Evidence map›Paper›PMID 41252588›Full record

ArticleChemMedChem2026

Development and Characterization of a Noncovalent Stimulator of Interferon Genes Proteolysis-Targeting Chimeras.

Bo Hu, Adam S Duerfeldt

Abstract read
In one paragraph

Article in ChemMedChem, 2026. 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
–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

2 citing papers in PubMed.

  1. Therapeutic targeting of the cGAS-STING pathway in human disease.The Journal of clinical investigation · 2026
    Review
  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

2 authors.

Bo HuDepartment of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis, MN, 55455, USA.
Adam S DuerfeldtDepartment of Medicinal Chemistry, College of Pharmacy, University of Minnesota, Minneapolis, MN, 55455, USA.ORCID https://orcid.org/0000-0002-3130-9890

Funding

Bifunctional Inhibitors of STING as Chemical Probes for Diabetic RetinopathyR21EY035454 · NEI · UNIVERSITY OF MINNESOTA · PI DUERFELDT, ADAM SCOTT · 2024 to 2025
$418k
Foundation for the National Institutes of Health R21EY035454NEI NIH HHS R21 EY035454
6 · The paper itself

Abstract

The cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway activates the immune response upon detection of cytosolic dsDNA and is a key regulator of innate immunity. Overactivation of cGAS-STING has been implicated in numerous inflammatory diseases, and inhibition of cGAS-STING signaling has attracted significant interest as a therapeutic approach to attenuate aberrant inflammation. Proteolysis-targeting chimeras (PROTACs) have become popular modalities for catalyzing the degradation of proteins of interest, thus inhibiting their function. Herein, the design, synthesis, and characterization of noncovalent catalytic STING PROTACs based on a known diphenyl-dihydroisoquinolone STING inhibitory chemotype are reported. The lead from this series (BH690L) exhibits an effective concentration for half-maximal degradation (DC

Indexed as

InterferonsIsoquinolinesMembrane ProteinsAnimalsDose-Response Relationship, DrugHumansMolecular StructureProteolysisSTING ProteinStructure-Activity RelationshipInterferonsIsoquinolinesMembrane ProteinsSTING1 protein, humanSTING Proteincyclic GMP‐AMP synthaseinflammationprotein degradationproteolysis targeting chimerasstimulator of interferon genesstructure–activity relationships

Identifiers

PMID41252588
PMCPMC12811993

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.