Evidence map›Paper›PMID 41891956›Full record

ArticleInternational journal of molecular medicine2026

Novel Hsp90 inhibitor JD‑02 inhibits HSV‑1 infection via the Raf/MEK/ERK signaling pathway.

Yexuan Zhu, Xiaohui Wang, Jiaying Lin, Xiao Wang, Kai Zheng, Zhe Ren, Ji Xiao, Yifei Wang

Abstract read
In one paragraph

Article in International journal of molecular medicine, 2026. 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

8 authors.

Yexuan Zhu *Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Xiaohui Wang *Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Jiaying Lin *Guangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Xiao WangDepartment of Pharmacy, Shenzhen People's Hospital, The Second Clinical Medical College, Shenzhen, Guangdong 518020, P.R. China.
Kai ZhengSchool of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen, Guangdong 518060, P.R. China.
Zhe RenGuangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Ji XiaoGuangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.
Yifei WangGuangzhou Jinan Biomedicine Research and Development Center, National Engineering Research Center of Genetic Medicine, Institute of Biomedicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herpes simplex virus type 1 (HSV‑1) is a neurotropic pathogen with an extremely high infection rate. The excessive use of acyclovir (ACV) and nucleoside analogs has resulted in the emergence of drug‑resistant HSV‑1 strains, thereby underscoring the need for the development of novel therapeutic agents against HSV‑1. The present study sought to evaluate the efficacy and elucidate the mechanism of action of the novel Hsp90 inhibitor, JD‑02, in the context of HSV‑1 infection, as well as to assess its potential as an anti‑HSV‑1 therapeutic agent. The results of the present study demonstrated that JD‑02 exhibits lower cytotoxicity relative to the conventional Hsp90 inhibitor, AT533, and effectively inhibits infection by both standard and ACV‑resistant HSV‑1 strains

Indexed as

Antiviral AgentsHerpes SimplexHerpesvirus 1, HumanHSP90 Heat-Shock ProteinsMAP Kinase Signaling Systemraf KinasesAnimalsChlorocebus aethiopsFemaleHumansMiceVero CellsAntiviral AgentsHSP90 Heat-Shock Proteinsraf KinasesantiviralHSV‑1JD‑02Raf/MEK/ERK signal pathwayUL30

Identifiers

PMID41891956
PMCPMC13042271

What OpenQuestion holds

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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.