Evidence mapPaperPMID 42198331Full record

ReviewPharmaceuticals (Basel, Switzerland)2026

Glucosinolate Derivatives: Emerging Anti-Inflammatory Agents.

Sandrine Ressurreição, Sónia A Pinho, Maria Teresa Cruz, Lígia Salgueiro, Artur Figueirinha

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 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.

Sandrine RessurreiçãoUniversity of Coimbra, Faculty of Pharmacy, 3000-548 Coimbra, Portugal.ORCID 0000-0002-1596-8722
Sónia A PinhoUniversity of Coimbra, Faculty of Pharmacy, 3000-548 Coimbra, Portugal.ORCID 0000-0002-7426-5197
Maria Teresa CruzUniversity of Coimbra, Faculty of Pharmacy, 3000-548 Coimbra, Portugal.ORCID 0000-0001-9846-6754
Lígia SalgueiroUniversity of Coimbra, Faculty of Pharmacy, 3000-548 Coimbra, Portugal.ORCID 0000-0003-0948-821X
Artur FigueirinhaUniversity of Coimbra, Faculty of Pharmacy, 3000-548 Coimbra, Portugal.ORCID 0000-0003-3064-5718

Funding

European Union's Horizon Europe programme project 101080329Foundation for Science and Technology (FCT/MCTES) 10.54499/LA/P/0058/2020Foundation for Science and Technology (FCT/MCTES) 10.54499/UID/00102/2025Foundation for Science and Technology (FCT/MCTES) 10.54499/UID/50006/2025Foundation for Science and Technology (FCT/MCTES) 10.54499/UIDP/04539/2020Foundation for Science and Technology (FCT/MCTES) 10.54499/UID/PRR/00102/2025Foundation for Science and Technology (FCT/MCTES) 10.54499/UID/PRR/04539/2025Foundation for Science and Technology (FCT/MCTES) 10.54499/UID/PRR/50006/2025
6 · The paper itself

Abstract

Glucosinolates are sulfur-containing secondary metabolites predominantly found in Brassicaceae plants, which, upon enzymatic hydrolysis, generate bioactive compounds with potent anti-inflammatory properties. These derivatives modulate key inflammatory pathways by inhibiting NF-κB nuclear translocation, reducing pro-inflammatory cytokine production, including TNF-α, IL-6, and IL-1β, and suppressing iNOS and COX-2 expressions. They also activate NRF2-dependent antioxidant defenses, upregulating enzymes such as HO-1 and NQO1, and regulate MMPs, contributing to tissue protection during chronic inflammation. Evidence from in vitro and in vivo studies consistently demonstrates their ability to attenuate inflammation and oxidative stress. Although approximately 137 glucosinolates have been identified, only about twelve have been investigated in detail regarding the anti-inflammatory activity of their derivatives, highlighting a significant gap in current knowledge and considerable potential for the discovery of new therapeutic compounds. In this context, a systematic survey was conducted of plant species reported in scientific literature as sources of glucosinolates, with particular emphasis on studies evaluating their extracts and fractions for anti-inflammatory potential in in vitro and in vivo experimental models. Additionally, this review also aims to highlight the anti-inflammatory and antioxidant potential of glucosinolate-derived compounds, focusing on their modulation of the NF-κB and NRF2 signaling pathways and their ability to regulate matrix metalloproteinases. It also emphasizes that, despite the broad diversity of glucosinolates identified to date, only a limited number have been functionally investigated. By addressing this gap, and based on the systematic survey performed, this review underscores the need for further research to fully explore their therapeutic potential.

Indexed as

anti-inflammatory activityglucosinolate derivatesMMPsNF-κBNRF2

Identifiers

PMID42198331
PMCPMC13209208

What Socratic holds

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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 Socratic graph.