Skip to main content
SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesCosmetic, LongevityHexapeptide-44

Hexapeptide-44

/ Synthetic hexapeptide; INCI 'Hexapeptide-44'; lamin B1 upregulating cosmetic peptide
SPECULATIVEN = 0 · TESTING PENDING

ALIAS · Hexalin (trade) · Hexapeptide-44 (INCI)

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

Terms in this page you can click for a plain-English popup: , , , , , , , .

§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Synthetic hexapeptide; INCI 'Hexapeptide-44'; lamin B1 upregulating cosmetic peptideCATEGORY · Cosmetic, Longevity

Tier 4. Industry-authored cosmetic ingredient. The supplier marketing literature describes lamin B1 upregulation in skin fibroblast cultures as the proposed anti-senescence mechanism. PubMed-indexed primary literature on Hexapeptide-44 specifically is sparse to absent; the molecule is documented mainly in supplier dossiers and INCI/cosmetic-trade publications.

§ B · Mechanism of action

Hexapeptide-44 is described in supplier technical literature as an upregulator of lamin B1 — a nuclear-envelope intermediate filament protein whose decline is associated with replicative senescence in dermal fibroblasts. The proposed mechanism is restoration of nuclear-envelope integrity in aged fibroblasts, with downstream effects on chromatin organisation and gene-expression patterns characteristic of younger cells. Independent peer-reviewed mechanism characterisation is limited.

§ C · Human clinical evidence

Tier 4. Supplier-authored in-vitro fibroblast studies and trade-publication summaries are the primary evidence sources. PubMed-indexed independent replication and controlled human topical-efficacy trials are not readily available.

§ F · Safety signal

No published independent safety database. Cosmetic INCI status implies acceptance for topical use in finished products under standard cosmetic-ingredient regulatory frameworks; this is not the same as a clinical safety dataset.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

The lamin B1 mechanism is biologically plausible (lamin B1 loss is a documented senescence marker) but the published evidence that topical Hexapeptide-44 modulates lamin B1 in human skin in vivo is industry-authored. Independent peer-reviewed replication of the mechanism and clinical-grade efficacy data are limited.