Neuropeptides
Semax
A synthetic heptapeptide derived from an ACTH fragment.
Early human evidence
- Evidence
- Early clinical
- Status
- Published
Topic authority hub
Stroke, nerve-injury, stress, mitochondrial, and cellular models organized without turning preclinical signals into human claims.
Neuroprotection is an evidence-sensitive topic because animal injury models, cell survival assays, and human neurological outcomes do not answer the same question.
This hub brings together Semax, Selank, Pinealon, Cortagen, and SS-31 pages while keeping study type and species visible.
Neuropeptides
A synthetic heptapeptide derived from an ACTH fragment.
Early human evidence
Neuropeptides
A synthetic tuftsin-related heptapeptide.
Early human evidence
Bioregulatory peptides
A short synthetic tripeptide studied in bioregulation models.
Preclinical foundation
Bioregulatory peptides
A tetrapeptide investigated within short-peptide bioregulation research.
Preclinical foundation
Metabolic signaling
A mitochondria-targeted tetrapeptide indexed in the literature as elamipretide and MTP-131.
Developing clinical evidence
A rehabilitation-stage comparison that followed 110 people after ischemic stroke and assessed plasma BDNF, motor performance, and Barthel index scores.
Verified PubMed record for Cortagen: Effect of tetrapeptide cortagen on regeneration of sciatic nerve.
Verified PubMed record for SS-31: Elamipretide (SS-31) improves mitochondrial dysfunction, synaptic and memory impairment induced by lipopolysaccharide in mice.
Neuroprotection
Semax has a wider publication footprint than many catalog neuropeptides, but the literature still separates mechanistic models from human inference.
Cognition
Selank’s strongest catalog value is as a mapped research cluster, not as a single simplified mechanism claim.
Neuroprotection
Cortagen’s research map is narrower than its marketing language often suggests, so the page starts with verified records and stops at their boundary.
Mitochondrial health
SS-31 has enough translational literature to deserve its own hub role, but the evidence is still endpoint- and disease-context dependent.