Mazdutide
Novel dual GLP-1R/GCGR agonist targeting lipid elimination and cellular thermodynamic burn.
Open Mazdutide in the 3D analyzerAnalytical specification
| Empirical formula | C218H332N54O66 |
|---|---|
| Molecular weight | 4610.1 g/mol |
| Isoelectric point (pI) | 6.05 |
| Assay purity (HPLC) | 99.45% |
| Retention time | 5.95 min |
| Peak area / height | 13110 / 1090 |
| Reference batch | MA-2026-K18 |
| Research category | Metabolic & Weight Management |
| Amino-acid sequence | Y-Aib-E-G-T-F-T-S-D-Y-S-I-Aib-L-D-K-I-A-Q-A-F-V-Q-W-L-I-A-G-G-P-S-S-G-A-P-P-P |
Research characteristics
Dual Target
Equal affinity for GLP-1 and Glucagon
Lipolysis
Direct white adipose tissue activation
Energy Balance
Elevates thermogenic research signals
Insulin Sensitivity
Improves skeletal receptor function
Reconstitution
Use the interactive reconstitution calculator to convert vial size (mg), bacteriostatic water volume (ml) and target dose (mcg) into a syringe draw on a standard 100-unit insulin syringe. Open the dosage calculator.
Related metabolic & weight management compounds
Retatrutide (Reta)
Next-generation triple receptor agonist (GLP-1, GIP, GCGR) driving advanced metabolic homeostasis.
Tirzepatide (Tirze)
Dual GIP and GLP-1 receptor agonist targeting glucose homeostasis and body composition dynamics.
Semaglutide
Established GLP-1 receptor agonist mimicking natural incretin hormones with modified clearance curves.
Liraglutide
Acylated human glucagon-like peptide-1 analog designed for clinical metabolic investigation models.
Cagrilintide
Long-acting amylin analogue targeting dual pathways in conjunction with incretin receptor systems.
Orforglipron
Non-peptide oral small-molecule GLP-1 receptor agonist engineered for high bio-availability trials.