Evidence map›Paper›PMID 35862746›Full record

ArticleAntimicrobial agents and chemotherapy2022

Hinokiflavone Attenuates the Virulence of Methicillin-Resistant Staphylococcus aureus by Targeting Caseinolytic Protease P.

Xiangri Kong, Bingmei Wang, Xiaoyu Chen, Li Wang, Xingye Wang, Juan Hou, Lin Wei, Liyan Sui, Chi Zhang, Jiyu Guan and 4 more

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2022. 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
1.2field-weighted citation impact, top 22% of its field
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, 15 citations in OpenAlex.

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  6. Investigating the effect ofIn silico pharmacology · 2024
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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 at 3 institutions in 1 country.

Xiangri KongChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Bingmei WangChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Xiaoyu ChenChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Li WangChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Xingye WangChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Juan HouChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Lin WeiChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Liyan SuiCenter for Pathogen Biology and Infectious Diseases, Key Laboratory of Organ Regeneration and Transplantation of the Ministry of Education, The First Hospital Jilin University, Changchun, People's Republic of China.
Chi ZhangChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Jiyu GuanKey Laboratory of Zoonosis, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun, People's Republic of China.
Yanhe LuanAffiliated Hospital to Changchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Wei WangChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.
Wu SongChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.ORCID 0000-0002-1314-8018
Yicheng ZhaoChangchun University of Chinese Medicinegrid.440665.5, Changchun, People's Republic of China.ORCID 0000-0002-1691-323X
Changchun University of Chinese Medicine · CNJilin University · CNThe Affiliated Hospital to Changchun University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug-resistant bacteria was the third leading cause of death worldwide in 2019, which sounds like a cautionary note for global public health. Therefore, developing novel strategies to combat Methicillin-resistant Staphylococcus aureus (MRSA) infections is the need of the hour. Caseinolytic protease P (ClpP) represents pivotal microbial degradation machinery in MRSA involved in bacterial homeostasis and pathogenicity, considered an ideal target for combating S. aureus infections. Herein, we identified a natural compound, hinokiflavone, that inhibited the activity of ClpP of MRSA strain USA300 with an IC

Indexed as

Methicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsAnimalsAnti-Bacterial AgentsBiflavonoidsMiceMolecular Docking SimulationPeptide HydrolasesStaphylococcus aureusVancomycinVirulenceAnti-Bacterial AgentsBiflavonoidshinokiflavonePeptide HydrolasesVancomycinCaseinolytic protease Phinokiflavoneinfectionmethicillin-resistant Staphylococcus aureuspneumonia

Identifiers

PMID35862746
PMCPMC9380526
OpenAlexW4285043404

What OpenQuestion holds

Textmetadata
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.