CAS 2023788-19-2 · Metabolic Research
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⚠ RESEARCH USE ONLY
This product is sold strictly for in vitro laboratory research use only. Not for human or animal consumption, diagnostic use, or therapeutic application. Purchasers must be qualified researchers or authorized purchasers for a research institution.
Tirzepatide is a synthetic 39-amino-acid peptide engineered as a dual agonist targeting both the glucose-dependent insulinotropic polypeptide receptor (GIPR) and the glucagon-like peptide-1 receptor (GLP-1R). Its balanced activity at both incretin receptors distinguishes it from earlier GLP-1 mono-agonists and positions it as a widely-studied research tool in metabolic biology.
In research models, tirzepatide has been examined for glucose-dependent insulin secretion, appetite signaling, gastric-emptying kinetics, and combined incretin-pathway effects on body composition and glycemic control.
Reference: Coskun T. et al. (2018), Molecular Metabolism, 18, 3-14.
Tirzepatide emerged from research programs at Eli Lilly investigating dual-incretin receptor activation as a strategy beyond single-receptor GLP-1 agonism. Preclinical work characterized the molecule as a GIPR-biased dual agonist with a fatty-acid-modified backbone enabling once-weekly dosing profiles. It was first described in the peer-reviewed literature in 2018 and subsequently studied across a range of preclinical metabolic models.
Reference: Frias J. P. et al. (2018), The Lancet, 392(10160), 2180-2193.
CAS #: 2023788-19-2
Molecular Formula: C225H348N48O68
Molecular Weight: 4,813.53 g/mol
PubChem CID: 156588324
Tirzepatide has been examined across preclinical rodent, non-human primate, and human research settings. Reported findings describe dual activation of GIPR and GLP-1R with GIPR-biased signaling, glucose-dependent insulin secretion, delayed gastric emptying, appetite regulation via central pathways, and dose-dependent effects on body weight and glycemic parameters.
Key Areas of Research:
Together, these observations position tirzepatide as a widely-used research tool for studying dual-incretin receptor activation across metabolic and body-composition biology.
References: Jastreboff A. M. et al. (2022), NEJM, 387(3), 205-216; Rosenstock J. et al. (2021), The Lancet, 398(10295), 143-155.
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