Evidence mapPaperPMID 41847642Full record

ArticleACS medicinal chemistry letters2026

Targeting Protein Tyrosine Phosphatase 1B (PTP1B) to Improve Insulin Sensitivity Using Indole-Fused Glycyrrhetinic Acid Conjugates with Amino Acids.

Ledy De-la-Cruz-Martínez, David Equihua-González, Diana Laura Torres-Chacón, Erandi Ortiz-Barragán, J Martin Torres-Valencia, Rubria Marlen Martínez-Casares, Jaime Pérez-Villanueva, Martín González-Andrade, Julio César Almanza-Pérez, Francisco Cortés-Benítez

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2026. 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

10 authors.

Ledy De-la-Cruz-MartínezDoctorado en Ciencias Farmacéuticas, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana - Unidad Xochimilco, Ciudad de México 04960, Mexico.
David Equihua-GonzálezDepartamento de Sistemas Biológicos, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana - Unidad Xochimilco, Ciudad de México 04960, Mexico.
Diana Laura Torres-ChacónLaboratorio de Farmacología, Departamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud,Universidad Autónoma Metropolitana - Unidad Iztapalapa, Ciudad de México 09340, Mexico.
Erandi Ortiz-BarragánLaboratorio de Farmacología, Departamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud,Universidad Autónoma Metropolitana - Unidad Iztapalapa, Ciudad de México 09340, Mexico.
J Martin Torres-ValenciaÁrea Académica de Química, Universidad Autónoma del Estado de Hidalgo, Hidalgo 42184, Mexico.ORCID https://orcid.org/0000-0001-6426-7562
Rubria Marlen Martínez-CasaresDepartamento de Sistemas Biológicos, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana - Unidad Xochimilco, Ciudad de México 04960, Mexico.
Jaime Pérez-VillanuevaDepartamento de Sistemas Biológicos, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana - Unidad Xochimilco, Ciudad de México 04960, Mexico.
Martín González-AndradeLaboratorio de Biosensores y Modelaje Molecular, Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México 04510, Mexico.
Julio César Almanza-PérezLaboratorio de Farmacología, Departamento de Ciencias de la Salud, División de Ciencias Biológicas y de la Salud,Universidad Autónoma Metropolitana - Unidad Iztapalapa, Ciudad de México 09340, Mexico.ORCID https://orcid.org/0000-0002-9417-5500
Francisco Cortés-BenítezDepartamento de Sistemas Biológicos, División de Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana - Unidad Xochimilco, Ciudad de México 04960, Mexico.ORCID https://orcid.org/0000-0002-3954-8220

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein Tyrosine Phosphatase 1B (PTP1B) is a crucial enzyme that significantly modulates insulin and leptin signaling, making it a highly promising target for the treatment of type 2 diabetes (T2D). We previously reported the synthesis and inhibitory activity of FC-114, an indole-fused glycyrrhetinic acid derivative that potently inhibits PTP1B. In this study, we synthesized four FC-114 conjugates with amino acids at the C30 position to enhance their inhibitory activity against PTP1B

Indexed as

Amino acid conjugatesGLUT4 expressionGlycyrrhetinic acidProtein Tyrosine Phosphatase 1BType 2 diabetes

Identifiers

PMID41847642
PMCPMC12989875

What Socratic 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 Socratic graph.