Evidence map›Paper›PMID 29376367›Full record

ArticleJournal of the American Chemical Society2018

Potent and Selective Inhibitors of 8-Oxoguanine DNA Glycosylase.

Yu-Ki Tahara, Douglas Auld, Debin Ji, Andrew A Beharry, Anna M Kietrys, David L Wilson, Marta Jimenez, Daniel King, Zachary Nguyen, Eric T Kool

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

57 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Article
  3. CypD Dependent mPTP Opening Is Crucial for Oxidized Mitochondrial DNA Release in Ferroptosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. 8-Oxoguanine: A Lesion, an Epigenetic Mark, or a Molecular Signal?International journal of molecular sciences · 2025
    Review
  5. Review
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  19. Review
  20. There's more to enzyme antagonism than inhibition.Bioorganic & medicinal chemistry · 2023
    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.

Yu-Ki TaharaDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.
Douglas AuldDepartment of Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research , 250 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Debin JiDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.
Andrew A BeharryDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.
Anna M KietrysDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.
David L WilsonDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.ORCID 0000-0002-1922-427X
Marta JimenezDepartment of Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research , 250 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Daniel KingDepartment of Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research , 250 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Zachary NguyenDepartment of Chemical Biology and Therapeutics, Novartis Institutes for Biomedical Research , 250 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Eric T KoolDepartment of Chemistry, Stanford University , Stanford, California 94305, United States.ORCID 0000-0002-7310-2935
Stanford University · US

Funding

Measuring and Modulating Oxidative DNA Damage Surveillance PathwaysR01CA217809 · NCI · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2017 to 2024
$3.7M
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLDR01GM067201 · NIGMS · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2003 to 2011
$2.2M
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular ContextsR01GM110050 · NIGMS · STANFORD UNIVERSITY · PI KOOL, ERIC T. · 2015 to 2018
$1.2M
NCI NIH HHS R01 CA217809NIGMS NIH HHS R01 GM067201NIGMS NIH HHS R01 GM110050
6 · The paper itself

Abstract

The activity of DNA repair enzyme 8-oxoguanine DNA glycosylase (OGG1), which excises oxidized base 8-oxoguanine (8-OG) from DNA, is closely linked to mutagenesis, genotoxicity, cancer, and inflammation. To test the roles of OGG1-mediated repair in these pathways, we have undertaken the development of noncovalent small-molecule inhibitors of the enzyme. Screening of a PubChem-annotated library using a recently developed fluorogenic 8-OG excision assay resulted in multiple validated hit structures, including selected lead hit tetrahydroquinoline 1 (IC

Indexed as

Antineoplastic AgentsCaco-2 CellsDNA GlycosylasesEnzyme InhibitorsGuanineHEK293 CellsHeLa CellsHumansNeoplasmsSmall Molecule Libraries8-hydroxyguanineAntineoplastic AgentsDNA GlycosylasesEnzyme InhibitorsGuanineoxoguanine glycosylase 1, humanSmall Molecule Libraries

Identifiers

PMID29376367
PMCPMC5823510
OpenAlexW2785310437

What OpenQuestion holds

Textmetadata
LicenceTDM
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.