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Two to four compounds, field by field: identity, United States regulatory status, and what kinds of documents are on file. The table records differences. It does not rank them.

No winner, no score, no recommendation. Counts describe how many documents of each kind Therapept has indexed — not how well a compound works, and not how much has been published overall.

Link to this comparison: /compare?peptides=thymosin-beta-4,bpc-157,tb-500

Side-by-side comparison of Thymosin beta-4, BPC-157, TB-500
Thymosin beta-4BPC-157TB-500
Identity
Class43-residue N-terminally acetylated peptide; the parent molecule of the TB-500 fragmentSynthetic 15-residue peptide corresponding to a partial sequence of human gastric juice protein BPCSynthetic acetylated heptapeptide corresponding to the actin-binding region of thymosin beta-4 (residues 17–23)
Also listed asTimbetasin, Thymosin β4, Tβ4Pentadecapeptide BPC 157, PL-14736, BepecinThymosin beta-4 fragment (LKKTETQ), Ac-LKKTETQ-OH, TB500
Molecular formulaC212H350N56O78SC62H98N16O22C38H68N10O14
Molecular weight4963 g/mol1419.5 g/mol889.0 g/mol
CAS77591-33-4137525-51-0885340-08-9
PubChem CID16132341994195762707662
Sequence length43 residues15 residues7 residues
Data caveatMuch of the wound-healing literature cited in commercial TB-500 material concerns this full-length peptide. Full caveatNone recordedTB-500 is commonly described in vendor material as the Ac-SDKP fragment. Full caveat
United States regulatory status
StatusNo FDA-approved productNo FDA-approved productNo FDA-approved product
FDA applicationNone recordedNone recordedNone recorded
CompoundingNo FDA compounding entry recordedFDA bulk-substance nomination withdrawn; safety concerns remain published.FDA bulk-substance nomination withdrawn; safety concerns remain published.
WADANamed at S2.3 — “Thymosin-β4 and its derivatives e.g. TB-500”, among growth factors and growth factor modulators. Prohibited at all times.Named in Class S0 (Non-Approved Substances). Prohibited at all times; Specified Substance.Named at S2.3 — “Thymosin-β4 and its derivatives e.g. TB-500”. Prohibited at all times; non-Specified.
Research profile
Research purposeNo plain-English profile recordedPreclinical soft-tissue and gut repairPreclinical actin-binding fragment research
Proposed mechanismNo plain-English profile recordedProposed to promote angiogenesis and cell migration through VEGF upregulation and focal-adhesion signalling. Most of the mechanistic work comes from a small number of laboratory groups.Corresponds to the actin-binding region of thymosin beta-4. The proposed mechanism is actin cytoskeletal regulation and cell migration; direct human evidence for the fragment is very limited.
Human evidenceNo plain-English profile recordedPredominantly animal and cell data, plus one small retrospective human case series. Therapept indexes no completed randomised Phase 3 trial.Most wound-healing human data concern full-length thymosin beta-4, a different molecule. Therapept indexes no human interventional trial of the TB-500 fragment itself.
Evidence tierNo plain-English profile recordedPreclinical models; no human efficacy trial indexedPreclinical models; no human efficacy trial indexed
Known safety concernsNo plain-English profile recorded
  • No approved product; FDA published immunogenicity, impurity and characterisation concerns.
  • Named in WADA Class S0 (non-approved substances); prohibited at all times.
  • Human safety data are too limited to characterise a risk profile.
  • No approved product; FDA published aggregation and immunogenicity concerns and stated it had not identified human exposure data for the fragment.
  • Named on the WADA Prohibited List at S2.3 as a thymosin-beta-4 derivative.
  • Human safety of the fragment is essentially uncharacterised.
Evidence gapsNo plain-English profile recorded
  • Independent replication outside the originating laboratory network.
  • Any randomised human trial with clinical endpoints.
  • Oral bioavailability and the fate of the peptide after administration.
  • Any human interventional data for the fragment.
  • Whether the actin-binding fragment reproduces the parent protein's effects.
  • Long-term safety.
Head-to-head evidenceNo plain-English profile recordedNo published head-to-head human trial against TB-500 or any other repair peptide.No published head-to-head trial against BPC-157 or full-length thymosin beta-4.
Named pathwaysNo plain-English profile recordedVEGF signalling · Angiogenesis · Focal adhesion kinase · Fibroblast migrationActin cytoskeleton · Cell migration · Thymosin beta-4 biology
Evidence on file
Records
Human-interventional records000
Human-observational records010
Animal records011
In-vitro records010
Reviews032
Regulatory documents033
Earliest indexedNot recorded20031999
Latest indexedNot recorded20262026

Every identity and regulatory value above is taken from the compound’s record, where its sources are listed. Evidence counts are derived from the published evidence file at build time. A missing class means no document of that kind is indexed — not that none exists.