Evidence map›Paper›PMID 42872199›Full record

ArticleRSC medicinal chemistry2026

Dimercaptosuccinic acid (DMSA) mono-esters and amides: synthesis and application in treating metal induced drug resistance in lung cancer.

Carissa M Lloyd, Hannah L Richards, Katherine E V Deck, Toby Blundell, Natalie Pridmore, Michael Stalhamer, Dan Gelvan, Patricia A J Muller, William D G Brittain

Abstract read
In one paragraph

Article in RSC medicinal 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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0citing papers in PubMed
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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

9 authors.

Carissa M LloydDepartment of Chemistry, Durham University South Road Durham DH1 3LE UK william.d.brittain@durham.ac.uk.ORCID https://orcid.org/0000-0001-5229-3675
Hannah L RichardsDepartment of Biosciences, Durham University Durham DH1 3LE UK patricia.muller@durham.ac.uk.ORCID https://orcid.org/0009-0008-5687-0976
Katherine E V DeckDepartment of Chemistry, Durham University South Road Durham DH1 3LE UK william.d.brittain@durham.ac.uk.ORCID https://orcid.org/0009-0007-6135-0353
Toby BlundellDepartment of Chemistry, Durham University South Road Durham DH1 3LE UK william.d.brittain@durham.ac.uk.ORCID https://orcid.org/0000-0002-7296-1471
Natalie PridmoreDepartment of Chemistry, Durham University South Road Durham DH1 3LE UK william.d.brittain@durham.ac.uk.
Michael StalhamerPleco Therapeutics BV Roggestraat 111 7311 CC Apeldoorn The Netherlands.
Dan GelvanPleco Therapeutics USA 3900 E. Valley Ct Raleigh NC 27606 USA.ORCID https://orcid.org/0009-0008-4769-8051
Patricia A J MullerDepartment of Biosciences, Durham University Durham DH1 3LE UK patricia.muller@durham.ac.uk.ORCID https://orcid.org/0000-0002-0926-1499
William D G BrittainDepartment of Chemistry, Durham University South Road Durham DH1 3LE UK william.d.brittain@durham.ac.uk.ORCID https://orcid.org/0000-0002-2876-5895

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dimercaptosuccinic acid (DMSA) mono-esters have been shown to be powerful chelators that are capable of heavy metal removal across a variety of biological applications. Whilst the utility of this class of chelator is widely reported in acute heavy metal poisoning the ability to access a wide variety of derivatives has been a synthetic challenge often relying on the use of statistical mixtures governed by stoichiometry. In this report we detail a robust four-step synthetic route starting from commercially available acetylenedicarboxylic acid that can generate both dimercaptosuccinic acid mono-esters and mono-amides. These compounds were tested for their ability to resensitize transition metal-induced chemotherapy resistance in lung cancer cells. Similarly to previous studies focused on a single dimercaptosuccinic ester (MiADMSA) many of the analogues generated were able to cause resensitisation toward doxorubicin significantly decreasing its IC

Identifiers

PMID42872199
PMCPMC13660734

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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.