FGL (FG Loop Peptide) Dosage Calculator
FGL is a synthetic pentadecapeptide corresponding to residues E681-A695 of the second fibronectin type III homology module of the neural cell adhesion molecule (NCAM).
1mcg · 5x/week
Summary: Add 2mL BAC water to your 5mg vial. Draw to < 0.1 units on a U-100 syringe for a 1mcg dose. This vial will last 5000 doses.
Cycle Planner
FGL (FG Loop Peptide) Pharmacokinetics
Pharmacokinetics — Active Dose Over Time
t½ = ~4-6 hours (subcutaneous administration)Disclaimer: This curve is a simplified first-order exponential decay model. Actual pharmacokinetics vary based on injection site, individual metabolism, body composition, and other factors. Half-life values are approximate and based on available preclinical and clinical literature. Many research peptides lack formal human pharmacokinetic studies. This is for educational purposes only — not medical advice.
FGL (FG Loop Peptide) Dosing Protocol
| Level | Dose / Injection | Frequency |
|---|---|---|
| Beginner | 1mg | 5x/week |
| Moderate | 1.5mg | 5x/week |
| Aggressive | 2mg | 5x/week |
Note: FGL is a 15-amino-acid synthetic peptide derived from the second fibronectin type III module of the neural cell adhesion molecule (NCAM). The active clinical form is FGL(L), a dimerized version consisting of two FGL monomers linked together, which provides better blood-brain barrier penetration. A Phase I clinical trial has confirmed tolerability and safety of intranasal FGL(L) in healthy volunteers at doses up to 200 mg. Always source the dimerized FGL(L) form rather than the monomer for optimal CNS activity.
About FGL (FG Loop Peptide)
FGL is a synthetic pentadecapeptide corresponding to residues E681-A695 of the second fibronectin type III homology module of the neural cell adhesion molecule (NCAM). It was designed to mimic the specific region of NCAM that binds and activates fibroblast growth factor receptor 1 (FGFR1), making it a targeted FGFR1 agonist with potent neurotrophic and neuroprotective properties. Research on FGL spans over two decades and includes both preclinical and early clinical work. In rodent models of ischemic stroke, a single suboccipital injection of FGL given 24 hours before induced global ischemia significantly protected hippocampal CA1 neurons from death. The peptide also preserves metabolic function and presynaptic activity in hippocampal slice cultures exposed to oxygen-glucose deprivation, whether applied before or after the insult. FGL's cognitive benefits are among its most compelling features. Intracerebroventricular administration immediately after training in fear conditioning or water maze tasks produced long-lasting memory improvements persisting up to one month in rats. The peptide enhances long-term potentiation (LTP) in the dentate gyrus of freely moving animals, with effects lasting up to 24 hours — the first demonstration that mimicking the NCAM-FGFR interaction promotes hippocampal synaptic plasticity in vivo. Beyond neuroprotection and memory, FGL mobilizes endogenous neural stem cells from the subventricular zone and hippocampus after stroke, promoting remyelination and modulating neuroinflammation through microglial regulation. A Phase I clinical trial using intranasal FGL(L) at doses up to 200 mg in healthy volunteers confirmed tolerability with dose-proportional systemic exposure and detectable brain penetration.