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Home / Peptide Library / Palmitoyl Tetrapeptide-7
Limited Research

Palmitoyl Tetrapeptide-7

Skin, Hair & Beauty · Rigin, Pal-GQPR, palmitoyl tetrapeptide-3, palmitoyl-Gly-Gln-Pro-Arg, CAS 221227-05-0

A lipidated tetrapeptide (palmitoyl-Gly-Gln-Pro-Arg) studied in dermal fibroblast and keratinocyte systems for cytokine-associated signaling, most often as one component of multi-peptide topical formulations.

🔬 Research use only — not for human or veterinary use. K4 Elite does not provide dosing instructions.
Molecular Formula
C34H62N8O7
Molecular Weight
694.92 g/mol
Research Level
Limited Research
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Palmitoyl Tetrapeptide-7 chemical structure

Palmitoyl tetrapeptide-7 is the tetrapeptide Gly-Gln-Pro-Arg conjugated to palmitic acid. It is also encountered in older literature and on some ingredient listings under its former INCI name, palmitoyl tetrapeptide-3, and under the trade name Rigin [1][2].

As with other lipidated cosmetic peptides, the palmitoyl chain is a delivery modification: it raises lipophilicity so the molecule partitions into stratum corneum lipid lamellae, a property the free tetrapeptide does not have [1].

The evidence base here is materially thinner than for the peptides it is usually formulated with. Most published human data come from multi-peptide blends, and a large share of the frequently quoted cytokine numbers originate in supplier technical documentation rather than peer-reviewed work - a limitation this entry states plainly rather than working around [1][2][3].

The proposed mechanism reported in the cosmetic-science literature is that the Gly-Gln-Pro-Arg sequence interacts with interleukin-1-beta-associated signaling and modulates NF-kB pathway activation, with reduced output of pro-inflammatory mediators including interleukin-6 in dermal fibroblast and keratinocyte systems [1][4].

This mechanism is described as proposed rather than established. The receptor-level target has not been identified in peer-reviewed work, and the peptide is characterized functionally by cytokine readouts rather than by direct target engagement [1][4].

  • Fibroblast cytokine output - studied in dermal fibroblast systems for interleukin-6 and related inflammatory mediator levels [1][4].
  • NF-kB-linked signaling - investigated as the proposed pathway for the observed cytokine modulation [4].
  • Multi-peptide topical formulations - examined in controlled studies of blends containing this peptide alongside acetyl hexapeptide-8 and palmitoyl tripeptide-1 [3].
  • Cosmetic ingredient safety - assessed in the Cosmetic Ingredient Review safety assessment of palmitoyl oligopeptides [2].
  • Skin penetration - characterized for the lipophilicity conferred by the palmitoyl chain relative to the unmodified tetrapeptide [1].
  • Peptide class reviews - contextualized within signal-peptide classification schemes for skin-directed peptides [1][5].
📋 How published studies were conducted — a research reference summarizing study designs from the literature. This is not usage, dosing, or administration guidance. K4 Elite does not provide dosing instructions; determining any research protocol is the sole responsibility of the qualified researcher.

Gorouhi and Maibach reviewed controlled ex vivo and in vivo efficacy studies of topical peptides in aged skin and grouped the field into signal peptides, enzyme-inhibitor peptides, neurotransmitter-inhibitor peptides and carrier peptides, placing palmitoyl tetrapeptide-7 among the signal peptides. The review is explicit that study quality across the class is uneven and that few peptides have been tested as isolated actives [1].

Li and colleagues evaluated a multi-peptide topical eye serum containing acetyl hexapeptide-8, palmitoyl tetrapeptide-7, palmitoyl tripeptide-1 and dipeptide-2, applied twice daily for 28 days in participants with periorbital fine lines, using instrumental and graded wrinkle measures as endpoints. Because four peptides were present, the design does not permit attribution to any single component [3].

Cell-based reports in the cosmetic-science literature describe reductions in interleukin-6 output in resting and stimulated fibroblast cultures at micromolar peptide concentrations, with DHEA used as a comparator active in some of that work. Much of this dataset derives from supplier technical documentation and has not been independently replicated in peer-reviewed publications [4].

The Cosmetic Ingredient Review panel compiled composition, use-concentration, penetration and toxicology data for palmitoyl oligopeptides as a class, including this peptide, as part of a formal safety assessment [2].

Combinations examined in the research literature. Descriptive only — not a recommendation to combine compounds.

Palmitoyl Tripeptide-1Synergistic
The most common co-formulant; the majority of published human data on either peptide come from blends containing both, which limits attribution [3].
Acetyl hexapeptide-8 (Argireline)Compatible
Different proposed mechanism; appears alongside this peptide in multi-peptide study formulations [3].
Palmitoyl pentapeptide-4 (Matrixyl)Compatible
Structurally analogous lipopeptide with a stronger controlled-study record; used as the class benchmark [1].
RetinoidsCaution
Cosmetic-science literature flags formulation pH and peptide stability as considerations when peptides are combined with retinoids.
Hyaluronic acidNeutral
Commonly co-formulated as a humectant vehicle component rather than as an interacting active [2].
  1. Gorouhi F, Maibach HI. Role of topical peptides in preventing or treating aged skin. Int J Cosmet Sci (2009)
  2. Cosmetic Ingredient Review. Safety Assessment of Palmitoyl Oligopeptides as Used in Cosmetics
  3. Li et al. Clinical evidence of the efficacy and safety of a new multi-peptide anti-aging topical eye serum. J Cosmet Dermatol (2023)
  4. Palmitoyl Tetrapeptide-7 (Rigin) ingredient monograph - Cosmetic Ingredients Guide
  5. Peptides: Emerging Candidates for the Prevention and Treatment of Skin Senescence: A Review
  6. PubChem CID 10078408 - Palmitoyl Tetrapeptide-7
What is palmitoyl tetrapeptide-7?
The tetrapeptide Gly-Gln-Pro-Arg conjugated to palmitic acid, classified in the literature as a signal peptide for skin research [1].
Is it the same as palmitoyl tetrapeptide-3?
Yes. Palmitoyl tetrapeptide-3 is the former INCI name for the same molecule; both names appear across older and newer sources [4].
What does the palmitoyl group do?
It increases lipophilicity, which penetration work associates with better partitioning into stratum corneum lipids than the unmodified tetrapeptide [1].
How strong is the evidence?
Limited. Human data come almost entirely from multi-peptide blends, and much of the cited cytokine data originates in supplier technical documentation rather than peer-reviewed studies [1][3][4].
Is this product intended for human use?
No. This material is supplied strictly for laboratory research use only. It is not a drug, food, dietary supplement, or cosmetic, and it is not intended for human or veterinary use, diagnosis, or treatment.
Disclaimer: This profile summarizes published preclinical and laboratory research for reference only. It is not medical advice and makes no claim of safety or efficacy in humans. Determining any research protocol is the sole responsibility of the qualified researcher. Products are sold strictly for in-vitro research and have not been evaluated by the FDA.