Evidence map›Paper›PMID 35195403›Full record

ArticleJournal of agricultural and food chemistry2022

Oxyresveratrol and Gnetol Glucuronide Metabolites: Chemical Production, Structural Identification, Metabolism by Human and Rat Liver Fractions, and

Ruth Hornedo-Ortega, Michaël Jourdes, Gregory Da Costa, Arnaud Courtois, Julien Gabaston, Pierre-Louis Teissedre, Tristan Richard, Stéphanie Krisa

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of agricultural and food chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
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  6. Review
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

8 authors at 1 institution in 1 country.

Ruth Hornedo-OrtegaUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.ORCID 0000-0003-1898-8806
Michaël JourdesUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.ORCID 0000-0002-5436-5238
Gregory Da CostaUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.
Arnaud CourtoisUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.
Julien GabastonUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.
Pierre-Louis TeissedreUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.
Tristan RichardUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.ORCID 0000-0002-5308-8697
Stéphanie KrisaUnité de Recherche Œnologie, Institut des Sciences de la Vigne et du Vin, Université de Bordeaux, EA 4577, USC 1366 INRA, IPB, 210 Chemin de Leysotte, CS 50008, 33882 Villenave d'Ornon Cedex, France.
Université de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stilbene metabolites are attracting great interest because many of them exhibit similar or even stronger biological effects than their parent compounds. Furthermore, the metabolized forms are predominant in biological fluids; therefore, their study is highly relevant. After hemisynthesis production, isolation, and structural elucidation, three glucuronide metabolites for oxyresveratrol (ORV) were formed:

Indexed as

GlucuronidesStilbenesAnimalsAnti-Inflammatory AgentsHumansInterleukin-1betaLipopolysaccharidesLiverNitric OxidePlant ExtractsRatsReactive Oxygen SpeciesTumor Necrosis Factor-alpha2,3',5',6-tetrahydroxy-trans-stilbeneAnti-Inflammatory AgentsGlucuronidesInterleukin-1betaLipopolysaccharidesNitric OxidePlant Extractspuag-haadReactive Oxygen SpeciesStilbenesTumor Necrosis Factor-alphaglucuronidehemisynthesisinflammationmetabolismstilbenes

Identifiers

PMID35195403
PMCPMC9585577
OpenAlexW4213287746

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.