Evidence map›Paper›PMID 41420346›Full record

ReviewAngewandte Chemie (International ed. in English)2026

Diazirines Beyond Photoaffinity Labeling: A Comprehensive Overview of Applications in Biological Sciences, Materials Chemistry, and NMR-Spectroscopy.

Dominik Schnalzer, Viktor Savic, Clemens Cziegler, Michael Schnürch, Marko D Mihovilovic

Abstract readReview
In one paragraph

Review in Angewandte Chemie (International ed. in English), 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. 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

5 authors.

Dominik Schnalzer *Institute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163, Vienna, 1060, Austria.ORCID 0009-0003-0469-197X
Viktor Savic *Institute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163, Vienna, 1060, Austria.ORCID 0000-0002-0018-2882
Clemens CzieglerInstitute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163, Vienna, 1060, Austria.ORCID 0009-0005-3721-1922
Michael SchnürchInstitute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163, Vienna, 1060, Austria.ORCID 0000-0003-2946-9294
Marko D MihovilovicInstitute of Applied Synthetic Chemistry, TU Wien, Getreidemarkt 9/163, Vienna, 1060, Austria.ORCID 0000-0002-5438-8368

Funding

Austrian Science Fund TAI6911924
6 · The paper itself

Abstract

Diazirines are well-known for their role in photoaffinity labeling (PAL) probes, acting as reactive groups to fish out proteins for drug target identification or tag installation. Their key asset lies in the precise activation through UV light, heat, or voltage, and in the ability to covalently bind to organic materials. However, the versatility of diazirines extends beyond this application. It was demonstrated that diazirines act as diverse entities, functioning as bridging units to connect different materials or reinforce polymers for applications such as bulletproof armor. Some facilitate blending of non-mixable polymers, allowing the disassembly for recycling. Others serve as glues, aiding wound healing, or immobilize molecules on surfaces, creating new material and surface properties. Some contribute to the fabrication of elastic electronic materials, and others function as magnetic resonance imaging (MRI) biolabels without the need for a "conventional hook function." This review intends to showcase diazirines beyond PAL and provide an overview of these applications, often combined across different fields. In this regard, the chemistry of diazirines demonstrates how different disciplines draw inspiration from one another, disclosing exciting new methodologies. This review intends to inspire the development of further innovative methods and applications.

Indexed as

DiazomethanePhotoaffinity LabelsHumansMagnetic Resonance SpectroscopyDiazomethanePhotoaffinity LabelsBioadhesivesCarbene sourcesDiazirinesMaterials sciencePolymer crosslinking

Identifiers

PMID41420346
PMCPMC12828484

What OpenQuestion holds

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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 OpenQuestion graph.