Evidence map›Paper›PMID 39065650›Full record

ArticlePharmaceutics2024

Exploring a New Generation of Pyrimidine and Pyridine Derivatives as Anti-Influenza Agents Targeting the Polymerase PA-PB1 Subunits Interaction.

Ilaria Giacchello, Annarita Cianciusi, Chiara Bertagnin, Anna Bonomini, Valeria Francesconi, Mattia Mori, Anna Carbone, Francesca Musumeci, Arianna Loregian, Silvia Schenone

Abstract read
In one paragraph

Article in Pharmaceutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Ilaria GiacchelloDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.
Annarita CianciusiDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.
Chiara BertagninDepartment of Molecular Medicine, University of Padua, Via A. Gabelli 63, 35121 Padua, Italy.ORCID 0000-0003-2985-3392
Anna BonominiDepartment of Molecular Medicine, University of Padua, Via A. Gabelli 63, 35121 Padua, Italy.ORCID 0000-0001-9022-9551
Valeria FrancesconiDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.ORCID 0000-0002-1414-9266
Mattia MoriDepartment of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.ORCID 0000-0003-2398-1254
Anna CarboneDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.ORCID 0000-0002-6767-2376
Francesca MusumeciDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.ORCID 0000-0002-7228-0086
Arianna LoregianDepartment of Molecular Medicine, University of Padua, Via A. Gabelli 63, 35121 Padua, Italy.ORCID 0000-0002-8900-861X
Silvia SchenoneDepartment of Pharmacy, University of Genoa, Viale Benedetto XV 3, 16132 Genoa, Italy.

Funding

Fondazione Cassa di Risparmio di Padova e Rovigo, Italy 55777 2020.0162Italian Association for Cancer Research 25899Ministero dell'Università e della Ricerca (MUR), Italy with PRIN 2022 20223RYYFCMinistero dell'Università e della Ricerca (MUR), Italy with PRIN 2022 PNRR P20222YKP8NextGenerationEU-MUR PNRR PE00000007
6 · The paper itself

Abstract

The limited range of available flu treatments due to virus mutations and drug resistance have prompted the search for new therapies. RNA-dependent RNA polymerase (RdRp) is a heterotrimeric complex of three subunits, i.e., polymerase acidic protein (PA) and polymerase basic proteins 1 and 2 (PB1 and PB2). It is widely recognized as one of the most promising anti-flu targets because of its critical role in influenza infection and high amino acid conservation. In particular, the disruption of RdRp complex assembly through protein-protein interaction (PPI) inhibition has emerged as a valuable strategy for discovering a new therapy. Our group previously identified the 3-cyano-4,6-diphenyl-pyridine core as a privileged scaffold for developing PA-PB1 PPI inhibitors. Encouraged by these findings, we synthesized a small library of pyridine and pyrimidine derivatives decorated with a thio-N-(m-tolyl)acetamide side chain (compounds

Indexed as

antiviral agentsPA–PB1 inhibitorsprotein-protein interaction inhibitorsRdRpsmall molecules

Identifiers

PMID39065650
PMCPMC11279468

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.