Evidence map›Paper›PMID 31671622›Full record

ReviewDiseases (Basel, Switzerland)2019

HIV Capsid Inhibitors Beyond PF74.

Carole McArthur, Fabio Gallazzi, Thomas P Quinn, Kamal Singh

Abstract readReview
In one paragraph

Review in Diseases (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Antiviral Properties of HIV-1 Capsid Inhibitor GSK878.Antimicrobial agents and chemotherapy · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. An Update on Antiretroviral Therapy.Advances in experimental medicine and biology · 2021
    Article
  13. Viral structural proteins as targets for antivirals.Current opinion in virology · 2020
    Review
  14. 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

4 authors.

Carole McArthurDepartment of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas, MO 64108, USA. McArthurC@umkc.edu.ORCID 0000-0002-9286-8362
Fabio GallazziBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA. gallazzif@missouri.edu.
Thomas P QuinnDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, USA. QuinnT@missouri.edu.
Kamal SinghBond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA. singhka@missouri.edu.ORCID 0000-0001-6153-8929

Funding

Reverse Transcriptase Multi-Class Drug Resistance and Rilpivirine Susceptibility in Diverse HIV-1 SubtypesR01GM118012 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI SARAFIANOS, STEFAN G · 2016 to 2019
$1.6M
NIGMS NIH HHS GM118012
6 · The paper itself

Abstract

Human immunodeficiency virus (HIV) capsid plays important roles at multiple stages of viral replication. At the initial stages, controlled uncoating (disassembly) of the capsid ensures efficient reverse transcription of the single-stranded RNA genome, into the double-stranded DNA. Whereas at later stages, a proper assembly of capsid ensures the formation of a mature infectious virus particle. Hence, the inhibition of capsid assembly and/or disassembly has been recognized as a potential therapeutic strategy, and several capsid inhibitors have been reported. Of these, PF-3450074 (PF74) has been extensively studied. Recently reported GS-CA inhibitors (GS-CA1 and GS-6207), have shown a strong potential and appear to contain a PF74 scaffold. The location of resistance mutations and the results of structural studies further suggest that GS-CA compounds and PF74 share the same binding pocket, which is located between capsid monomers. Additionally, phenylalanine derivatives containing the PF74 scaffold show slightly enhanced capsid inhibiting activity. A comparison of capsid structures in complex with host factors and PF74, reveals the presence of common chemical entities at topologically equivalent positions. Here we present the status of capsid inhibitors that contain PF74 scaffolds and propose that the PF74 scaffold may be used to develop strong and safe capsid inhibitors.

Indexed as

assemblycapsiddisassemblyGS-6207GS-CA1human immunodeficiency virusPF74small molecule inhibitorsuncoating

Identifiers

PMID31671622
PMCPMC6956309

What OpenQuestion holds

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LicenceCC BY
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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.