Evidence map›Paper›PMID 32866370›Full record

ArticleACS infectious diseases2020

JMX0207, a Niclosamide Derivative with Improved Pharmacokinetics, Suppresses Zika Virus Infection Both

Zhong Li, Jimin Xu, Yuekun Lang, Xiaoyu Fan, Lili Kuo, Lianna D'Brant, Saiyang Hu, Subodh Kumar Samrat, Nicole Trudeau, Anil M Tharappel and 9 more

Open access · greenAbstract read
In one paragraph

Article in ACS infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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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

19 authors at 4 institutions in 1 country.

Zhong LiWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Jimin XuChemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, Texas 77555, United States.
Yuekun LangWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Xiaoyu FanDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona 85721, United States.
Lili KuoWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Lianna D'BrantThe Neural Stem Cell Institute, 1 Discovery Drive, Rensselaer, New York 12144, United States.
Saiyang HuWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Subodh Kumar SamratWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Nicole TrudeauThe Neural Stem Cell Institute, 1 Discovery Drive, Rensselaer, New York 12144, United States.
Anil M TharappelWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Natasha RugensteinThe Neural Stem Cell Institute, 1 Discovery Drive, Rensselaer, New York 12144, United States.
Cheri A KoetznerWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Jing ZhangWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
Haiying ChenChemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, Texas 77555, United States.
Laura D KramerWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.
David ButlerThe Neural Stem Cell Institute, 1 Discovery Drive, Rensselaer, New York 12144, United States.
Qing-Yu ZhangDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona 85721, United States.
Jia ZhouChemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, Texas 77555, United States.ORCID 0000-0002-2811-1090
Hongmin LiWadsworth Center, New York State Department of Health, 120 New Scotland Avenue, Albany, New York 12208, United States.ORCID 0000-0002-8684-5308
New York State Department of Health · USNeural Stem Cell Institute · USThe University of Texas Medical Branch at Galveston · USUniversity of Arizona · US

Funding

High throughput screening of orthosteric inhibitors of flavivirus proteaseR01AI131669 · NIAID · WADSWORTH CENTER · PI LI, HONGMIN · 2018 to 2022
$2.6M
High throughput screening of orthosteric inhibitors of flavivirus proteaseR56AI131669 · NIAID · WADSWORTH CENTER · PI LI, HONGMIN · 2017 to 2017
$524k
Identification and characterization of allosteric inhibitors of Zika protease by targeting the NS2B conformational changeR21AI140491 · NIAID · WADSWORTH CENTER · PI LEMASTER, DAVID M, LI, HONGMIN · 2018 to 2019
$460k
In vivo efficacy studies of existing drugs re-purposed for flaviviruses in mouse modelsR21AI133219 · NIAID · WADSWORTH CENTER · PI LI, HONGMIN · 2017 to 2018
$452k
New Use of Old Drugs for Zika VirusR21AI134568 · NIAID · WADSWORTH CENTER · PI LI, HONGMIN · 2017 to 2018
$447k
NIAID NIH HHS R01 AI131669NIAID NIH HHS R21 AI133219NIAID NIH HHS R21 AI134568NIAID NIH HHS R21 AI140491NIAID NIH HHS R56 AI131669
6 · The paper itself

Abstract

Flaviviruses causes significant human disease. Recent outbreaks of the Zika virus highlight the need to develop effective therapies for this class of viruses. Previously we identified niclosamide as a broad-spectrum inhibitor for flaviviruses by targeting the interface between viral protease NS3 and its cofactor NS2B. Here, we screened a small library of niclosamide derivatives and identified a new analogue with improved pharmacokinetic properties. Compound JMX0207 showed improved efficacy in inhibition of the molecular interaction between NS3 and NS2B, better inhibition of viral protease function, and enhanced antiviral efficacy in the cell-based antiviral assay. The derivative also significantly reduced Zika virus infection on 3D mini-brain organoids derived from pluripotent neural stem cells. Intriguingly, the compound significantly reduced viremia in a Zika virus (ZIKV) animal model. In summary, a niclosamide derivative, JMX0207, was identified, which shows improved pharmacokinetics and efficacy against Zika virus both

Indexed as

FlavivirusZika VirusZika Virus InfectionAnimalsHumansNiclosamideViral Nonstructural ProteinsNiclosamideViral Nonstructural ProteinsantiviralDengue virusFlavivirusprotease inhibitorZika virus

Identifiers

PMID32866370
PMCPMC7559020
OpenAlexW3082172843

What OpenQuestion holds

Textmetadata
LicenceTDM
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.