Evidence map›Paper›PMID 30108738›Full record

ArticleMedChemComm2017

N-Heterocyclic borneol derivatives as inhibitors of Marburg virus glycoprotein-mediated VSIV pseudotype entry.

A A Kononova, A S Sokolova, S V Cheresiz, O I Yarovaya, R A Nikitina, A A Chepurnov, A G Pokrovsky, N F Salakhutdinov

Open access · hybridAbstract read
In one paragraph

Article in MedChemComm, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Pharmacological and bioactive properties ofFrontiers in pharmacology · 2025
    Review
  2. Molecules (Basel, Switzerland) · 2024
    Review
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  5. Synthesis of conjugates of (aRussian chemical bulletin = Izvestiia Akademii nauk. Seriia khimicheskaia · 2023
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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

8 authors at 3 institutions in 2 countries.

A A KononovaNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.
A S SokolovaNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.ORCID 0000-0001-5227-9996
S V CheresizNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.
O I YarovayaNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.ORCID 0000-0002-2333-4893
R A NikitinaScientific Research Institute of Clinical Immunology, Siberian Branch , Academy of Medical Sciences of Russia , Yadrintsevskaya St. 14 , 630099 , Novosibirsk , Russia.
A A ChepurnovScientific Research Institute of Clinical Immunology, Siberian Branch , Academy of Medical Sciences of Russia , Yadrintsevskaya St. 14 , 630099 , Novosibirsk , Russia.
A G PokrovskyNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.
N F SalakhutdinovNovosibirsk State University , Pirogova St. 2 , 630090 Novosibirsk , Russia . Email: ooo@nioch.nsc.ru.
Novosibirsk State University · RURussian Academy of Sciences · RUAcademy of Medical Sciences · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is currently no approved antiviral therapy for treatment of Marburg virus disease (MVD). Although filovirus infection outbreaks are quite rare, the high mortality rates in such outbreaks make the development of anti-filoviral drugs an important goal of medical chemistry and virology. Here, we performed screening of a large library of natural derivatives for their virus entry inhibition activity using pseudotype systems. The bornyl ester derivatives containing saturated N-heterocycles exhibited the highest antiviral activity. It is supposed that compounds with specific inhibitory activity toward MarV-GP-dependent virus entry will inhibit the rVSIV-ΔG-MarV-GP pseudotype much more efficiently than the control rVSIV-ΔG-G pseudotype. At the same time, the compounds similarly inhibiting both pseudotypes will likely affect rVSIV capsid replication or the cellular mechanisms common to the entry of both viruses. Borneol itself is not active against both pseudotypes and is nontoxic, whereas its derivatives have varying toxicity and antiviral activity. Among low-toxic borneol derivatives, six compounds turned out to be relatively specific inhibitors of MarV-GP-mediated infection (SC > 10). Of them, compound

Identifiers

PMID30108738
PMCPMC6072471
OpenAlexW2767169458

What OpenQuestion holds

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LicenceCC BY-NC
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.