Evidence map›Paper›PMID 41428972›Full record

ArticleBlood advances2026

Small-molecule inhibition of γ-glutamyl carboxylase reveals a novel anticoagulant strategy.

Guomin Shen, Dan Song, Shixin Li, Xuejie Chen, Catherine E Richter, Shixia Dong, Yiming Guo, Hongli Liu, Yan Shen, Zhenyu Hao and 4 more

Abstract read
In one paragraph

Article in Blood advances, 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. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Guomin ShenDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.ORCID 0000-0002-5006-2790
Dan SongDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.ORCID 0009-0000-6143-8995
Shixin LiDepartment of Bioengineering, College of Bioscience and Biotechnology, Yangzhou University, Yangzhou, People's Republic of China.ORCID 0000-0001-8297-0972
Xuejie ChenDepartment of Biology, The University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0001-8459-2557
Catherine E RichterDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI.ORCID 0000-0001-9377-5267
Shixia DongDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.ORCID 0000-0001-5583-2048
Yiming GuoDepartment of Hematology, The Second Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.ORCID 0009-0008-4572-7111
Hongli LiuSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, People's Republic of China.ORCID 0000-0001-9638-0578
Yan ShenHenan International Joint Laboratory of Thrombosis and Hemostasis, College of Medicine, Henan University of Science and Technology, Luoyang, People's Republic of China.
Zhenyu HaoDepartment of Bioengineering, College of Bioscience and Biotechnology, Yangzhou University, Yangzhou, People's Republic of China.ORCID 0000-0001-6418-2921
Darrel W StaffordDepartment of Biology, The University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0001-6830-3874
Jordan A ShavitDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI.ORCID 0000-0002-2874-4904
Qing CaoState Key Laboratory of Reproductive Medicine and Offspring Health, Nanjing Medical University, Nanjing, People's Republic of China.ORCID 0000-0003-2517-2231
Jian-Ke TieDepartment of Biology, The University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-8447-3408

Funding

Genetic and therapeutic studies of hemostatic and thrombotic disorders using zebrafishR35HL150784 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jordan A. Shavit · 2020 to 2026
$5.4M
Characterization of enzymes in the vitamin K cycleR01HL131690 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI STAFFORD, DARREL W, TIE, JIANKE · 2016 to 2023
$4.0M
NHLBI NIH HHS R01 HL131690NHLBI NIH HHS R35 HL150784
6 · The paper itself

Abstract

abstractOral anticoagulants such as warfarin, which function as vitamin K antagonists (VKAs), have long been central to anticoagulation therapy. Warfarin inhibits vitamin K epoxide reductase (VKOR), thereby restricting the availability of reduced vitamin K and impairing γ-carboxylation and activation of vitamin K-dependent clotting factors (VKDCFs). However, warfarin's clinical use is hindered by a narrow therapeutic index and marked interindividual variability, largely attributable to genetic variation in VKOR, yet it remains the only oral anticoagulant option for clinical conditions such as antiphospholipid antibody syndrome. γ-Glutamyl carboxylase (GGCX), the enzyme that directly modifies VKDCFs, represents an attractive but largely unexplored target for anticoagulation. Using a cell-based high-throughput screen of the Maybridge Hit-Finder compound library (comprising 14 400 drug-like molecules), we identified 21 compounds that inhibited γ-carboxylation of VKDCFs. Subsequent gene-deficient cell-based assays and in vitro enzymatic characterization revealed that compound HF13141-H5 selectively and potently inhibits GGCX activity, with nanomolar half-maximal inhibitory concentrations. Molecular docking with the recently resolved GGCX structure suggested that HF13141-H5 mimics the binding of reduced vitamin K, and site-directed mutagenesis confirmed the critical hydrogen bond with residue N290 within the substrate-binding pocket. Importantly, HF13141-H5 maintained full inhibitory potency against VKOR variants associated with warfarin resistance and demonstrated robust anticoagulant activity in a zebrafish laser-induced endothelial injury model. In summary, we describe the discovery and mechanistic characterization of HF13141-H5 as the first small-molecule GGCX inhibitor. By directly targeting GGCX, HF13141-H5 presents a promising strategy for developing next-generation anticoagulants that could overcome the limitations of warfarin, such as genetic variability and resistance.

Indexed as

AnticoagulantsCarbon-Carbon LigasesEnzyme InhibitorsSmall Molecule LibrariesAnimalsHumansMolecular Docking SimulationVitamin K Epoxide ReductasesZebrafishAnticoagulantsCarbon-Carbon LigasesEnzyme Inhibitorsglutamyl carboxylaseSmall Molecule LibrariesVitamin K Epoxide Reductases

Identifiers

PMID41428972
PMCPMC13068808

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.