Evidence map›Paper›PMID 35542595›Full record

ArticleRSC advances2018

Atypical antioxidant activity of non-phenolic amino-coumarins.

Daniel Zúñiga-Núñez, Pablo Barrias, Gloria Cárdenas-Jirón, M Soledad Ureta-Zañartu, Camilo Lopez-Alarcón, F Eduardo Morán Vieyra, Claudio D Borsarelli, Emilio I Alarcon, Alexis Aspée

Abstract read
In one paragraph

Article in RSC advances, 2018. 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
–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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Antibacterial and Antioxidant Activities, Toxicity, and Physicochemical Properties ofAdvances in pharmacological and pharmaceutical sciences · 2024
    Article
  5. Article
  6. 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

9 authors.

Daniel Zúñiga-NúñezFacultad de Química y Biología, Universidad de Santiago de Chile (USACH) Casilla 40, Correo 33 Santiago Chile alexis.aspee@usach.cl.ORCID https://orcid.org/0000-0001-9967-1653
Pablo BarriasFacultad de Química y Biología, Universidad de Santiago de Chile (USACH) Casilla 40, Correo 33 Santiago Chile alexis.aspee@usach.cl.ORCID https://orcid.org/0000-0003-4072-4436
Gloria Cárdenas-JirónFacultad de Química y Biología, Universidad de Santiago de Chile (USACH) Casilla 40, Correo 33 Santiago Chile alexis.aspee@usach.cl.
M Soledad Ureta-ZañartuFacultad de Química y Biología, Universidad de Santiago de Chile (USACH) Casilla 40, Correo 33 Santiago Chile alexis.aspee@usach.cl.
Camilo Lopez-AlarcónDepartamento de Química Física, Facultad de Química, Pontificia Universidad Católica de Chile Av. Vicuña Mackenna 4860 Santiago Macul Chile.
F Eduardo Morán VieyraInstituto de Bionanotecnología del NOA (INBIONATEC), Universidad Nacional de Santiago del Estero (UNSE) CONICET. RN9, km 1125 CP4206 Santiago del Estero Argentina.
Claudio D BorsarelliInstituto de Bionanotecnología del NOA (INBIONATEC), Universidad Nacional de Santiago del Estero (UNSE) CONICET. RN9, km 1125 CP4206 Santiago del Estero Argentina.
Emilio I AlarconBio-nanomaterials Chemistry and Engineering Laboratory, Division of Cardiac Surgery, University of Ottawa Heart Institute 40 Ruskin St. Ottawa Ontario K1Y 4W7 Canada.ORCID https://orcid.org/0000-0001-5100-6179
Alexis AspéeFacultad de Química y Biología, Universidad de Santiago de Chile (USACH) Casilla 40, Correo 33 Santiago Chile alexis.aspee@usach.cl.ORCID https://orcid.org/0000-0001-5554-6877

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coumarin compounds have been described as anti-inflammatories, and chemotherapeutic agents as well as antioxidants. However, the origin of the antioxidant activity of non phenolic coumarins remains obscure. In the present report, we demonstrate that non-phenolic 7-dialkyl-aminocoumarins may also have significant antioxidant properties against free radicals derived from 2,2'-azobis(2-amidinopropane) dihydrochloride under aerobic conditions. This atypical behaviour is due to the presence of traces of very reactive hydroxycinnamic acid-type compounds. Changing functional groups at the C-3 and C-4 positions shifts the reactivity of the compounds from peroxyl to alkoxyl free radicals. Kinetic and theoretical studies based on Density Functional Theory support the formation of reactive hydroxycinnamic acid and directly link the antioxidant behaviour of the compounds to hydrogen atom transfer.

Identifiers

PMID35542595
PMCPMC9077249

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.