defining a new category in peptide engineering. It is an advanced, synthetic incretin analog that transcends traditional mono- and dual-agonist paradigms, offering researchers a unique mechanism of triple agonism.
As a single, precisely designed peptide molecule, Retatrutide simultaneously interacts with three key signaling pathways:
- Glucagon-Like Peptide-1 Receptor (GLP-1),
- Glucose-Dependent Insulinotropic Polypeptide Receptor (GIP),
- Glucagon Receptor (GCG).
This innovative structure makes Triple G a reference material of fundamental importance for laboratories focusing on endocrinology and metabolic diseases. This substance enables scientists to explore the complex synergy between the insulinotropic effect of incretins and the energetic influence of glucagon, which has previously been difficult to achieve using separate ligands.
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