Synthetic heptapeptide
Selank
Thr-Lys-Pro-Arg-Pro-Gly-Pro
Not FDA-approved in the U.S.A synthetic peptide studied in neurobehavioral and stress-response research, with limited high-quality clinical evidence available in U.S. regulatory sources.
FULL RESEARCH GRAPHIC
Selank research overview
A dedicated overview of Selank, stress-response and neurotransmission research, and the 10 mg vial.
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RESEARCH SIGNAL MAP
04 ACTIVE FIELDSEVIDENCE READOUT
Not FDA-approved in the U.S.Research findings are not the same as proof of an anxiolytic or nootropic treatment, particularly when product quality and route vary.
BOUNDARY CHECK
CONTEXT REQUIREDFDA says it lacks important information needed to understand the safety of compounded Selank acetate administered to humans.
SUBMITTED LAB DOCUMENTS
Test results
Reports may describe other strengths or blends. Match the labeled amount, composition, and exact lot to your vial. A report for another strength does not verify your vial. Each record identifies whether an exact lot was supplied.
VIAL REFERENCE
3 mL mixing math & dosing context
Every number is labeled by evidence level. The 3 mL reference calculates concentration and U-100 volume; it does not prove solvent compatibility, sterility, stability, or suitability for injection.
10 mg vial
Change the liquid. See the amount.
Calculation only: vial amount ÷ liquid volume × draw volume. It does not determine what dose to use or confirm product compatibility.
3.0 mL BAC-water workflow
- First confirm that bacteriostatic water and a 3.0 mL final volume are compatible with the exact product and vial capacity.
- Clean both vial stoppers with alcohol and allow them to dry.
- Add the 3.0 mL slowly down the inside wall instead of directing pressure onto the powder.
- Gently roll or swirl until dissolved; do not shake.
- Use product-specific refrigeration and discard guidance. If none exists, do not invent a beyond-use date.
No standardized U.S. human dose
Selank is not FDA-approved in the United States, and FDA says important information needed to understand the safety of compounded Selank acetate in humans is lacking.
FDA — compounding safety risks ↗U-100 means 100 units = 1.0 mL. Any table result above 100 units exceeds one standard 1 mL U-100 syringe.