Evidence map›Paper›PMID 31105169›Full record

ArticleBiomimetics (Basel, Switzerland)2017

Catechol-Containing Hydroxylated Biomimetic 4-Thiaflavanes as Inhibitors of Amyloid Aggregation.

Matteo Ramazzotti, Paolo Paoli, Bruno Tiribilli, Caterina Viglianisi, Stefano Menichetti, Donatella Degl'innocenti

Open access · goldAbstract read
In one paragraph

Article in Biomimetics (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Matteo RamazzottiDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Università degli Studi di Firenze, viale G.B. Morgagni 50, 50134 Firenze, Italy. matteo.ramazzotti@unifi.it.ORCID 0000-0002-6862-9409
Paolo PaoliDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Università degli Studi di Firenze, viale G.B. Morgagni 50, 50134 Firenze, Italy. paolo.paoli@unifi.it.
Bruno TiribilliConsiglio Nazionale delle Ricerche (CNR), Istituto dei Sistemi Complessi, Via Madonna del Piano, 10, 50019 Sesto Fiorentino, Firenze, Italy. bruno.tiribilli@isc.cnr.it.ORCID 0000-0001-9851-1850
Caterina ViglianisiDipartimento di Chimica "Ugo Schiff", Polo Scientifico e Tecnologico, Università degli Studi di Firenze, via della Lastruccia 3-13, 50019 Sesto Fiorentino, Firenze, Italy. caterina.viglianisi@unifi.it.ORCID 0000-0002-2451-5856
Stefano MenichettiDipartimento di Chimica "Ugo Schiff", Polo Scientifico e Tecnologico, Università degli Studi di Firenze, via della Lastruccia 3-13, 50019 Sesto Fiorentino, Firenze, Italy. stefano.menichetti@unifi.it.ORCID 0000-0001-6745-7484
Donatella Degl'innocentiDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Università degli Studi di Firenze, viale G.B. Morgagni 50, 50134 Firenze, Italy. donatella.deglinnocenti@unifi.it.
University of Florence · ITInstitute for Complex Systems · IT

Funding

University of Florence Fondi di Ateneo 2015
6 · The paper itself

Abstract

The study of compounds able to interfere in various ways with amyloid aggregation is of paramount importance in amyloid research. Molecules characterized by a 4-thiaflavane skeleton have received great attention in chemical, medicinal, and pharmaceutical research. Such molecules, especially polyhydroxylated 4-thiaflavanes, can be considered as structural mimickers of several natural polyphenols that have been previously demonstrated to bind and impair amyloid fibril formation. In this work, we tested five different 4-thiaflavanes on the hen egg-white lysozyme (HEWL) amyloid model for their potential anti-amyloid properties. By combining a thioflavin T assay, atomic force microscopy, and a cell toxicity assay, we demonstrated that such compounds can impair the formation of high-order amyloid aggregates and mature fibrils. Despite this, the tested 4-thiaflavanes, although non-toxic per se, are not able to prevent amyloid toxicity on human neuroblastoma cells. Rather, they proved to block early aggregates in a stable, toxic conformation. Accordingly, 4-thiaflavanes can be proposed for further studies aimed at identifying blocking agents for the study of toxicity mechanisms of amyloid aggregation.

Indexed as

amyloid aggregationantioxidant activitycatecholhen egg white lysozymehydroxylated 4-thiaflavanesinhibition

Identifiers

PMID31105169
PMCPMC6477597
OpenAlexW2613601658

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.