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Technical Data Sheet

Tirzepatide

Also Known As: LY3298176, Tirzepatide peptide, GIP GLP-1 dual agonist, Eli Lilly dual agonist, Twin incretin, Twincretin, GLP-1 GIP tirzepatide, Mounjaro injection, Zepbound injection, Tirzepatide LY3298176, Dual incretin obesity drug, Tirzapatide, Tirzepetide, GIP/GLP-1, twincretin, tirz, tzp

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Evidence TierApproved Drug
CategoryWeight Loss & Metabolism
ClassDual GIP/GLP-1 receptor co-agonist (twincretin); synthetic 39-residue peptide with C18 fatty diacid for albumin binding
Molecular TargetGIPR (GIP receptor) + GLP-1R (GLP-1 receptor); dual incretin axis activation; pancreatic insulin secretion and hypothalamic appetite suppression
Sequence39-aa acylated peptide (C20 diacid)
Molecular Weight~4814 g/mol
CAS2023788-19-2
ParentIncretin dual agonist
MechanismIt is a dual GIP and GLP-1 receptor agonist. It dramatically slows gastric emptying and sensitizes the body to insulin, resulting in profound appetite suppression and record-breaking weight loss in trials.
Studied ForType 2 diabetes management, Chronic weight management / obesity, Obstructive sleep apnea in obesity (FDA approved 2024), Non-alcoholic fatty liver disease (NAFLD/MASH), Cardiovascular risk reduction, HbA1c lowering, Body weight reduction superior to semaglutide, Insulin resistance, Metabolic syndrome, Polycystic ovary syndrome, Kidney disease in diabetes, Heart failure with obesity, Appetite suppression dual pathway, Lean mass preservation, weight loss, diabetes, fat loss, appetite suppression, obesity, metabolic syndrome, insulin sensitivity, A1C reduction
Administration RouteInjection Only
Formlyophilized (research) or pen/vial
Diluentbacteriostatic water
Storage TemperatureRefrigerate 36-46°F
Light SensitiveYes
Freeze / Thawavoid
Reconstituted Shelf Life28 Days
Handling NotesAvoid freeze-thaw, heat, and shaking.
RegulatoryFDA-approved: Mounjaro (T2D, 2022); Zepbound (chronic weight management, 2023); Zepbound approved for moderate-to-severe obstructive sleep apnea in adults with obesity (Dec 2024). Compounded versions are not FDA-evaluated. Not on the WADA 2026 Prohibited List; tirzepatide was added to the WADA Monitoring Program effective 1 January 2026 (monitored, not sanctioned).
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Research Use Only

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