Evidence mapPaperPMID 32879651Full record

ArticleOxidative medicine and cellular longevity2020

Identification of New Targets and the Virtual Screening of Lignans against Alzheimer's Disease.

Mayara Dos Santos Maia, Gabriela Cristina Soares Rodrigues, Natália Ferreira de Sousa, Marcus Tullius Scotti, Luciana Scotti, Francisco Jaime B Mendonça-Junior

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Furofuranoid-Type Lignans and Related Phenolics fromPlants (Basel, Switzerland) · 2024
    Article
  4. Selene-Ethylenelacticamides andPathogens (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Nutrients · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. 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

6 authors at 2 institutions in 1 country.

Mayara Dos Santos MaiaLaboratory of Cheminformatics, Program of Natural and Synthetic Bioactive Products (PgPNSB), Health Sciences Center, Federal University of Paraíba, João Pessoa, PB, Brazil.
Gabriela Cristina Soares RodriguesLaboratory of Cheminformatics, Program of Natural and Synthetic Bioactive Products (PgPNSB), Health Sciences Center, Federal University of Paraíba, João Pessoa, PB, Brazil.
Natália Ferreira de SousaLaboratory of Cheminformatics, Program of Natural and Synthetic Bioactive Products (PgPNSB), Health Sciences Center, Federal University of Paraíba, João Pessoa, PB, Brazil.
Marcus Tullius ScottiLaboratory of Cheminformatics, Program of Natural and Synthetic Bioactive Products (PgPNSB), Health Sciences Center, Federal University of Paraíba, João Pessoa, PB, Brazil.ORCID https://orcid.org/0000-0003-4863-8057
Luciana ScottiLaboratory of Cheminformatics, Program of Natural and Synthetic Bioactive Products (PgPNSB), Health Sciences Center, Federal University of Paraíba, João Pessoa, PB, Brazil.ORCID https://orcid.org/0000-0003-1866-4107
Francisco Jaime B Mendonça-JuniorLaboratory of Synthesis and Drug Delivery, State University of Paraíba, João Pessoa, PB, Brazil.ORCID https://orcid.org/0000-0003-3588-833X
Universidade Federal da Paraíba · BRUniversidade Estadual da Paraíba · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is characterized by the progressive disturbance in cognition and affects approximately 36 million people, worldwide. However, the drugs used to treat this disease are only moderately effective and do not alter the course of the neurodegenerative process. This is because the pathogenesis of AD is mainly associated with oxidative stress, and current drugs only target two enzymes involved in neurotransmission. Therefore, the present study sought to identify potential multitarget compounds for enzymes that are directly or indirectly involved in the oxidative pathway, with minimal side effects, for AD treatment. A set of 159 lignans were submitted to studies of QSAR and molecular docking. A combined analysis was performed, based on ligand and structure, followed by the prediction of absorption, distribution, metabolism, excretion, and toxicity (ADMET) properties. The results showed that the combined analysis was able to select 139 potentially active and multitarget lignans targeting two or more enzymes, among them are c-Jun N-terminal kinase 3 (JNK-3), protein tyrosine phosphatase 1B (PTP1B), nicotinamide adenine dinucleotide phosphate oxidase 1 (NOX1), NADPH quinone oxidoreductase 1 (NQO1), phosphodiesterase 5 (PDE5), nuclear factor erythroid 2-related factor 2 (Nrf2), cycloxygenase 2 (COX-2), and inducible nitric oxide synthase (

Indexed as

Drug Evaluation, PreclinicalUser-Computer InterfaceAlgorithmsAlzheimer DiseaseCyclic Nucleotide Phosphodiesterases, Type 5Databases, ChemicalHumansHydrogen BondingLignansMolecular Docking SimulationProtein Tyrosine Phosphatase, Non-Receptor Type 1Quantitative Structure-Activity RelationshipROC CurveThermodynamicsCyclic Nucleotide Phosphodiesterases, Type 5LignansProtein Tyrosine Phosphatase, Non-Receptor Type 1

Identifiers

PMID32879651
PMCPMC7448245
OpenAlexW3049343770

What Socratic 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 Socratic graph.