Evidence map›Paper›PMID 42518337›Full record

ArticleBeilstein journal of organic chemistry2026

Synthesis of functionalized, 13-alkyl-substituted coralyne derivatives and investigation of their interactions with duplex and abasic site-containing DNA.

Laurin Beckmann, Jason Lennard Kunze, Hannah Karola Strunk, Maurice Michel, Heiko Ihmels

Abstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

5 authors.

Laurin BeckmannDepartment of Chemistry-Biology, and Research Center of Micro- and Nanochemistry and (Bio-)Technology (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57068 Siegen, Germany.
Jason Lennard KunzeDepartment of Chemistry-Biology, and Research Center of Micro- and Nanochemistry and (Bio-)Technology (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57068 Siegen, Germany.
Hannah Karola StrunkDepartment of Chemistry-Biology, and Research Center of Micro- and Nanochemistry and (Bio-)Technology (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57068 Siegen, Germany.ORCID https://orcid.org/0009-0008-4945-9409
Maurice MichelDepartment of Oncology and Pathology, Karolinska Institutet Science for Life Laboratory, Alpha 5, Tomtebodavägen 23a, 171 65 Solna, Sweden.ORCID https://orcid.org/0000-0003-3261-2493
Heiko IhmelsDepartment of Chemistry-Biology, and Research Center of Micro- and Nanochemistry and (Bio-)Technology (Cμ), University of Siegen, Adolf-Reichwein-Str. 2, 57068 Siegen, Germany.ORCID https://orcid.org/0000-0003-0969-0426

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the goal to develop coralyne-based ligands for abasic site-containing DNA (AP-DNA), different synthetic routes towards the functionalization of coralyne were tested. In particular, the alkylation of the benzylic position in papaverine and subsequent cyclization by treatment with acetic anhydride in sulfuric acid led to the synthesis of a coralyne derivative with an alkoxyamine-functionalized linker attached at position C13. Firstly, it was demonstrated with a resembling model compound that the alkylation of the coralyne scaffold does not influence the DNA-binding properties. Furthermore, it was shown that the alkoxyamine function can be readily released from a Boc-protected precursor and that the corresponding coralyne-alkoxyamine conjugate can operate as a ligand for AP-DNA and as inhibitor of enzymatic repair of abasic sites.

Indexed as

APE1 inhibitionDNA bindersN-hetarenespapaverineprotoberberines

Identifiers

PMID42518337
PMCPMC13382958

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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.