Evidence map›Paper›PMID 39334821›Full record

ArticleBiomolecules2024

Synthesis and Biological Profiling of Seven Heparin and Heparan Sulphate Analogue Trisaccharides.

Fruzsina Demeter, Zsófia Peleskei, Katalin Kútvölgyi, Ágnes Rusznyák, Ferenc Fenyvesi, Richárd Kajtár, Éva Sipos, István Lekli, Petra Molnár, Attila Gábor Szöllősi and 4 more

Abstract read
In one paragraph

Article in Biomolecules, 2024. 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. Article
  2. 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

14 authors.

Fruzsina DemeterDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Zsófia PeleskeiDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Katalin KútvölgyiDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Ágnes RusznyákDepartment of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Nagyerdei Körút 98, H-4032 Debrecen, Hungary.ORCID 0000-0002-8837-7499
Ferenc FenyvesiDepartment of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Nagyerdei Körút 98, H-4032 Debrecen, Hungary.ORCID 0000-0003-2890-0783
Richárd KajtárDepartment of Pharmacodynamics, Faculty of Pharmacy, University of Debrecen, Nagyerdei Körút 98, H-4032 Debrecen, Hungary.
Éva SiposDepartment of Pharmacodynamics, Faculty of Pharmacy, University of Debrecen, Nagyerdei Körút 98, H-4032 Debrecen, Hungary.
István LekliDepartment of Pharmacodynamics, Faculty of Pharmacy, University of Debrecen, Nagyerdei Körút 98, H-4032 Debrecen, Hungary.ORCID 0000-0002-0992-4176
Petra MolnárDepartment of Immunology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Attila Gábor SzöllősiDepartment of Immunology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0001-6046-8236
Erika LisztesDepartment of Physiology, University of Debrecen, P.O. Box 22, H-4012 Debrecen, Hungary.
Balázs István TóthDepartment of Physiology, University of Debrecen, P.O. Box 22, H-4012 Debrecen, Hungary.ORCID 0000-0002-4103-4333
Anikó BorbásDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0001-8462-4547
Mihály HerczegDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0002-7938-9789

Funding

National Research and Development and Innovation Office of Hungary FK 134725National Research and Development and Innovation Office of Hungary FK 137924National Research and Development and Innovation Office of Hungary PD 134791New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund ÚNKP-23-4University of Debrecen Program for Scientific Publication
6 · The paper itself

Abstract

Researchers are paying increasing attention to the strongly negatively charged heteropolysaccharides in cells, in the extracellular matrix or in the cell wall. Examples of such molecules are glycosaminoglycans (e.g., heparin, heparan sulphate). It is well known from the literature that heparin and its derivatives have anti-inflammatory, angiogenic, metastatic and growth factor inhibitory activity. Herein, we present the efficient synthesis of six non-glycosaminoglycan (Glc-GlcA-Glc-sequenced) and one heparin-related (GlcN-GlcA-Glc-sequenced) trisaccharides with various functional group patterns. The anti-inflammatory, antioxidant and cell growth-inhibitory/cytotoxic effects of the synthesized compounds were tested. Among the investigated molecules, we have found some derivatives with a promising anti-inflammatory and antioxidant effect.

Indexed as

AntioxidantsHeparan SulfateHeparinTrisaccharidesAnimalsAnti-Inflammatory AgentsHumansMiceAnti-Inflammatory AgentsAntioxidantsHeparan SulfateHeparinTrisaccharidesanti-inflammatoryantioxidantheparan sulphateheparintrisaccharides

Identifiers

PMID39334821
PMCPMC11429564

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.