Evidence map›Paper›PMID 42794450›Full record

ReviewInternational journal of molecular sciences2026

Structural Modification of Resveratrol: Biological Activities and Anticancer Potential of Emerging Methoxylated Analogs.

Yashvi Sethia, Edyta Kopera, Jacek Tabarkiewicz

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 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

3 authors.

Yashvi SethiaStudents' Scientific Club at Department of Human Immunology, Faculty of Medicine, College for Medical Sciences, University of Rzeszów, 35-959 Rzeszów, Poland.ORCID 0009-0004-0493-4908
Edyta KoperaDepartment of Human Immunology, Faculty of Medicine, College for Medical Sciences, University of Rzeszów, 35-959 Rzeszów, Poland.
Jacek TabarkiewiczDepartment of Human Immunology, Faculty of Medicine, College for Medical Sciences, University of Rzeszów, 35-959 Rzeszów, Poland.ORCID 0000-0002-1264-2882

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resveratrol remains one of the most extensively studied plant-derived polyphenols because of its broad antioxidant, anti-inflammatory, cardioprotective, neuroprotective, and anticancer activities. However, its clinical translation has been substantially limited by its poor aqueous solubility, rapid phase II metabolism, and low systemic bioavailability, despite decades of intensive investigation. Structural modification through methoxylation has emerged as a promising strategy to overcome these pharmacokinetic limitations by enhancing metabolic stability, lipophilicity, membrane permeability, and biological activity. While considerable attention has focused on resveratrol and a limited number of established analogs, emerging methoxylated derivatives remain comparatively underexplored. This review highlights the structural characteristics, biological activities, and molecular mechanisms of two such derivatives, 4,4-(ethane-1,2-diyl)bis(2-methoxyphenol) (EG) and (

Indexed as

Antineoplastic AgentsAntineoplastic Agents, PhytogenicNeoplasmsResveratrolStilbenesAnimalsAntioxidantsHumansStructure-Activity Relationship3,4',5-trimethoxystilbeneAntineoplastic AgentsAntineoplastic Agents, PhytogenicAntioxidantsResveratrolStilbenes3,5,4′-trimethoxystilbene4,4′-(ethane-1,2-diyl)bis(2-methoxyphenol)anticancerantioxidantbioactiveplant-derivedresveratrol derivative

Identifiers

PMID42794450
PMCPMC13606549

What OpenQuestion holds

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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.