Molecular profile
- Class
- Cationic human host-defense peptide
- Sequence
- LLGDFFRKSKEKIGKEFKRIVQRIKDFLRNLVPRTES
- Amino acids
- 37
- Approx. MW
- 4493.3 Da
- Origin / design
- Proteolytic product of the hCAP18 cathelicidin precursor
Peptide research profile
Also known as hCAP18-derived cathelicidin · CAP-18
The 37-residue human cathelicidin host-defense peptide. It has broad antimicrobial and immunomodulatory biology plus topical wound trials, but systemic use remains unestablished.
Dosing literacy
The 100 mcg twice-daily calculator row is not the regimen used in human wound trials, which applied topical LL-37 at defined concentrations. This is educational source context—not a protocol or recommendation.
Scaling framework
There is no regulator-approved starting dose for this research use. A low-looking number is not automatically safe.
This is the range represented in the in-app protocol library. It describes the source record; it does not validate the regimen.
Higher exposure is not established as more effective. Human pharmacokinetic and long-term safety data may be absent.
Concentration applied to a wound (mg/mL) is not convertible to an injected whole-body dose using the calculator.
Schedule literacy
The cadence represented by the recorded calculator presets.
Published experiments may use a different route, formulation, timing, or population and should not be treated as interchangeable.
No single schedule has been validated across products or research contexts.
Human evidence is route-specific: 0.5 and 1.6 mg/mL topical solutions showed early signals, while later results were mixed.
Research best practices
Keep cold, dry, and protected from light according to the manufacturer certificate or validated lab SOP.
Use sterile technique, refrigerate as validated, and avoid repeated freeze–thaw cycles.
Record lot, concentration, preparation date, and the identity/purity documentation used by the lab.
Research orientation
These themes describe recurring questions in published research. They are not claims of effectiveness or recommendations for use.
Laboratory studies cover bacteria, fungi, viruses, biofilms, and membrane interactions.
LL-37 can act in pro- or anti-inflammatory directions depending on context.
Topical trials evaluate hard-to-heal venous and diabetic ulcers.
Expression and signaling can be context-dependent and potentially bidirectional.
Evidence map
Study models remain visible so laboratory and animal findings are not mistaken for established human outcomes.
A small phase I/II trial showed dose-dependent healing signals; a larger phase IIb study was negative overall.
Clinical evidence concerns local topical concentrations, not systemic injection.
Reviews emphasize antimicrobial, chemotactic, angiogenic, and inflammatory effects that vary by environment.
Recorded protocol library
These amount records are independent from vial strength, reconstitution volume and measuring device. A recorded source is not the same as study backing, and these values are not recommendations.
100 mcg
Sign in for schedule, duration and source context.
500 mcg
Sign in for schedule, duration and source context.
Technical reference
Curated sources