Evidence map›Paper›PMID 42636233›Full record

ArticlePloS one2026

A bioactivity-leveling approach for component-specific evaluation in natural product extracts: Optimizing SARS-CoV-2 antiviral screening by controlling for pheophorbide A.

Corinna Urmann, Yvonne Gmach, Niklas Hofer, Nina Vahekeni, Jonas Stehlin, Yannick Geissmann, Andreas Lardos, Olivier Engler, Evelyn Wolfram

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Corinna UrmannOrganic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, Straubing, Germany.ORCID https://orcid.org/0000-0001-8895-9416
Yvonne GmachOrganic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, Straubing, Germany.
Niklas HoferOrganic-analytical Chemistry, Weihenstephan-Triesdorf University of Applied Sciences, Straubing, Germany.ORCID https://orcid.org/0009-0008-1429-6865
Nina VahekeniNatural Product Chemistry and Phytopharmacy Group, Institute of Chemistry and Biotechnology, School of Life Sciences and Facility Management, ZHAW Zurich University of Applied Sciences, Wädenswil, Switzerland.
Jonas StehlinNatural Product Chemistry and Phytopharmacy Group, Institute of Chemistry and Biotechnology, School of Life Sciences and Facility Management, ZHAW Zurich University of Applied Sciences, Wädenswil, Switzerland.
Yannick GeissmannSpiez Laboratory, Federal Office for Civil Protection, Spiez, Switzerland.
Andreas LardosNatural Product Chemistry and Phytopharmacy Group, Institute of Chemistry and Biotechnology, School of Life Sciences and Facility Management, ZHAW Zurich University of Applied Sciences, Wädenswil, Switzerland.
Olivier EnglerSpiez Laboratory, Federal Office for Civil Protection, Spiez, Switzerland.
Evelyn WolframNatural Product Chemistry and Phytopharmacy Group, Institute of Chemistry and Biotechnology, School of Life Sciences and Facility Management, ZHAW Zurich University of Applied Sciences, Wädenswil, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of SARS-CoV-2 has intensified the search for novel antiviral agents, with plants representing a promising source due to the documented antiviral properties. Pheophorbides, chlorophyll breakdown products, have been demonstrated to impede viral entry of enveloped viruses. However, the frequent occurrence of pheophorbide A in plant extracts presents a challenge for antiviral screening, as it may obscure the discovery of novel antiviral compounds. The objective of this study was therefore leveling out the influence of pheophorbide A in an in vitro virus pretreatment assay, to prioritize extracts and fractions and support the identification of additional antiviral compounds in plant extracts. Using different experimental derived examples, the limitations and advantages of the strategy presented are discussed. Assay-derived protective effects were interpreted in relation to pheophorbide A quantification, allowing six out of 15 plant species to be prioritized for further investigations. Qualitative comparison of metabolite profiles of fractions with the extent of protective effect supported the prioritization process and led to the identification of candidate compounds potentially contributing to the observed protective effect in Primula veris L. beyond pheophorbide A. Overall, the results highlight the potential value of the proposed strategy for revealing bioactivity beyond known predominant effectors and suggest an applicability in natural product-based screening approaches.

Indexed as

Antiviral AgentsBiological ProductsChlorophyllPlant ExtractsSARS-CoV-2AnimalsChlorocebus aethiopsDrug Evaluation, PreclinicalHumansVero CellsAntiviral AgentsBiological ProductsChlorophyllpheophorbide aPlant Extracts

Identifiers

PMID42636233
PMCPMC13502696

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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.