Evidence map›Paper›PMID 34201477›Full record

ArticleInternational journal of molecular sciences2021

Influence of the Anthocyanin and Cofactor Structure on the Formation Efficiency of Naturally Derived Pyranoanthocyanins.

Gonzalo Miyagusuku-Cruzado, Danielle M Voss, M Monica Giusti

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Structure Elucidation of Purpurinidin fromJournal of natural products · 2025
    Article
  3. Article
  4. Article
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 at 1 institution in 1 country.

Gonzalo Miyagusuku-CruzadoDepartment of Food Science and Technology, The Ohio State University, 2015 Fyffe Rd., Columbus, OH 43210 1007, USA.ORCID 0000-0002-4420-6022
Danielle M VossDepartment of Food Science and Technology, The Ohio State University, 2015 Fyffe Rd., Columbus, OH 43210 1007, USA.ORCID 0000-0002-6128-6570
M Monica GiustiDepartment of Food Science and Technology, The Ohio State University, 2015 Fyffe Rd., Columbus, OH 43210 1007, USA.ORCID 0000-0002-2348-3530
The Ohio State University · US

Funding

Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica 225-2015-FONDECYTNational Institute of Food and Agriculture Hatch Project OHO01423 Accession Number 1014136
6 · The paper itself

Abstract

Pyranoanthocyanins are anthocyanin-derived pigments with higher stability to pH and storage. However, their slow formation and scarcity in nature hinder their industrial application. Pyranoanthocyanin formation can be accelerated by selecting anthocyanin substitutions, cofactor concentrations, and temperature. Limited information is available on the impacts of the chemical structure of the cofactor and anthocyanin; therefore, we evaluated their impacts on pyranoanthocyanin formation efficiency under conditions reported as favorable for the reaction. Different cofactors were evaluated including pyruvic acid, acetone, and hydroxycinnamic acids (

Indexed as

AcetoneAnthocyaninsBerberisCaffeic AcidsCoumaric AcidsGlycosidesMolecular StructurePyransPyruvic AcidAcetoneAnthocyaninscaffeic acidCaffeic AcidsCoumaric Acidscyanidin-3-glycosideGlycosidesmalvidinpetunidinPyransPyruvic Acidsinapinic acid10-catechyl-pyranoanthocyaninsaccelerated formationhydroxyphenyl-pyranoanthocyaninsnaturally derived pigments

Identifiers

PMID34201477
PMCPMC8268429
OpenAlexW3173842157

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.