Maridebart Cafraglutide
Maridebart cafraglutide (AMG 133), a GIP receptor antagonist and GLP-1 receptor agonist antibody-peptide conjugate
N/A Amino Acids · MW: N/A
Amino Acids
N/A
Molecular Weight
N/A
Half-life
weeks
Research Score
4.5
Studies
7
Storage
Store lyophilized at -20°C, reconstituted at 2-8°C
What is Maridebart Cafraglutide?
Maridebart cafraglutide is a long-acting incretin-based research compound that combines GIP receptor antagonism with GLP-1 receptor agonism in an antibody-conjugate format. It has been studied primarily for obesity and aims to provide durable appetite suppression with infrequent dosing.
Key Benefits & Mechanisms
durable appetite suppression
weight loss
infrequent dosing
dual-pathway incretin modulation
Research Summary
Early clinical studies reported meaningful reductions in body weight, drawing attention to the GIP-antagonist/GLP-1-agonist strategy. Research continues to focus on magnitude of weight loss, tolerability, and practical long-interval dosing.
Related Peptides
RgIA
alpha-Conotoxin RgIA from Conus regius venom
RgIA is a disulfide-rich cone snail peptide that selectively antagonizes the alpha9alpha10 nicotinic acetylcholine receptor. It is used as a research tool in pain and neuroimmune signaling studies and as a pre-clinical analgesic lead.
ExperimentalConantokin-G
Conantokin-G from Conus geographus venom
Conantokin-G is a gamma-carboxyglutamate-rich cone snail peptide that antagonizes NMDA receptor activity. It has been used extensively to study excitatory neurotransmission and seizure biology.
ExperimentalMambalgin-1
Mambalgin-1 from Dendroaspis polylepis venom
Mambalgin-1 is a three-finger snake venom peptide that inhibits acid-sensing ion channels (ASICs), especially ASIC1a and ASIC1b. It is studied as a non-opioid analgesic lead with strong mechanistic value in sensory neuroscience.
ExperimentalHuwentoxin-IV
Huwentoxin-IV from Selenocosmia huwena venom
Huwentoxin-IV is a spider venom peptide that potently targets voltage-gated sodium channels, with strong interest around Nav1.7. It is widely used as a tool compound for ion-channel pharmacology and analgesic discovery.
Experimental