Evidence map›Paper›PMID 42337968›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026

Fluorogenic Sydnones for Bioorthogonal Labeling of DNA.

Kerstin Müller, Hans-Achim Wagenknecht

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kerstin MüllerInstitut of Organic Chemistry, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.
Hans-Achim WagenknechtInstitut of Organic Chemistry, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.ORCID https://orcid.org/0000-0003-4849-2887

Funding

Deutsche Forschungsgemeinschaft Wa 1386/22-1 and 22-2KIT
6 · The paper itself

Abstract

Five cyanine-styryl dyes were synthetically conjugated to sydnones combining fluorogenicity with bioorthogonal reactivity. The synthesis was based on synthetic modules and building blocks using Heck couplings as central conjugation steps. The novel cyanine-styryl dyes show significant Stokes shifts to well separate excitation and emission for fluorescent cell imaging. Reaction kinetics and fluorogenicity of the strain-promoted sydnone-alkyne cycloaddition (SPSAC) with 7-deazadenosine, 7-deaza-2'-deoxyadenosine and DNA modified by bicyclo[6.1.0]non-4-yne (BCN) were investigated by spectroscopic means. The determined second-order rate constants k

Indexed as

CarbocyaninesDNAFluorescent DyesAlkynesCycloaddition ReactionDeoxyadenosinesFluorescent Chemosensor CompoundsHeLa CellsHumansKineticsTubercidinAlkynesCarbocyaninesDeoxyadenosinesDNAFluorescent Chemosensor CompoundsFluorescent DyesTubercidincyanine dyeDNAfluorescenceRNAsynthesis

Identifiers

PMID42337968
PMCPMC13628573

What OpenQuestion holds

Textmetadata
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.