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Reference information only. Therapept does not sell peptides and does not provide medical advice.Research-use notice

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37-residue peptide derived from human cathelicidin

Cathelicidin LL-37

A 37-residue peptide derived from the human cathelicidin protein. No FDA-approved drug product exists, and FDA lists it among bulk substances whose compounding nominations were withdrawn.

UnapprovedAlso listed as: LL-37, CAP18, Ropocamptide

Why people are interested in Cathelicidin LL-37

A 37-residue peptide derived from the human cathelicidin protein. No FDA-approved drug product exists, and FDA lists it among bulk substances whose compounding nominations were withdrawn.

  • Antimicrobial peptides— a research-category classification, not a claimed use
  • Preclinical research compounds— a research-category classification, not a claimed use

Where the interest comes from differs by compound: published research, an approved use, clinical discussion, community discussion and vendor claims are different things. This page keeps them apart — the sections below say which kind of source supports each statement.

Quick facts

Molecular weight
4493 g/mol
Sequence length
37 chars
CAS number
154947-66-7
PubChem CID
16198951

0 evidence records indexed · 0 clinical trials · last reviewed 15 September 2026

Research at a glance

No evidence records in this file yet.

Open the full evidence file

What has actually been studied

    What is still unknown

    What we know

      Editorial reading of the records below, labelled as Therapept analysis. How records are built

      What remains uncertain

        Preparation and handling

        Lyophilized peptides ship as powders; whatever happens next involves diluents, concentrations and storage conditions that are compound- and product-specific. Therapept’s preparation guides explain the vocabulary and the arithmetic; the product’s own documentation states its requirements.

        United States regulatory status

        No FDA-approved product

        • No approved drug product exists in Drugs@FDA.
        • Listed as “Cathelicidin LL-37” on FDA's table of bulk substances nominated for compounding and withdrawn. FDA's published concerns include immunogenicity risk for certain routes, peptide-related impurities and API characterisation, and insufficient safety information.
        • FDA's entry also notes nonclinical findings suggesting detrimental effects on male reproduction and that the substance can be protumorigenic in some tissues.
        • Not named on the WADA 2026 Prohibited List.

        Regulatory status describes how a substance is classified. It is not a safety assessment, and it says nothing about the quality of any particular material.

        Technical identity

        Compound class
        37-residue peptide derived from human cathelicidin; antimicrobial peptide
        Sequence
        LLGDFFRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES
        Molecular formula
        C205H340N60O53
        Molecular weight
        4493 g/mol
        CAS number
        154947-66-7
        PubChem CID
        16198951
        Research categories
        Antimicrobial peptides, Preclinical research compounds