Evidence map›Paper›PMID 41805335›Full record

ArticleJournal of medicinal chemistry2026

Design, Synthesis, and Biological Evaluation of Novel Vinyl Selenone Derivatives as Potent Nrf2 Activators for Atopic Dermatitis.

Jushin Kim, Yoowon Kim, Byungeun Kim, Elijah Hwejin Lee, Rium Kim, Jiwoo Park, Jaehwan Kim, Yonghan Kim, Sang In Park, Minsik Kang and 6 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Jushin KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Yoowon KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Byungeun KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Elijah Hwejin LeeCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Rium KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Jiwoo ParkCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Jaehwan KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Yonghan KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Sang In ParkCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Minsik KangDoping Control Center, KIST, Seoul 02792, Republic of Korea.
Jaeick LeeDoping Control Center, KIST, Seoul 02792, Republic of Korea.ORCID 0000-0001-7548-0297
Hyeon Jeong KimCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Jong-Hyun ParkCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.
Ji Won ChoiCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.ORCID 0000-0003-2990-5703
Dong-Woo LeeDepartment of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.ORCID 0000-0002-2272-8321
Ki Duk ParkCenter for Brain Disorders, Brain Science Institute, Korea Institute of Science & Technology (KIST), Seoul 02792, Republic of Korea.ORCID 0000-0002-7753-214X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atopic dermatitis (AD) is an inflammatory skin disease characterized by barrier dysfunction, immune dysregulation, and elevated oxidative stress. Since oxidative stress and inflammation are central to AD pathogenesis, activation of the Keap1-Nrf2 pathway, a regulator of antioxidant and cytoprotective defenses, has emerged as a promising therapeutic strategy for AD. We previously developed vinyl sulfone and sulfoximine compounds as potent Nrf2 activators with antioxidant and anti-inflammatory properties. In this study, we introduced a vinyl selenone core as an isosteric replacement to enhance Nrf2 activation potency. Among the synthesized compounds,

Indexed as

Anti-Inflammatory AgentsDermatitis, AtopicDrug DesignNF-E2-Related Factor 2Organoselenium CompoundsAnimalsAntioxidantsHumansKeratinocytesMiceOxidative StressRAW 264.7 CellsStructure-Activity RelationshipAnti-Inflammatory AgentsAntioxidantsNF-E2-Related Factor 2Organoselenium Compounds

Identifiers

PMID41805335
PMCPMC13071876

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.