Evidence map›Paper›PMID 36950082›Full record

ReviewRSC advances2023

KuQuinones: a ten years tale of the new pentacyclic quinoid compound.

Francesca Valentini, Federica Sabuzi, Mattia Forchetta, Valeria Conte, Pierluca Galloni

Abstract readReview
In one paragraph

Review in RSC advances, 2023. 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
–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

4 citing papers in PubMed.

  1. Fluorination of amino-quinones enhances anti-RSC medicinal chemistry · 2026
    Article
  2. Article
  3. Article
  4. 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

5 authors.

Francesca ValentiniDepartment of Chemical Science and Technologies, University of Rome Tor Vergata via della ricerca scientifica snc 00133 Rome Italy galloni@scienze.uniroma2.it.ORCID https://orcid.org/0000-0003-3371-589X
Federica SabuziDepartment of Chemical Science and Technologies, University of Rome Tor Vergata via della ricerca scientifica snc 00133 Rome Italy galloni@scienze.uniroma2.it.
Mattia ForchettaDepartment of Chemical Science and Technologies, University of Rome Tor Vergata via della ricerca scientifica snc 00133 Rome Italy galloni@scienze.uniroma2.it.
Valeria ConteDepartment of Chemical Science and Technologies, University of Rome Tor Vergata via della ricerca scientifica snc 00133 Rome Italy galloni@scienze.uniroma2.it.
Pierluca GalloniDepartment of Chemical Science and Technologies, University of Rome Tor Vergata via della ricerca scientifica snc 00133 Rome Italy galloni@scienze.uniroma2.it.ORCID https://orcid.org/0000-0002-0941-1354

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quinones are widespread in nature, as they participate, mainly as redox mediators, in several biochemical processes. Up to now, various synthetic quinones have been recommended in the literature as leading molecules in energy, biomedical and catalytic fields. In this brief review, we retraced our research activity in the last ten years, mainly dedicated to the study of a new class of peculiar pentacyclic conjugated quinoid compounds, synthesized in our group. In particular, their application as sensitive materials in photoelectrochemical devices and in biosensors, as photocatalysts in selective oxidation reactions, and their anticancer activity is here reviewed.

Identifiers

PMID36950082
PMCPMC10025941

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.