Evidence map›Paper›PMID 39523872›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Crafting Molecular Tools for 15-Lipoxygenase-1 in a Single Step.

Anastasia Louka, Ntaniela Spacho, Dimitris Korovesis, Konstantinos Adamis, Christos Papadopoulos, Eirini-Eleni Kalaitzaki, Nektarios Tavernarakis, Constantinos G Neochoritis, Nikolaos Eleftheriadis

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Allosteric properties of mammalian ALOX15 orthologs.The Journal of biological chemistry · 2026
    Review
  3. The Evolution of Fluorescein into A Potential Theranostic Tool.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  4. Crafting Molecular Tools for 15-Lipoxygenase-1 in a Single Step.Angewandte Chemie (International ed. in English) · 2025
    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

9 authors.

Anastasia LoukaDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Ntaniela SpachoDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Dimitris KorovesisInstitute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Nikolaou Plastira 100, 70013, Heraklion, Greece.
Konstantinos AdamisDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Christos PapadopoulosDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Eirini-Eleni KalaitzakiDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Nektarios TavernarakisInstitute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, Nikolaou Plastira 100, 70013, Heraklion, Greece.
Constantinos G NeochoritisDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.
Nikolaos EleftheriadisDepartment of Chemistry, University of Crete, Voutes, 70013 Heraklion, Greece.ORCID https://orcid.org/0000-0002-1738-6419

Funding

Empeirikio FoundationGeneral Secretariat for Research and Technology TAEDR-0535850H2020 Marie Skłodowska-Curie Actions Grant agreement ID: 101130833Hellenic Foundation for Research and Innovation HFRI-FM17C3-0869, NeuroMitophagyHellenic Foundation for Research and Innovation Project Number: 0911Hellenic Foundation for Research and Innovation project number: 15511HORIZON EUROPE European Research Council ERC-GA695190-MANNA
6 · The paper itself

Abstract

Small molecule modulators are powerful tools for selectively probing and manipulating proteins in native biological systems. However, the development of versatile modulators that exhibit desired properties is hindered by the lack of a rapid and robust synthetic strategy. Here, we develop a facile and reliable one-step methodology for the generation of multifunctional toolboxes encompassing a wide variety of chemical modulators with different desired features. These modulators bind irreversibly to the protein target via a selective warhead. Key elements are introduced onto the warhead in a single step using multi-component reactions. To illustrate the power of this new technology, we synthesized a library of diverse modulators designed to explore a highly challenging and poorly understood protein, human 15-lipoxygenase-1. Modulators made include; activity-based/photoaffinity probes, chemosensors, photocrosslinkers, as well as light-controlled and high-affinity inhibitors. The efficacy of our compounds was successfully established through the provision of on demand inhibition and labeling of our target protein in vitro, in cellulo and in vivo; thus, proving that this technology has promising potential for applications in many complex biological systems.

Indexed as

Arachidonate 15-LipoxygenaseLipoxygenase InhibitorsSmall Molecule LibrariesAnimalsHumansMolecular StructureALOX15 protein, humanArachidonate 15-LipoxygenaseLipoxygenase InhibitorsSmall Molecule Librariescovalent inhibitorshuman 15-lipoxygenase-1photopharmacologyprobessmall molecule modulators

Identifiers

PMID39523872
PMCPMC11795718

What OpenQuestion holds

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LicenceCC BY-NC
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.