MOTS-c cross-reactivity with other GPCR signaling: pharmacological profiling
Kim KH, Sripada L, Zhang K, et al.
Journal of Pharmacology and Experimental Therapeutics, 2024
Key finding
MOTS-c showed high selectivity; only significant interactions were with formyl peptide receptors (FPR1, IC50=420nM) and CXCR4 (IC50=890nM).
Summary
Comprehensive receptor profiling of MOTS-c against >150 human GPCRs, nuclear receptors, and ion channels to define specificity and potential off-target effects.
Read the study
The full citation, abstract, and (when available) the full text can be accessed on PubMed. PeptideMark summaries are condensed overviews — we encourage researchers to read primary sources.
View on PubMedRelated compound
More research on MOTS-c
Human pilot study: MOTS-c supplementation improves insulin sensitivity
Journal of Clinical Endocrinology & Metabolism · 2025 · Human Pilot
Mitochondrial-derived peptide MOTS-c mediates beneficial metabolic effects of exercise
Cell Reports · 2024 · Animal Study
MOTS-c analog development and pharmacokinetics: oral bioavailability enhancement
Biochemical Pharmacology · 2024 · Animal Study
MOTS-c enhances glucose uptake through AMPK-independent mechanisms in muscle
Metabolism: Clinical & Experimental · 2024 · Animal Study
MOTS-c and liver metabolism: effects on hepatic glucose production and lipid metabolism
Journal of Hepatology · 2024 · Animal Study