# N-Aryl-S-aryl-2-mercaptoacetamide Derivatives Effectively Inhibit Mushroom and Cellular Tyrosinase Activities, Melanin Production, and Pigmentation in Zebrafish Larvae: Regarding Copper Ion Chelation

**Authors:** Hee Jin Jung, Hye Jin Kang, Hyeon Seo Park, Minchang Kim, Hyunju Lee, Hyunhee Ju, Yeonsoo Jeong, Yujin Park, Hae Young Chung, Hyung Ryong Moon

PMC · DOI: 10.3390/molecules31030422 · Molecules · 2026-01-26

## TL;DR

This study identifies new compounds that inhibit tyrosinase activity and melanin production more effectively than existing inhibitors in mushroom, cells, and zebrafish.

## Contribution

The discovery of N-aryl-S-aryl-2-mercaptoacetamide derivatives with superior tyrosinase inhibition and melanin suppression in multiple models.

## Key findings

- Four derivatives showed strong copper-chelating abilities but weak tyrosinase inhibition.
- Derivatives with low copper chelation exhibited potent inhibition of mushroom tyrosinase and melanin production.
- One derivative outperformed kojic acid in suppressing pigmentation in zebrafish larvae.

## Abstract

In this study, we designed and synthesized 11 N-aryl-S-aryl-2-mercaptoacetamide derivatives as new tyrosinase inhibitors (TYRIs). Experiments with pyrocatechol violet confirmed that four derivatives showed copper-chelating abilities similar to or superior to those of well-known copper-chelating TYRIs like kojic acid (KA) and N-phenylthiourea. However, these four derivatives showed little or no inhibition of mushroom TYR (mTYR) activity and melanin production in B16F10 cells. Instead, derivatives with low copper chelation ability exhibited potent inhibitory effects on mTYR activity and melanin production in B16F10 cells. These findings suggest that the results of metal ion chelation by inhibitors in an enzyme-free environment do not always match those under metalloenzyme conditions because of the interactions between inhibitors and amino acid residues around the metalloenzyme active site. Owing to their favorable interactions with amino acids in the mTYR active site, two of the derivatives inhibited mTYR more effectively than KA. Probably for the same reason, three derivatives inhibited B16F10 cellular TYR more effectively than KA, and one derivative inhibited pigment production in zebrafish larvae much better than KA. This last derivative, which effectively exhibits TYR-inhibitory activity and suppresses melanin production in several species, is considered a promising compound for use as a TYRI in various fields.

## Linked entities

- **Proteins:** LOC103429692 (polyphenol oxidase, chloroplastic-like)
- **Chemicals:** kojic acid (PubChem CID 3840), N-phenylthiourea (PubChem CID 676454), pyrocatechol violet (PubChem CID 66993)
- **Species:** Danio rerio (taxon 7955)

## Full-text entities

- **Genes:** tyr (tyrosinase) [NCBI Gene 30207] {aka sandy, zgc:109705}
- **Chemicals:** KA (MESH:C011890), metal (MESH:D008670), Melanin (MESH:D008543), pyrocatechol violet (MESH:C009134), Copper Ion (-), copper (MESH:D003300)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Agaricus bisporus (common mushroom, species) [taxon 5341]

## Full text

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## Figures

34 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12899738/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12899738/full.md

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Source: https://tomesphere.com/paper/PMC12899738