Evidence map›Paper›PMID 31964798›Full record

ArticleAntimicrobial agents and chemotherapy2020

6'-β-Fluoro-Homoaristeromycin and 6'-Fluoro-Homoneplanocin A Are Potent Inhibitors of Chikungunya Virus Replication through Their Direct Effect on Viral Nonstructural Protein 1.

Kristina Kovacikova, Bas M Morren, Ali Tas, Irina C Albulescu, Robin van Rijswijk, Dnyandev B Jarhad, Young Sup Shin, Min Hwan Jang, Gyudong Kim, Hyuk Woo Lee and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  10. ACS central science · 2024
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  19. Current Status of Chikungunya in India.Frontiers in microbiology · 2021
    Review
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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

13 authors at 2 institutions in 2 countries.

Kristina KovacikovaDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.
Bas M MorrenDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.
Ali TasDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.
Irina C AlbulescuDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.
Robin van RijswijkDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.
Dnyandev B JarhadCollege of Pharmacy, Seoul National University, Seoul, South Korea.
Young Sup ShinCollege of Pharmacy, Seoul National University, Seoul, South Korea.
Min Hwan JangCollege of Pharmacy, Seoul National University, Seoul, South Korea.
Gyudong KimCollege of Pharmacy, Seoul National University, Seoul, South Korea.
Hyuk Woo LeeFuture Medicine Co., Ltd., Seoul, South Korea.
Lak Shin JeongCollege of Pharmacy, Seoul National University, Seoul, South Korea.
Eric J SnijderDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0003-3297-2309
Martijn J van HemertDepartment of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands M.J.van_Hemert@lumc.nl.ORCID 0000-0002-2617-9243
Leiden University Medical Center · NLSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alphaviruses are arthropod-borne, positive-stranded RNA viruses capable of causing severe disease with high morbidity. Chikungunya virus (CHIKV) is an alphavirus that causes a febrile illness which can progress into chronic arthralgia. The current lack of vaccines and specific treatment for CHIKV infection underscores the need to develop new therapeutic interventions. To discover new antiviral agents, we performed a compound screen in cell culture-based infection models and identified two carbocyclic adenosine analogues, 6'-β-fluoro-homoaristeromycin (FHA) and 6'-fluoro-homoneplanocin A (FHNA), that displayed potent activity against CHIKV and Semliki Forest virus (SFV) with 50% effective concentrations in the nanomolar range at nontoxic concentrations. The compounds, designed as inhibitors of the host enzyme

Indexed as

AdenosineAnimalsAntiviral AgentsChikungunya virusChlorocebus aethiopsDose-Response Relationship, DrugDrug Evaluation, PreclinicalDrug Resistance, ViralGuanosine MonophosphateMutationPhosphorus RadioisotopesSemliki forest virusVero CellsViral Nonstructural ProteinsVirus Replication6'-beta-fluoro-homoaristeromycinAdenosineAntiviral Agentsfluoro-homoneplanocin AGuanosine MonophosphatePhosphorus-32Phosphorus RadioisotopesViral Nonstructural Proteins6′-fluoro-homoneplanocin A6′-β-fluoro-homoaristeromycinalphavirusantiviral agentscappingchikungunya virusnsP1SAH hydrolase

Identifiers

PMID31964798
PMCPMC7179274
OpenAlexW3001098727

What OpenQuestion 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 OpenQuestion graph.