Evidence map›Paper›PMID 39105380›Full record

ReviewChemMedChem2024

Tyrosinase Inhibition and Antimelanogenic Effects of Resorcinol-Containing Compounds.

Morane Beaumet, Leticia M Lazinski, Marc Maresca, Romain Haudecoeur

Abstract readReview
In one paragraph

Review in ChemMedChem, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Moranoline-EnrichedInternational journal of molecular sciences · 2026
    Article
  5. Development of new coumarin-piperazine-N-phenylacetamid derivatives as potent tyrosinase inhibitors: In vitro and in silico evaluations.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Article
  6. Article
  7. Review
  8. Targeting Melanin Production: The Safety of Tyrosinase Inhibition.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Morane BeaumetUniv. Grenoble Alpes, CNRS, DPM, 38000, Grenoble, France.ORCID 0009-0004-2387-8876
Leticia M LazinskiUniv. Grenoble Alpes, CNRS, DPM, 38000, Grenoble, France.
Marc MarescaAix Marseille Univ., CNRS, Centrale Marseille, iSm2, 13013, Marseille, France.ORCID 0000-0002-3585-4765
Romain HaudecoeurUniv. Grenoble Alpes, CNRS, DPM, 38000, Grenoble, France.ORCID 0000-0002-6271-4717

Funding

ANRANR ("Agence Nationale de la Recherche")ARCANECBH-EUR-GS ANR-17-EURE-0003EPIDERMIS ANR-19-CE44-0002
6 · The paper itself

Abstract

Tyrosinases (TYRs) are copper-containing metalloenzymes present in a large diversity of species. In human, hTYR is responsible for pivotal steps in melanogenesis, catalysing the oxidation of l-tyrosine to l-DOPA and further to dopaquinone. While numerous TYR inhibitors have been reported, polyphenolic compounds tend to dominate the literature. However, many of these compounds, particularly monophenols and catechols, have been identified as alternative substrates rather than true inhibitors, given their structural similarity to natural substrates. Resorcinol-containing compounds have emerged as promising candidates to address this challenge, as the meta-dihydroxy moiety in resorcinol demonstrates resistance to TYR-mediated oxidation, while retaining the favourable interactions with copper ions provided by the hydroxy groups. Although their precise mechanism of action remains debated, resorcinol derivatives have yielded some of the most active compounds against isolated mushroom and human TYRs, as well as clinically used dermocosmetic agents like rucinol and thiamidol, which exhibited very promising effects in patients with facial melasma. This review outlines the development of resorcinol-containing TYR inhibitors, categorized by scaffold type, ranging from simple alkyl analogues to intricate synthetic derivatives. Mechanistic insights about the resorcinol-TYR interaction are also presented and debated.

Indexed as

Enzyme InhibitorsMelaninsMonophenol MonooxygenaseResorcinolsAnimalsHumansMolecular StructureStructure-Activity RelationshipEnzyme InhibitorsMelaninsMonophenol MonooxygenaseresorcinolResorcinolsMedicinal ChemistryMelanogenesisMelasmaMetalloenzymesTyrosinase

Identifiers

PMID39105380
PMCPMC11617669

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.