Dual receptor activity
LY3298176 activated GIP and GLP-1 signaling; early clinical cohorts assessed metabolic endpoints and reported gastrointestinal adverse events.
Coskun et al., 2018 →Lipidated incretin peptide
Tirzepatide is investigated as a dual GIP and GLP-1 receptor agonist in metabolic research, including translational and clinical studies.

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Mixed · Study formulation · Cell/animal experiments and phase 1 human cohorts
LY3298176 activated GIP and GLP-1 signaling; early clinical cohorts assessed metabolic endpoints and reported gastrointestinal adverse events.
Coskun et al., 2018 →Literature findings; refer to the model and formulation studied.
Tirzepatide — lipidated incretin peptide. The literature identity must be matched to the documented chemical form and composition of the supplied material.
Cell assays characterized GIP and GLP-1 receptor activation by LY3298176. Mouse experiments examined glucose-dependent insulin secretion and metabolic profiles. Early human work included healthy participants and people with type 2 diabetes, who should not be merged into one population.
Cell/animal experiments and phase 1 human cohorts
LY3298176 activated GIP and GLP-1 signaling; early clinical cohorts assessed metabolic endpoints and reported gastrointestinal adverse events.
Evidence concerns the studied material and model, not the supplied BLOPEP batch.
Coskun T, Sloop KW, Loghin C, Alsina-Fernandez J, Urva S, Bokvist KB, Cui X, Briere DA, Cabrera O, Roell WC, Kuchibhotla U, Moyers JS, Benson CT, Gimeno RE, D'Alessio DA, Haupt A · 2018 · Molecular metabolism
DOI: 10.1016/j.molmet.2018.09.009Nominal variant content; analytical results belong to the documented batch.
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Batch results have not yet been published on this page.
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