Evidence map›Paper›PMID 27627626›Full record

ReviewACS infectious diseases2016

Therapeutic Potential of Spirooxindoles as Antiviral Agents.

Na Ye, Haiying Chen, Eric A Wold, Pei-Yong Shi, Jia Zhou

Abstract readReview
In one paragraph

Review in ACS infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing 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

78 citing papers in PubMed.

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18 more citing papers are in PubMed but not listed here.

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

5 authors.

Na YeChemical Biology Program, Department of Pharmacology and Toxicology, ‡Department of Biochemistry & Molecular Biology, #Sealy Center for Structural Biology & Molecular Biophysics, and ⊥Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch , 301 University Boulevard, Galveston, Texas 77555, United States.
Haiying ChenChemical Biology Program, Department of Pharmacology and Toxicology, ‡Department of Biochemistry & Molecular Biology, #Sealy Center for Structural Biology & Molecular Biophysics, and ⊥Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch , 301 University Boulevard, Galveston, Texas 77555, United States.
Eric A WoldChemical Biology Program, Department of Pharmacology and Toxicology, ‡Department of Biochemistry & Molecular Biology, #Sealy Center for Structural Biology & Molecular Biophysics, and ⊥Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch , 301 University Boulevard, Galveston, Texas 77555, United States.
Pei-Yong ShiChemical Biology Program, Department of Pharmacology and Toxicology, ‡Department of Biochemistry & Molecular Biology, #Sealy Center for Structural Biology & Molecular Biophysics, and ⊥Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch , 301 University Boulevard, Galveston, Texas 77555, United States.
Jia ZhouChemical Biology Program, Department of Pharmacology and Toxicology, ‡Department of Biochemistry & Molecular Biology, #Sealy Center for Structural Biology & Molecular Biophysics, and ⊥Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch , 301 University Boulevard, Galveston, Texas 77555, United States.

Funding

Preclinical Development of Novel Rickettsiosis Therapeutics Targeting EPAC1R01AI111464 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHENG, XIAODONG, WALKER, DAVID H · 2014 to 2018
$6.5M
5-HT2 Receptor Allosterism in Cocaine Use DisorderR01DA038446 · NIDA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Kathryn A. Cunningham, Jia Zhou · 2015 to 2026
$5.3M
Translational Explorations in Substance Use DisordersT32DA007287 · NIDA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI Kathryn A. Cunningham, Jonathan Dean Hommel · 1994 to 2026
$4.7M
Core Center for Translational Addiction SciencesP30DA028821 · NIDA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI CUNNINGHAM, KATHRYN A. · 2009 to 2010
$1.5M
NIAID NIH HHS R01 AI111464NIDA NIH HHS P30 DA028821NIDA NIH HHS R01 DA038446NIDA NIH HHS T32 DA007287
6 · The paper itself

Abstract

Antiviral therapeutics with profiles of high potency, low resistance, panserotype, and low toxicity remain challenging, and obtaining such agents continues to be an active area of therapeutic development. Due to their unique three-dimensional structural features, spirooxindoles have been identified as privileged chemotypes for antiviral drug development. Among them, spiro-pyrazolopyridone oxindoles have been recently reported as potent inhibitors of dengue virus NS4B, leading to the discovery of an orally bioavailable preclinical candidate (R)-44 with excellent in vivo efficacy in a dengue viremia mouse model. This review highlights recent advances in the development of biologically active spirooxindoles for their antiviral potential, primarily focusing on the structure-activity relationships (SARs) and modes of action, as well as future directions to achieve more potent analogues toward a viable antiviral therapy.

Indexed as

AnimalsAntiviral AgentsDrug DiscoveryHumansIndolesMiceOxindolesStructure-Activity RelationshipVirus DiseasesViruses2-oxindoleAntiviral AgentsIndolesOxindolesantiviral agentsDENVHIVinfluenza virusRSVspirooxindoles

Identifiers

PMID27627626
PMCPMC5417367

What OpenQuestion holds

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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.