Evidence map›Paper›PMID 41913092›Full record

ArticleChemMedChem2026

Functionalized Cyclic Beta-Amino Acid Derivatives With Antiviral Potential.

Melinda Nonn, Marta Denel-Bobrowska, Balázs Volk, Agnieszka B Olejniczak, Loránd Kiss

Abstract read
In one paragraph

Article in ChemMedChem, 2026. 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

5 authors.

Melinda NonnMTA TTK Lendület Artificial Transporter Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Center for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Marta Denel-BobrowskaInstitute of Medical Biology, Polish Academy of Sciences, Łódź, Poland.
Balázs VolkEgis Pharmaceuticals Plc., Directorate of Drug Substance Development, Budapest, Hungary.
Agnieszka B OlejniczakInstitute of Medical Biology, Polish Academy of Sciences, Łódź, Poland.ORCID https://orcid.org/0000-0003-4628-9017
Loránd KissInstitute of Organic Chemistry, Stereochemistry Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.ORCID https://orcid.org/0000-0003-2346-9816

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selected highly functionalized cyclic beta (β)-amino acid derivatives have been synthesized according to modified and improved literature synthetic protocols and subjected to various antiviral studies. The model compounds were regio- and stereoisomers of azido-functionalized β-amino esters, orthogonally protected diamino esters, an oxirane-fused cyclic β-amino ester, 1,2,3-triazole-substituted β-amino esters, mono- and difluorinated cyclic β-amino esters, mono and dihydroxylated cyclic β-amino esters, dihydroxylated lactams, and β-amino esters with piperidine and azepane skeletons. Formed compounds have been investigated and their anti-HCMV (Human cytomegalovirus), anti-HRV8 (Human rhinovirus 8), and anti-HSV-1 (Human herpesvirus 1) activities were tested (CC50 and IC50 determinations) during screening studies.

Indexed as

Amino AcidsAmino Acids, CyclicAntiviral AgentsCytomegalovirusHerpesvirus 1, HumanHumansMicrobial Sensitivity TestsMolecular StructureRhinovirusStereoisomerismStructure-Activity RelationshipAmino AcidsAmino Acids, CyclicAntiviral Agentsantiviral propertycyclic amino acidsdrug designfunctionalizationstereocenter

Identifiers

PMID41913092
PMCPMC13035932

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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.