Evidence map›Paper›PMID 23578725›Full record

ArticleAntiviral research2013

Small molecule inhibitors of ER α-glucosidases are active against multiple hemorrhagic fever viruses.

Jinhong Chang, Travis K Warren, Xuesen Zhao, Tina Gill, Fang Guo, Lijuan Wang, Mary Ann Comunale, Yanming Du, Dominic S Alonzi, Wenquan Yu and 9 more

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

57 citing papers in PubMed, 87 citations in OpenAlex.

  1. Molecules (Basel, Switzerland) · 2026
    Review
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  8. ACS central science · 2024
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  11. Recent Advances in Therapeutic Approaches Against Ebola Virus Infection.Recent advances in anti-infective drug discovery · 2024
    Review
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  15. Article
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  17. Review
  18. Targeting Crucial Host Factors of SARS-CoV-2.ACS infectious diseases · 2020
    Review
  19. Review
  20. 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

19 authors at 5 institutions in 2 countries.

Jinhong ChangDrexel Institute for Biotechnology and Virology Research, Department of Microbiology and Immunology, Drexel University College of Medicine, Doylestown, PA 18902, United States. jinhong.chang@drexelmed.edu
Travis K Warren
Xuesen Zhao
Tina Gill
Fang Guo
Lijuan Wang
Mary Ann Comunale
Yanming Du
Dominic S Alonzi
Wenquan Yu
Hong Ye
Fei Liu
Ju-Tao Guo
Anand Mehta
Andrea Cuconati
Terry D Butters
Sina Bavari
Xiaodong Xu
Timothy M Block
Drexel University · USBaruch S. Blumberg Institute · USHepatitis B Foundation · USUnited States Army Medical Research Institute of Infectious Diseases · USUniversity of Oxford · GB

Funding

Imino sugars for flavivirus infections of bioterrorU01AI061441 · NIAID · DREXEL UNIVERSITY · PI BLOCK, TIMOTHY M · 2005 to 2010
$7.8M
Predicting HCC through GlycomicsR01CA120206 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHTA, ANAND S. · 2006 to 2016
$4.3M
Aberrantly secreted glycoproteins as markers of liver cancerU01CA168856 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHTA, ANAND S. · 2012 to 2016
$1.5M
Development of a Therapy for Dengue Virus InfectionR43AI084267 · NIAID · ENANTIGEN THERAPEUTICS, INC. · PI XU, XIAODONG · 2009 to 2009
$282k
NCI NIH HHS R01 CA120206NCI NIH HHS U01 CA168856NIAID NIH HHS AI061441NIAID NIH HHS AI084267-0109NIAID NIH HHS R43 AI084267NIAID NIH HHS U01 AI061441
6 · The paper itself

Abstract

Host cellular endoplasmic reticulum α-glucosidases I and II are essential for the maturation of viral glycosylated envelope proteins that use the calnexin mediated folding pathway. Inhibition of these glycan processing enzymes leads to the misfolding and degradation of these viral glycoproteins and subsequent reduction in virion secretion. We previously reported that, CM-10-18, an imino sugar α-glucosidase inhibitor, efficiently protected the lethality of dengue virus infection of mice. In the current study, through an extensive structure-activity relationship study, we have identified three CM-10-18 derivatives that demonstrated superior in vitro antiviral activity against representative viruses from four viral families causing hemorrhagic fever. Moreover, the three novel imino sugars significantly reduced the mortality of two of the most pathogenic hemorrhagic fever viruses, Marburg virus and Ebola virus, in mice. Our study thus proves the concept that imino sugars are promising drug candidates for the management of viral hemorrhagic fever caused by variety of viruses.

Indexed as

Glycoside Hydrolase Inhibitorsalpha-GlucosidasesAnimalsAntiviral AgentsDengueDogsDrug Evaluation, PreclinicalEbolavirusEndoplasmic ReticulumHEK293 CellsHemorrhagic Fever, EbolaHumansImino SugarsMarburgvirusMarburg Virus DiseaseMicealpha-GlucosidasesAntiviral AgentsCM-10-18 compoundglucosidase IGlycoside Hydrolase InhibitorsIHVR-11029IHVR-17028Imino Sugars

Identifiers

PMID23578725
PMCPMC3663898
OpenAlexW2019510847

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.