Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Antimicrobial / Immune
Also known as: Cathelicidin fragment
An antimicrobial peptide studied for immune and antimicrobial roles. Mostly preclinical.
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LL-37 is a human cathelicidin-derived antimicrobial peptide.
Limited; largely mechanistic and preclinical.
Human safety data is limited; research-market material is unverified.
Not an approved medicine. Research chemical status.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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LL-37 is a human cathelicidin-derived antimicrobial peptide.
LL-37 is the only known human cathelicidin-derived antimicrobial peptide, a 37-amino-acid fragment released from the precursor protein hCAP18. As a naturally occurring component of the innate immune system, it is found in neutrophils, epithelial surfaces, sweat, and skin, where it forms part of the body's first line of host defense. On peptides.cx it is catalogued in the Antimicrobial / Immune category, and it is important to be clear at the outset: LL-37 is not an approved medicine. Material sold on the research-chemical market carries research-chemical status, is unverified, and is not intended for human use.
LL-37 is studied because it sits at the intersection of two functions that interest researchers: direct antimicrobial activity and broader immune modulation. In laboratory and preclinical work it has been reported to disrupt bacterial membranes and to influence immune signaling, wound-related processes, and inflammatory pathways, which is why much of the discussion around it centers on immune support and skin biology. However, the honest evidence picture is modest. The bulk of what is known comes from in-vitro (cell and test-tube) experiments and animal models; direct human clinical evidence remains limited and largely mechanistic. peptides.cx assigns LL-37 an evidence grade of C, reflecting that its roles are biologically well-characterized in principle but not established through controlled human outcome trials.
Because LL-37 is an endogenous immune peptide, its biology is genuinely complex β the same molecule that shows antimicrobial and immune-modulating activity has also been linked in research contexts to inflammatory and autoimmune processes, underscoring that "natural" does not mean simple or automatically beneficial. Long-term human safety data is limited, and the profile of unregulated research-market material is unknown. This page summarizes what LL-37 is, why it is researched, and where the evidence currently stands, so readers can understand the science accurately rather than the marketing. It is educational reference information only and is not medical advice.
Evidence grade: C
Limited; largely mechanistic and preclinical. Antimicrobial and immune effects reported.
Limited; largely mechanistic and preclinical.
Antimicrobial and immune effects reported.
Human safety data is limited; research-market material is unverified.
Not an approved medicine. Research chemical status.
1980s
Cathelicidins are identified as a family of host-defense (antimicrobial) peptides in mammals, setting the stage for finding a human member.
mid-1990s
The sole human cathelicidin (hCAP18) is characterized and its released C-terminal peptide is named LL-37, after its two leading leucine residues and length of 37 amino acids.
late 1990s
Early preclinical work describes LL-37's broad antimicrobial activity against bacteria and its presence in neutrophils, skin, and other tissues.
2000s
Research broadens beyond killing microbes to immune-modulating roles, and LL-37 is implicated in skin conditions and wound-healing biology in laboratory and animal studies.
2010s
Preclinical interest expands to areas such as antimicrobial resistance and possible anticancer signaling, while human clinical evidence remains sparse.
early 2020s
LL-37 continues to be studied largely at the mechanistic and preclinical level; it is not an approved medicine and circulates in research-chemical channels with unverified material quality.