Thymosin-β4 Fragment 1-4
Healing & repair Research only Animal studies
Also called Ac-SDKP, Seraspenide
The first four amino acids of thymosin-β4, which the body clips off naturally. This fragment carries much of the parent peptide's anti-inflammatory and anti-scarring activity. In animal models it reduced fibrosis in the heart, kidney and lung. ACE breaks it down, so ACE-inhibitor drugs raise its levels.
Evidence at a glance
- Evidence
- Animal studies — Not yet studied in people
- Status
- Research compound only
- Dosing
- No human study has set a dose
Animal only. It is broken down by ACE, so its levels are already altered by common blood pressure drugs.
What studies report
- Reduced fibrosis in heart, kidney and lung models
- Anti-inflammatory effects without the actin-binding activity of the full peptide
How it works
The first four residues of thymosin-β4, cleaved off naturally. This fragment blocks NF-κB activation and carries most of the parent peptide's anti-scarring and anti-inflammatory effect. ACE breaks it down, so ACE inhibitors raise its levels.
Where it acts
Joints & cartilageThe library groups this compound under Healing & repair. The diagram shows that target, not every tissue it reaches.
Illustrated

AI-generated subject illustration; not a depiction of the compound or evidence of its effects.
Why people take it
Reasons people seek it out — not a list of proven effects.
Status: Animal and cell research only.
- Route
- Subcutaneous injection, from reconstituted lyophilised powder
- Sequence
- Ac-Ser-Asp-Lys-Pro
- Formula
- C20H33N5O9
- Molecular weight
- 487.5 g/mol
- CAS
- 127103-11-1
- Available as
- 10 mg
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Educational information only. Nothing here is medical advice, a dosing protocol, or a recommendation to use any compound. Most entries describe substances not approved for human use. Talk to a licensed clinician before acting on anything you read here. How to read these entries.