Zormapatide
Zormapatide is a gastric inhibitory polypeptide (GIP) receptor agonist peptide. Zormapatide contains 2-methylalanine residues and an N6-[N-(19-carboxynonadecanoyl)-L-γ-glutamyl-L-lysyl] modification. Zormapatide is applicable to the research of diabetes and metabolic diseases.
For research use only. We do not sell to patients.
- CAS No.: 3056608-43-3
- Formula: C209H326N48O58
- Molecular Weight:4439.11
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
As a GIP receptor agonist, Zormapatide activates GIP receptor-related signaling, and is used for in vitro studies of GIP receptor function and glucose metabolism regulation[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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CAS No. 3056608-43-3
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Molecular Weight 4439.11
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Formula C209H326N48O58
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Sequence
Tyr-{Aib}-Glu-Gly-Thr-Phe-Ile-Ser-Asp-Tyr-Ser-Lys-Ala-Leu-Asp-Lys-Ile-His-Gln-Gln-Asp-Phe-Val-Asn-Trp-Leu-Leu-Ala-Gln-Lys-Gly-Lys-{Lys(Lys-Glu-CO-C18-COOH)}
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Sequence Shortening
Y-{Aib}-EGTFISDYSKALDKIHQQDFVNWLLAQKGK-{Lys(Lys-Glu-CO-C18-COOH)}
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Research Protocol for Metabolic Diseases
AMP-activated protein kinase, AMPK, is a conserved cellular energy sensor that responds to reduced cellular energy status and coordinates metabolism by increasing ATP-generating catabolic pathways while suppressing ATP-consuming anabolic processes. In metabolic disease research, the AMPK pathway is experimentally relevant because it regulates hepatic lipid synthesis, fatty acid oxidation, glucose production, skeletal-muscle glucose disposal, mTORC1-linked biosynthesis, autophagy, mitochondrial homeostasis, and whole-body energy balance. The central pathway logic is that energy stress, metformin, exercise-like stimulation, or direct AMPK activators increase AMPKα Thr172 phosphorylation and downstream substrate phosphorylation, including ACC and RAPTOR. Phosphorylation of ACC suppresses lipogenesis and supports fatty acid oxidation, whereas phosphorylation of RAPTOR suppresses mTORC1 signaling and links cellular energy status to growth and protein synthesis control. The pathway is linked
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)