Evidence map›Paper›PMID 41159291›Full record

ArticleJournal of cosmetic dermatology2025

KT-939: A Next-Generation Human Tyrosinase Inhibitor With Superior Efficacy for the Safe Management of Hyperpigmentation.

Xiaodan Hou, Yunhui Li, Qun Zhang, Honghua Yan, Xin Zhang, Yueying Yang, Xiang Cai, Jin Wang, Miaohua Ding, Dong Chen and 4 more

Abstract read
In one paragraph

Article in Journal of cosmetic dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Xiaodan HouKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Yunhui LiKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Qun ZhangKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Honghua YanKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Xin ZhangKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Yueying YangKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Xiang CaiKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Jin WangKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Miaohua DingKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Dong ChenKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Jie ChenKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Youzhi TongKintor Pharmaceutical Limited, Suzhou, Jiangsu, China.
Nina MehtaThe University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.ORCID https://orcid.org/0000-0001-7745-9993
Andy GorenUniversity of Rome "G. Marconi", Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTyrosinase is the rate-limiting enzyme in melanin biosynthesis, and its overactivity contributes to hyperpigmentation disorders. Existing tyrosinase inhibitors are often limited by poor potency against human tyrosinase (hTYR) or safety concerns.

aimsTo evaluate the inhibitory potency, safety, and multifunctional activity of KT-939, a newly synthesized human tyrosinase inhibitor, compared with established depigmenting agents. PATIENTS/

methodsKT-939 was synthesized and tested in vitro for tyrosinase inhibition, melanin suppression in human melanocytes, antioxidant activity (DPPH radical scavenging, NRF2 pathway activation), and anti-inflammatory activity (cytokine expression in LPS-stimulated macrophages). Safety was assessed in multiple skin-related cell lines. A 28-day, single-center clinical study in healthy women with sensitive skin assessed the effects of 0.2% KT-939 lotion on pigmentation and tolerability.

resultsKT-939 strongly inhibited hTYR (IC₅₀ = 0.07 μM), demonstrating ~4-fold greater potency than Thiamidol and far surpassing other comparators. In melanocytes, KT-939 reduced melanin production (IC₅₀ = 0.36 μM) with reversible effects upon withdrawal. KT-939 also displayed antioxidant activity, NRF2 activation, and suppression of pro-inflammatory cytokines, without cytotoxicity up to 50 μM. Clinically, 28 days of KT-939 lotion use improved skin spot lightening, tone uniformity, and overall brightness, with good tolerability in sensitive skin.

conclusionsKT-939 is a potent and safe human tyrosinase inhibitor with additional antioxidant and anti-inflammatory activity. These findings support its potential in cosmetic skin brightening and as a therapeutic candidate for hyperpigmentation disorders.

Indexed as

Enzyme InhibitorsHyperpigmentationMonophenol MonooxygenaseSkin Lightening PreparationsAdultAntioxidantsCell LineFemaleHumansMelaninsMelanocytesMiddle AgedNF-E2-Related Factor 2Skin PigmentationAntioxidantsEnzyme InhibitorsMelaninsMonophenol MonooxygenaseNFE2L2 protein, humanNF-E2-Related Factor 2Skin Lightening PreparationshyperpigmentationKT‐939melanogenesistyrosinase

Identifiers

PMID41159291
PMCPMC12569736

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Registered trials

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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.