Evidence map›Paper›PMID 38505325›Full record

ArticleEuropean journal of organic chemistry2023

Fluorinated Analogues to the Pentuloses of the Pentose Phosphate Pathway.

Lukas Scheibelberger, Toda Stankovic, Kaja Liepert, Andreas Kienzle, Eva-Maria Patronas, Theresa Balber, Markus Mitterhauser, Arvand Haschemi, Katharina Pallitsch

Open access · hybridAbstract read
In one paragraph

Article in European journal of organic chemistry, 2023. 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
0.4field-weighted citation impact, top 35% 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. Design, Synthesis, andACS omega · 2024
    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

9 authors at 3 institutions in 1 country.

Lukas ScheibelbergerInstitute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.
Toda StankovicInstitute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.
Kaja LiepertInstitute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.
Andreas KienzleInstitute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.
Eva-Maria PatronasDivision of Nuclear Medicine Department of Biomedical Imaging and Image-guided Therapy Medical University of Vienna Währinger Gürtel 18-20 1090 Vienna Austria.
Theresa BalberDivision of Nuclear Medicine Department of Biomedical Imaging and Image-guided Therapy Medical University of Vienna Währinger Gürtel 18-20 1090 Vienna Austria.
Markus MitterhauserDivision of Nuclear Medicine Department of Biomedical Imaging and Image-guided Therapy Medical University of Vienna Währinger Gürtel 18-20 1090 Vienna Austria.
Arvand HaschemiDepartment of Laboratory Medicine Medical University of Vienna Währinger Gürtel 18-20 1090 Vienna Austria.
Katharina PallitschInstitute of Organic Chemistry University of Vienna Währinger Straße 38 1090 Vienna Austria.ORCID 0000-0003-2648-1044
University of Vienna · ATMedical University of Vienna · ATLudwig Boltzmann Institute Applied Diagnostics · AT

Funding

Austrian Science Fund FWF P 32421
6 · The paper itself

Abstract

Fluorinated carbohydrates are valuable tools for enzymological studies due to their increased metabolic stability compared to their non-fluorinated analogues. Replacing different hydroxyl groups within the same monosaccharide by fluorine allows to influence a wide range of sugar-receptor interactions and enzymatic transformations. In the past, this principle was frequently used to study the metabolism of highly abundant carbohydrates, while the metabolic fate of rare sugars is still poorly studied. Rare sugars, however, are key intermediates of many metabolic routes, such as the pentose phosphate pathway (PPP). Here we present the design and purely chemical synthesis of a set of three deoxyfluorinated analogues of the rare sugars d-xylulose and d-ribulose: 1-deoxy-1-fluoro-d-ribulose (

Indexed as

deoxyfluorinated carbohydratesd-Ribulosed-Xylulosepentose-phosphate-pathwayrare sugars

Identifiers

PMID38505325
PMCPMC10946780
OpenAlexW4377088228

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.