Evidence map›Paper›PMID 39085352›Full record

ArticleExperimental & molecular medicine2024

A dual inhibitor of PIP5K1C and PIKfyve prevents SARS-CoV-2 entry into cells.

Yuri Seo, Yejin Jang, Seon-Gyeong Lee, Joon Ho Rhlee, Sukyeong Kong, Thi Tuyet Hanh Vo, Myung Hun Kim, Myoung Kyu Lee, Byungil Kim, Sung You Hong and 3 more

Abstract read
In one paragraph

Article in Experimental & molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Review
  3. How endosomal PIKfyve inhibition prevents viral membrane fusion and entry.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Targeting IPNature communications · 2026
    Article
  6. Article
  7. PIKfyve mediates the maturation of mycobacteria-containing vesicles.Frontiers in cellular and infection microbiology · 2026
    Article
  8. Article
  9. 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

13 authors.

Yuri Seo *Graduate School of Analytical Science and Technology, Chungnam National University, Daejeon, Republic of Korea.
Yejin Jang *Infectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, Republic of Korea.
Seon-Gyeong Lee *Center for Genomic Integrity, Institute for Basic Science (IBS), Ulsan, Republic of Korea.
Joon Ho RhleeDepartment of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
Sukyeong KongCenter for Genomic Integrity, Institute for Basic Science (IBS), Ulsan, Republic of Korea.
Thi Tuyet Hanh VoGraduate School of Analytical Science and Technology, Chungnam National University, Daejeon, Republic of Korea.
Myung Hun KimGraduate School of Analytical Science and Technology, Chungnam National University, Daejeon, Republic of Korea.
Myoung Kyu LeeInfectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, Republic of Korea.
Byungil KimInfectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-1743-2657
Sung You HongCenter for Genomic Integrity, Institute for Basic Science (IBS), Ulsan, Republic of Korea.
Meehyein KimInfectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, Republic of Korea. mkim@krict.re.kr.
Joo-Yong LeeGraduate School of Analytical Science and Technology, Chungnam National University, Daejeon, Republic of Korea. leejooyong@cnu.ac.kr.ORCID http://orcid.org/0000-0003-1049-6006
Kyungjae MyungCenter for Genomic Integrity, Institute for Basic Science (IBS), Ulsan, Republic of Korea. kmyung@ibs.re.kr.ORCID http://orcid.org/0000-0001-7975-6190

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 pandemic has had an unprecedented impact on global public health and the economy. Although vaccines and antivirals have provided effective protection and treatment, the development of new small molecule-based antiviral candidates is imperative to improve clinical outcomes against SARS-CoV-2. In this study, we identified UNI418, a dual PIKfyve and PIP5K1C inhibitor, as a new chemical agent that inhibits SARS-CoV-2 entry into host cells. UNI418 inhibited the proteolytic activation of cathepsins, which is regulated by PIKfyve, resulting in the inhibition of cathepsin L-dependent proteolytic cleavage of the SARS-CoV-2 spike protein into its mature form, a critical step for viral endosomal escape. We also demonstrated that UNI418 prevented ACE2-mediated endocytosis of the virus via PIP5K1C inhibition. Our results identified PIKfyve and PIP5K1C as potential antiviral targets and UNI418 as a putative therapeutic compound against SARS-CoV-2.

Indexed as

Antiviral AgentsCOVID-19Phosphatidylinositol 3-KinasesPhosphotransferases (Alcohol Group Acceptor)SARS-CoV-2Spike Glycoprotein, CoronavirusVirus InternalizationAngiotensin-Converting Enzyme 2AnimalsCathepsin LChlorocebus aethiopsCOVID-19 Drug TreatmentEndocytosisHEK293 CellsHumansVero Cells1-phosphatidylinositol-4-phosphate 5-kinaseACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsCathepsin LCTSL protein, humanPhosphatidylinositol 3-KinasesPhosphotransferases (Alcohol Group Acceptor)PIKFYVE protein, humanSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID39085352
PMCPMC11372076

What OpenQuestion holds

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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 OpenQuestion graph.