Evidence map›Paper›PMID 33432805›Full record

ArticleBiomacromolecules2021

Sulfated Oligomers of Tyrosol: Toward a New Class of Bioinspired Nonsaccharidic Anticoagulants.

Maria Laura Alfieri, Lucia Panzella, Bárbara Duarte, Salomé Gonçalves-Monteiro, Franklim Marques, Manuela Morato, Marta Correia-da-Silva, Luisella Verotta, Alessandra Napolitano

Open access · hybridAbstract read
In one paragraph

Article in Biomacromolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

9 authors at 3 institutions in 2 countries.

Maria Laura AlfieriDepartment of Chemical Sciences, University of Naples Federico II, I-80126 Naples, Italy.
Lucia PanzellaDepartment of Chemical Sciences, University of Naples Federico II, I-80126 Naples, Italy.ORCID 0000-0002-2662-8205
Bárbara DuarteUCIBIO/REQUIMTE and Clinical Analysis Unit, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Salomé Gonçalves-MonteiroLAQV/REQUIMTE and Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Franklim MarquesUCIBIO/REQUIMTE and Clinical Analysis Unit, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Manuela MoratoLAQV/REQUIMTE and Laboratory of Pharmacology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Marta Correia-da-SilvaCIIMAR and Laboratory of Organic and Pharmaceutical Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0003-4150-8532
Luisella VerottaDepartment of Environmental Science and Policy, University of Milan, 20133 Milano, Italy.
Alessandra NapolitanoDepartment of Chemical Sciences, University of Naples Federico II, I-80126 Naples, Italy.ORCID 0000-0003-0507-5370
Universidade do Porto · PTUniversity of Naples Federico II · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sulfated phenolic polymers have extensively been investigated as anticoagulant agents in view of their higher bioavailability and resistance to degradation compared to heparins, allowing for increased half-lives. In this frame, we report herein the preparation of sulfated derivatives of tyrosol, one of the most representative phenolic constituents of extra virgin olive oil, by different approaches. Mild sulfation of OligoTyr, a mixture of tyrosol oligomers, that has been reported to possess antioxidant properties and osteogenic activity, afforded OligoTyrS I in good yields. Elemental analysis, NMR, and MALDI-MS investigation provided evidence for an almost complete sulfation at the OH on the phenylethyl chain, leaving the phenolic OH free. Peroxidase/H

Indexed as

AnticoagulantsSulfatesAnimalsHeparinHydrogen PeroxideMicePartial Thromboplastin TimePhenylethyl Alcohol4-hydroxyphenylethanolAnticoagulantsHeparinHydrogen PeroxidePhenylethyl AlcoholSulfates

Identifiers

PMID33432805
PMCPMC8023584
OpenAlexW3119492673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.