Evidence map›Paper›PMID 38542941›Full record

ArticleMolecules (Basel, Switzerland)2024

Enzymatic Synthesis of New Acetoacetate-Ursodeoxycholic Acid Hybrids as Potential Therapeutic Agents and Useful Synthetic Scaffolds as Well.

Valentina Venturi, Elena Marchesi, Daniela Perrone, Valentina Costa, Martina Catani, Simona Aprile, Lindomar Alberto Lerin, Federico Zappaterra, Pier Paolo Giovannini, Lorenzo Preti

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. 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
1.7field-weighted citation impact, top 14% 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. Review
  2. Article
  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

10 authors at 1 institution in 1 country.

Valentina VenturiDepartment of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy.
Elena MarchesiDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0002-5402-4732
Daniela PerroneDepartment of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0001-5189-011X
Valentina CostaDepartment of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0001-8188-831X
Martina CataniDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0003-4217-8766
Simona AprileDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.
Lindomar Alberto LerinDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0001-7411-8974
Federico ZappaterraDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0001-5852-2942
Pier Paolo GiovanniniDepartment of Chemical Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy.
Lorenzo PretiDepartment of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0002-5912-998X
University of Ferrara · IT

Funding

National Recovery and Resilience Plan (NRRP) eu 0001052
6 · The paper itself

Abstract

Ursodeoxycholic acid (UDCA) and acetoacetate are natural compounds present in the human intestine and blood, respectively. A number of studies highlighted that besides their well-known primary biological roles, both compounds possess the ability to influence a variety of cellular processes involved in the etiology of various diseases. These reasons suggested the potential of acetoacetate-UDCA hybrids as possible therapeutic agents and prompted us to develop a synthetic strategy to selectively derivatize the hydroxyl groups of the bile acid with acetoacetyl moieties. 3α-acetoacetoxy UDCA was obtained (60% isolated yield) via the regioselective transesterification of methyl acetoacetate with UDCA promoted by the

Indexed as

AcetoacetatesUrsodeoxycholic AcidBile Acids and SaltsHumansAcetoacetatesacetoacetic acidBile Acids and Saltsmethyl acetoacetateUrsodeoxycholic Acidacetoacetatebiocatalysishybrid compoundsketone bodieslipaseursodeoxycholic acid

Identifiers

PMID38542941
PMCPMC10975173
OpenAlexW4392852430

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.