Semax

Regulatory status

Not an approved drug substance in the United States and not on the 503A bulks list. Available to verified facilities for research and manufacturing use only.

Summary

Semax is a seven-residue peptide combining an ACTH fragment with a proline-glycine-proline C-terminal extension. It is manufactured predominantly in eastern Europe, and documentation standards vary more widely than for peptides made under US or western European quality systems.

We treat the completeness of the analytical package as a qualification criterion in this line rather than a negotiating point, because incomplete certificates are the norm rather than the exception.

Typical related substances

Typical related substances are truncated ACTH fragments, oxidised methionine variants and residual acetate.

Regulatory note

Not an approved drug substance in the United States and not on the 503A bulks list.

Regulatory status shown is our current understanding and is not legal advice. Each facility is responsible for confirming eligibility for its own licence type before purchase.