Ingredient intelligence

Azelaic acid

Pigmentation · Azelaic Acid · C9H16O4

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Azelaic acid is a nine-carbon dicarboxylic acid studied for pigmentation and . It is a regulated medicine at higher strengths in several regions.

Mechanistic only2 curated studies, none measured in people.

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Molecular identity

Two-dimensional chemical structure of Azelaic acid
Formula
C9H16O4
Molecular weight
188.22 g/mol
PubChem CID
2266
ChEBI
CHEBI:48131
Open PubChem record →

Biological targets

  • Tyrosinase (TYR)

    medium confidence

    inhibits · enzyme

    UniProt P14679
  • Kallikrein related peptidase 5 (KLK5)

    low confidence

    inhibits · enzyme

    UniProt Q9Y337

Molecules & genes

Molecules

  • Azelaic acidC9H16O4 · 188.22 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%
Azelaic acidAzelaic acidTyrosinase (TYR)TYRMelanin biosynthesisMelanogenesisStudied for post-inflamma…

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IngredientMoleculeTargetGenePathwayProcessOutcome

3 lower-confidence relationships are hidden at this filter level. Use “Show more biology” to include them.

Text alternative for this network
  • Azelaic acid is molecule Azelaic acid — high confidence
  • Azelaic acid inhibits Tyrosinase (TYR) — medium confidence
  • Tyrosinase (TYR) encoded by TYR — medium confidence
  • TYR participates in Melanin biosynthesis — medium confidence
  • Melanin biosynthesis associated with Melanogenesis — medium confidence
  • Melanogenesis studied in Studied for post-inflammatory pigmentation and redness endpoints — medium confidence

Biological pathways

Melanin biosynthesis

medium confidence

Competitive reported.

Gene Ontology GO:0042438

Evidence engine

Insufficient

Not enough curated evidence to characterise this ingredient.

Skinceptor Evidence Index

17

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

  • In-vitro1
  • Review1
Total studies
2
Human studies
0
Largest sample
Data unavailable
Range
1991–1996

Index breakdown

  • Study design quality35% × 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 volume50% × 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.

  • Recency0% × 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. 1991

    Azelaic acid: tyrosinase inhibition and selective effects on hyperactive melanocytes

    In-vitrosample size unavailable · Acta Dermato-Venereologica

  2. 1996

    Azelaic acid: tyrosinase inhibition and selective effects on hyperactive melanocytes

    Reviewsample size unavailable · Acta Dermato-Venereologica (review)

Ingredient fingerprint

10 nodes · 11 relationships · seed "azelaic-acid"

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

2 curated studies

ReviewActa Dermato-Venereologica (review) · 1996

Azelaic acid: tyrosinase inhibition and selective effects on hyperactive melanocytes

Summarises reported tyrosinase inhibition and a described preference for abnormal, hyperactive melanocytes over normal ones.

Limitations — Review, largely pre-clinical mechanism; identifier not verified during curation.

In-vitroActa Dermato-Venereologica · 1991

Azelaic acid: tyrosinase inhibition and selective effects on hyperactive melanocytes

Reported competitive tyrosinase inhibition with greater effect on hyperactive melanocytes than normal melanocytes.

Limitations — In-vitro; selectivity claim not confirmed in later human work; identifier not verified.

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