Evidence map›Paper›PMID 41373859›Full record

ArticleInternational journal of molecular sciences2025

5-Substituted 4-Thiouridines, 4-Thio-2'-deoxyuridines and Their Oligoglycol Carbonate Prodrugs as Promising Antimicrobial Agents.

Dmitry A Makarov, Maxim V Jasko, Sergey D Negrya, Inna L Karpenko, Elizabeth V Urbina, Vladimir O Chekhov, Olga V Efremenkova, Byazilya F Vasilyeva, Danila V Zimenkov, Anastasia I Ushtanit and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Dmitry A MakarovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0003-2438-1146
Maxim V JaskoEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0003-0462-8930
Sergey D NegryaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-2885-8442
Inna L KarpenkoEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0001-9849-0447
Elizabeth V UrbinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0009-0000-7587-7526
Vladimir O ChekhovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0003-1247-9517
Olga V EfremenkovaGause Institute of New Antibiotics, 119021 Moscow, Russia.ORCID 0000-0003-3131-1031
Byazilya F VasilyevaGause Institute of New Antibiotics, 119021 Moscow, Russia.ORCID 0000-0001-9077-1965
Danila V ZimenkovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-2040-0904
Anastasia I UshtanitEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-7935-4316
Sergey N KochetkovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-7443-6961
Liudmila A AlexandrovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.

Funding

Russian Science Foundation 23-14-00106
6 · The paper itself

Abstract

The problem of antibiotic resistance is one of the challenges that science and medicine face in the 21st century. Nucleoside analogs have already proven as antiviral and antitumor agents, and, currently, there are more and more reports on their antibacterial and antifungal activity. The substitution of an oxygen atom by a sulfur one leads to the emergence of unique properties. Here, we report the synthesis of eight new 4-thioanalogs of 5-substituted (5-alkyloxymethyl and 5-alkyltriazolylmethyl) derivatives of 2'-deoxyuridine and uridine, which were active against

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsCarbonatesProdrugsThiouridineMicrobial Sensitivity TestsMycobacterium smegmatisMycobacterium tuberculosisUridineAnti-Bacterial AgentsAnti-Infective AgentsCarbonatesProdrugsThiouridineUridine5-substituted 4-thionucleosidesantibacterial activitymycobacterianucleosides

Identifiers

PMID41373859
PMCPMC12692488

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Registered trials

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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.