Evidence map›Paper›PMID 39140451›Full record

ArticleChemMedChem2024

Developing Allosteric Inhibitors of SARS-CoV-2 RNA-Dependent RNA Polymerase.

Artem Chayka, Matěj Danda, Alžběta Dostálková, Vojtěch Spiwok, Anna Klimešová, Marina Kapisheva, Michala Zgarbová, Jan Weber, Tomáš Ruml, Michaela Rumlová and 1 more

Abstract read
In one paragraph

Article in ChemMedChem, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Artem ChaykaInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, 16000, Prague 6, Czech Republic.
Matěj DandaDepartment of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Alžběta DostálkováDepartment of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Vojtěch SpiwokDepartment of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Anna KlimešováDepartment of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Marina KapishevaDepartment of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Michala ZgarbováInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, 16000, Prague 6, Czech Republic.
Jan WeberInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, 16000, Prague 6, Czech Republic.
Tomáš RumlDepartment of Biochemistry and Microbiology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Michaela RumlováDepartment of Biotechnology, University of Chemistry and Technology, Prague, Technická 5, 16628, Prague 6, Czech Republic.
Zlatko JanebaInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, 16000, Prague 6, Czech Republic.ORCID 0000-0003-4654-679X

Funding

Czech Science Foundation 22-17118SEuropean Union-Next Generation EUInstitute of Organic Chemistry and Biochemistry (RVO 61388963National Institute of virology and bacteriologyProgramme EXCELES LX22NPO5103
6 · The paper itself

Abstract

The use of Fpocket and virtual screening techniques enabled us to identify potential allosteric druggable pockets within the SARS-CoV-2 RNA-dependent RNA polymerase (RdRp). Of the compounds screened, compound 1 was identified as a promising inhibitor, lowering a SARS-CoV-2 RdRp activity to 57 % in an enzymatic assay at 10 μM concentration. The structure of compound 1 was subsequently optimized in order to preserve or enhance inhibitory activity. This involved the substitution of problematic ester and aromatic nitro groups with more inert functionalities. The N,N'-diphenylurea scaffold with two NH groups was identified as essential for the compound's activity but also exhibited high toxicity in Calu-3 cells. To address this issue, a scaffold hopping approach was employed to replace the urea core with potentially less toxic urea isosteres. This approach yielded several structural analogues with notable activity, specifically 2,2'-bisimidazol (in compound 55 with residual activity RA=42 %) and (1H-imidazol-2-yl)urea (in compounds 59 and 60, with RA=50 and 28 %, respectively). Despite these advances, toxicity remained a major concern. These compounds represent a promising starting point for further structure-activity relationship studies of allosteric inhibitors of SARS-CoV-2 RdRp, with the goal of reducing their cytotoxicity and improving aqueous solubility.

Indexed as

Antiviral AgentsSARS-CoV-2Allosteric RegulationCoronavirus RNA-Dependent RNA PolymeraseEnzyme InhibitorsHumansMolecular Docking SimulationMolecular StructureRNA-Dependent RNA PolymeraseStructure-Activity RelationshipAntiviral AgentsCoronavirus RNA-Dependent RNA PolymeraseEnzyme InhibitorsRNA-Dependent RNA Polymeraseallosteric inhibitorRdRp; remdesivirSARS-CoV-2SAR studyscaffold hopping

Identifiers

PMID39140451
PMCPMC11617668

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.