Evidence map›Paper›PMID 39062466›Full record

ArticleBiomolecules2024

Synthesis of Chiral Acyclic Pyrimidine Nucleoside Analogues from DHAP-Dependent Aldolases.

Mariano Nigro, Israél Sánchez-Moreno, Raúl Benito-Arenas, Ana L Valino, Adolfo M Iribarren, Nicolás Veiga, Eduardo García-Junceda, Elizabeth S Lewkowicz

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Mariano NigroLaboratorio de Biotransformaciones y Química de Ácidos Nucleicos, Universidad Nacional de Quilmes, Bernal 1876, Argentina.
Israél Sánchez-MorenoDepartamento de Química Bio-Orgánica, Instituto de Química Orgánica General, Consejo Superior de Investigaciones Científicas, 28006 Madrid, Spain.
Raúl Benito-ArenasDepartamento de Química Bio-Orgánica, Instituto de Química Orgánica General, Consejo Superior de Investigaciones Científicas, 28006 Madrid, Spain.ORCID 0000-0002-5651-8779
Ana L ValinoLaboratorio de Biotransformaciones y Química de Ácidos Nucleicos, Universidad Nacional de Quilmes, Bernal 1876, Argentina.
Adolfo M IribarrenLaboratorio de Biotransformaciones y Química de Ácidos Nucleicos, Universidad Nacional de Quilmes, Bernal 1876, Argentina.
Nicolás VeigaQuímica Inorgánica, Departamento Estrella Campos, Facultad de Química, Universidad de la República (UdelaR), Av. Gral. Flores 2124, Montevideo 11800, Uruguay.ORCID 0000-0001-8552-058X
Eduardo García-JuncedaDepartamento de Química Bio-Orgánica, Instituto de Química Orgánica General, Consejo Superior de Investigaciones Científicas, 28006 Madrid, Spain.ORCID 0000-0002-2344-8743
Elizabeth S LewkowiczLaboratorio de Biotransformaciones y Química de Ácidos Nucleicos, Universidad Nacional de Quilmes, Bernal 1876, Argentina.ORCID 0000-0002-5563-6271

Funding

ANPCyT PICTuniversidad nacional de Quilmes EXPTE. 2287/22
6 · The paper itself

Abstract

Dihydroxyacetone phosphate (DHAP)-dependent aldolases catalyze the aldol addition of DHAP to a variety of aldehydes and generate compounds with two stereocenters. This reaction is useful to synthesize chiral acyclic nucleosides, which constitute a well-known class of antiviral drugs currently used. In such compounds, the chirality of the aliphatic chain, which mimics the open pentose residue, is crucial for activity. In this work, three DHAP-dependent aldolases: fructose-1,6-biphosphate aldolase from rabbit muscle, rhanmulose-1-phosphate aldolase from

Indexed as

Aldehyde-LyasesEscherichia coliFructose-Bisphosphate AldolaseMolecular Docking SimulationPyrimidine NucleosidesThermotoga maritimaAnimalsDihydroxyacetone PhosphateRabbitsStereoisomerismAldehyde-LyasesDihydroxyacetone PhosphateFructose-Bisphosphate AldolaseL-fuculosephosphate aldolasePyrimidine Nucleosidesrhamnulose-1-phosphate adolasealdol reactionbiocatalysisdrug designstereoselectivity

Identifiers

PMID39062466
PMCPMC11274987

What OpenQuestion holds

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Registered trials

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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.