Ingredient intelligence

Retinaldehyde

Retinoid · Retinal · C20H28O

Retinaldehyde sits one oxidation step closer to retinoic acid than retinol, and is studied as a cosmetic retinoid with the same receptor-mediated mechanism downstream.

Molecular identity

Two-dimensional chemical structure of Retinaldehyde
Formula
C20H28O
Molecular weight
284.4 g/mol
PubChem CID
638015
ChEBI
CHEBI:17898
Open PubChem record →

Biological targets

  • Retinaldehyde dehydrogenase (ALDH1A1)

    high confidence

    targets · enzyme

    UniProt P00352
  • Retinoic acid receptor gamma (RARG)

    medium confidence

    activates · receptor

    Indirect, via oxidation to retinoic acid.

    UniProt P13631

Molecules & genes

Molecules

  • RetinaldehydeC20H28O · 284.4 g/mol

Genes / proteins

How could this ingredient interact with biology?

Biological network

Ingredient → molecule → target → gene/protein → pathway → process → studied outcome. Relationship strength is drawn from the curated confidence tier; nothing is added to make the chain look complete.

100%
RetinaldehydeRetinaldehydeRetinaldehyde dehydrogena…Retinoic acid receptor ga…ALDH1A1RARGRetinoid metabolism and t…Epidermal cell turnover

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IngredientMoleculeTargetGenePathwayProcessOutcome

1 lower-confidence relationship is hidden at this filter level. Use “Show more biology” to include them.

Text alternative for this network
  • Retinaldehyde is molecule Retinaldehydehigh confidence
  • Retinaldehyde targets Retinaldehyde dehydrogenase (ALDH1A1)high confidence
  • Retinaldehyde activates Retinoic acid receptor gamma (RARG)medium confidence
  • Retinaldehyde dehydrogenase (ALDH1A1) encoded by ALDH1A1high confidence
  • Retinoic acid receptor gamma (RARG) encoded by RARGmedium confidence
  • ALDH1A1 participates in Retinoid metabolism and transporthigh confidence
  • RARG participates in Retinoid metabolism and transportmedium confidence
  • Retinoid metabolism and transport associated with Epidermal cell turnovermedium confidence

Biological pathways

Retinoid metabolism and transport

high confidence

Oxidation of retinaldehyde to retinoic acid.

Reactome R-HSA-975634

Evidence engine

Insufficient

Not enough curated evidence to characterise this ingredient.

Skinceptor Evidence Index

20

experimental · of 100

This index is a research-navigation aid describing how much evidence exists and how it was produced. It is not a medical safety score, an efficacy guarantee, or a clinical recommendation.

Study composition

  • Review1
Total studies
1
Human studies
0
Largest sample
Data unavailable
Range
2015–2015

Index breakdown

  • Study design quality45% × 28%

    Mean design weight across curated studies (meta-analysis 1.0, RCT 0.9, other human 0.7, review 0.45, animal 0.35, in-vitro 0.25).

  • Human evidence share0% × 22%

    Proportion of curated evidence measured in people rather than cells or animals.

  • Evidence volume32% × 14%

    Log-scaled count of curated studies, so volume alone cannot dominate the score.

  • Largest sample size0% × 12%

    Log-scaled largest reported sample size across curated human studies.

  • Replication0% × 12%

    Independent human studies, capped at three; one study is never treated as replicated.

  • Recency45% × 7%

    Linear decay over a twenty-year window from the most recent curated publication.

  • Source traceability0% × 5%

    Share of curated studies with a verified PMID or DOI in this dataset.

How is this determined? →

Insufficient comparable evidence for quantitative synthesis.

Research timeline

How the evidence accumulated

  1. 2015

    Retinoic acid receptor expression and retinoid signalling in human skin

    Reviewsample size unavailable · Journal of Investigative Dermatology (review)

Ingredient fingerprint

9 nodes · 9 relationships · seed "retinaldehyde"

The fingerprint is a deterministic visual signature: ridge amplitude comes from the number of entities in each tier, node placement from identifier hashes, and opacity from confidence. Two ingredients can never produce the same figure unless their networks are identical.

Open in Biology as Art →

Research

1 curated study

ReviewJournal of Investigative Dermatology (review) · 2015

Retinoic acid receptor expression and retinoid signalling in human skin

Summarises RAR/RXR heterodimer signalling as the transcriptional mechanism of retinoid action in epidermis and dermis.

LimitationsNarrative review; mechanistic focus without effect-size synthesis.

Identifier not curated — search Europe PMCRetinol · All-trans retinoic acid · Retinaldehyde

Community evidence

Submitted by readers

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Reader submissions appear here only after review. They are not part of the curated dataset and do not affect the Skinceptor Evidence Index.

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Sources