ArticlePrecision chemistry2026
Atomically Precise Polyanionic Boron Cluster Agents with Broad-Spectrum Antiviral Activity.
Article in Precision chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Influence of Spacer Chains Derived from Ring-Opened Crown Ethers on the Anti-Influenza A Virus Activity ofMolecules (Basel, Switzerland) · 2026Article
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Authors and funding
7 authors.
Funding
Abstract
The development of antivirals capable of addressing infections from multiple viruses is critically needed, as underscored by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic and ongoing annual influenza epidemics. Polyanionic polymer and hybrid gold nanoparticle (AuNP) systems have both previously shown significant infection inhibition activity against a wide variety of enveloped viruses. However, both of these systems exhibit variability in molecular weight and charge density distribution, which makes detailed structure-activity relationships difficult to ascertain. In this work, we report the synthesis of well-defined, dodecaborate-based clusters that are densely surface functionalized with charged ligands. These compounds exhibit minimal cytotoxic effects against mammalian cells, and several structures possess promising antiviral activity against both human immunodeficiency virus (HIV-1) and cytomegalovirus (CMV). This library of compounds offers a promising scaffold from which the roles of ligand identity, molecule size, and charge density on antiviral activity can be further studied and may ultimately help guide future design of antiviral agents.
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Registered trials
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