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SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesCosmeticPalmitoyl Tetrapeptide-7

Palmitoyl Tetrapeptide-7

/ Synthetic palmitoylated tetrapeptide; INCI 'Palmitoyl Tetrapeptide-7'; anti-inflammatory cosmetic peptide
SPECULATIVEN = 0 · TESTING PENDINGMW 578.70 g·mol⁻¹

ALIAS · Rigin (trade — Sederma) · Palmitoyl Tetrapeptide-7 (INCI) · Pal-GQPR

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 →

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§ A · Identity
Primary sequencePal-GQPR
MW · 578.70CLASS · Synthetic palmitoylated tetrapeptide; INCI 'Palmitoyl Tetrapeptide-7'; anti-inflammatory cosmetic peptideCATEGORY · Cosmetic

Tier 4. Sederma's Rigin (Palmitoyl Tetrapeptide-7) is marketed as an anti-inflammatory, anti-glycation cosmetic peptide. Supplier-authored ingredient dossiers cite IL-6 reduction in cytokine-stimulated fibroblast cultures. Peer-reviewed independent literature on the specific INCI is limited.

§ B · Mechanism of action

The base GQPR sequence is derived from the immunoglobulin G heavy-chain region and has been described in supplier literature as a modulator of pro-inflammatory cytokine signalling — specifically reduced IL-6 secretion in UV- or cytokine-challenged fibroblast cultures. Palmitoylation increases lipophilicity for topical delivery. The marketed claim is mitigation of low-grade chronic inflammation contributing to skin ageing.

§ C · Human clinical evidence

Tier 4. Supplier-authored cell-culture and finished-product clinical data form the primary evidence base. Peer-reviewed PubMed-indexed primary literature on Palmitoyl Tetrapeptide-7 specifically is sparse.

§ F · Safety signal

No published independent safety database. Cosmetic INCI status implies regulatory acceptance for topical use.

§ H · Regulatory status

Regulatory status

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

The IL-6 reduction mechanism, while biologically plausible, has not been independently replicated in the peer-reviewed literature in a way that is specific to topical Palmitoyl Tetrapeptide-7 in vivo on human skin.