What Is TB-500 Frag? Dosage, Half-Life & How to Track It
Also known as: Ac-SDKP · TB4-Frag · Goralatide · Thymosin Beta-4 N-Terminal Fragment
TB-500 Frag is sold as a smaller, cheaper alternative to full TB-500 — but it is not simply a truncated version of the same molecule. What ships under this name is almost always Ac-SDKP, the natural four-amino-acid fragment cleaved from the N-terminal end of thymosin beta-4, which works through a completely different mechanism than TB-500’s actin-binding domain. Its plasma half-life is extremely short, on the order of 5 minutes, and there is essentially no validated human self-dosing data — community protocols describe 100–300 mcg subcutaneously daily, unvalidated. Educational information only.
What TB-500 Frag actually is (and why the name is misleading)
TB-500 Frag is marketed as a fragment of TB-500 (thymosin beta-4) — implying a smaller piece of the same healing molecule at a lower price. What is actually being sold under that name, in nearly every case, is Ac-SDKP (N-acetyl-Ser-Asp-Lys-Pro), also known by the generic name goralatide. It is a real, well-characterized natural peptide — but it is the fragment cleaved from the N-terminal end of thymosin beta-4, structurally and functionally unrelated to the actin-binding domain that gives full-length TB-500 its cell-migration effect.
That distinction matters because the two compounds do different jobs. TB-500 mobilizes repair cells throughout the body by binding G-actin. Ac-SDKP does not touch actin at all — its best-documented roles are keeping hematopoietic stem cells in a quiescent, non-dividing state, and acting as an antifibrotic signal that limits excess collagen deposition in the heart, kidney, and lung. Buying “TB-500 Frag” expecting TB-500’s wound-healing effect at a discount is buying the wrong peptide for that goal.
Ac-SDKP has one more genuinely notable property: it is the natural substrate of ACE (angiotensin-converting enzyme), the same enzyme ACE-inhibitor blood pressure drugs block. That is not a coincidence — part of why ACE inhibitors show antifibrotic benefits in the heart and kidney is thought to run through the resulting 5–10× rise in circulating Ac-SDKP levels, since ACE is what normally destroys it. This gives Ac-SDKP an unusually strong mechanistic backing for a research peptide, even though it was never developed as a self-administered injectable.
Typical dosing & reconstitution
Because Ac-SDKP is sold through the same research-peptide channels as BPC-157 and TB-500, it typically ships the same way: lyophilized powder reconstituted with bacteriostatic water. Community-reported protocols describe 100–300 mcg subcutaneously once daily, but this is worth being direct about — there is no clinical precedent for that route or schedule. Published Ac-SDKP research is dominated by continuous IV infusion in animal and small human cardioprotection studies, not a daily subcutaneous bolus.
| Vial | BAC water | Concentration | 1 unit (U-100) ≈ |
|---|---|---|---|
| 2 mg | 2 mL | 1.0 mg/mL | 10 mcg |
| 5 mg | 3 mL | 1.67 mg/mL | 16.7 mcg |
At 1.0 mg/mL, a 200 mcg dose is 20 units on a standard U-100 insulin syringe. The reconstitution math is identical to any other lyophilized peptide — what is genuinely uncertain is whether the once-daily schedule reflects the compound’s actual pharmacology, given its 5-minute plasma half-life.
Half-life & what it means for frequency
Ac-SDKP clears from plasma extremely fast — roughly 5 minutes — because ACE degrades it almost as quickly as it appears, the same relationship that makes it accumulate when ACE is pharmacologically blocked. A once-daily subcutaneous injection produces a brief spike, not a sustained elevation, which is a mismatch with how the compound’s best-documented effects were actually studied — using continuous exposure, not a single daily peak.
This is the honest caveat that gets lost in “TB-500 Frag” marketing: a 5-minute half-life dosed once a day means blood levels are only meaningfully elevated for a small fraction of each 24-hour period. Whether that intermittent exposure produces any of the antifibrotic or stem-cell effects seen in continuous-infusion research is genuinely unknown.
What to track & common side effects
There is no established human side-effect profile for self-administered Ac-SDKP at research-peptide doses — the compound’s human data comes from IV infusion studies in specific clinical contexts, not from daily subcutaneous self-dosing. Reported issues in the research-peptide community mirror any small injectable peptide: injection-site irritation and occasional lightheadedness.
Given how thin the dosing evidence is, the useful thing to track is the plain record: dose, timing, and site, logged consistently enough that if anything changes — good or bad — you have an actual timeline to look at rather than a memory of “a few weeks ago.”
How to track TB-500 Frag in Stackeddd
Log each TB-500 Frag dose and site the same way you would any other research peptide — with human self-dosing data this thin, your own record is effectively the only data you have on what you took and when. Get the reconstitution math right up front so a “200 mcg” dose is actually 200 mcg.
Model it yourself · free, no account
Reconstitution Calculator
Model it yourself: enter your vial size and BAC water and the Peptides tab returns concentration and exact units for any dose — the same math built into the Stackeddd app, regardless of how thin the underlying dosing evidence is.
Related compounds
Related reading: What peptides can you mix in the same syringe? · Peptide reconstitution math: how much BAC water to add
Frequently asked questions
Is TB-500 Frag the same as TB-500?
No. What is sold as “TB-500 Frag” is almost always Ac-SDKP, the N-terminal fragment of thymosin beta-4 — a different molecule from the actin-binding C-terminal region that gives full TB-500 its systemic healing effect. They work through unrelated mechanisms.
What is Ac-SDKP used for?
Ac-SDKP is studied for keeping hematopoietic stem cells in a quiescent state and for antifibrotic effects that limit collagen buildup in the heart, kidney, and lung. It is also the natural substrate of ACE, the enzyme targeted by ACE-inhibitor blood pressure drugs.
What is the half-life of TB-500 Frag (Ac-SDKP)?
Roughly 5 minutes in plasma, due to rapid degradation by ACE. That is far shorter than TB-500’s effective activity window, and it means a once-daily injection produces only a brief spike rather than sustained exposure.
Should you buy TB-500 Frag instead of TB-500 for injury recovery?
Not on the assumption that it is a cheaper version of the same effect. TB-500’s healing effect comes from actin-binding cell mobilization that Ac-SDKP does not share — if systemic tissue repair is the goal, TB-500 itself is the peptide with that mechanism.
This is educational information, not medical advice. Doses and protocols above reflect published references and community practice — protocol decisions belong with your prescribing physician. Generic names used throughout. How this reference is built & how the AI is tested →
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