Evidence map›Paper›PMID 42224357›Full record

ArticlePloS one2026

Dimercaprol (BAL): Insights into conformational stability, fragmentation pathways via tandem LR-ESI, HR-EI mass spectrometry, and gas-phase thermochemical properties from quantum chemical calculations.

Miguel Fernando Molano, Alba Marcela Gómez Gómez, Alejandro Moncayo-Lasso, Carlos A Bejarano, John Edward Diaz, Cristian Buendía-Atencio, Miguel Ángel Delgado, Vaneza Paola Lorett Velásquez, Alix E Loaiza, Sol M Mejía

Abstract read
In one paragraph

Article in PloS one, 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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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Miguel Fernando MolanoDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
Alba Marcela Gómez GómezDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
Alejandro Moncayo-LassoDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
Carlos A BejaranoDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
John Edward DiazDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.
Cristian Buendía-AtencioDepartamento de Química, Facultad de Ciencias, Universidad Antonio Nariño, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-6375-3382
Miguel Ángel DelgadoFacultad de Ciencias y Educación, Universidad Distrital Francisco José de Caldas, Bogotá, Colombia.ORCID https://orcid.org/0000-0002-5832-5831
Vaneza Paola Lorett VelásquezFacultad de Medicina y Ciencias de la Salud, Grupo de Investigación sobre Agentes Radiológicos, Biológicos y Químicos, Universidad Militar Nueva Granada, Bogotá, Colombia.
Alix E LoaizaDepartamento de Química, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.
Sol M MejíaDepartamento de Química, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.ORCID https://orcid.org/0000-0001-5664-0558

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dimercaprol (British antilewisite, BAL) is a long-established chelating agent used in the treatment of heavy metal poisoning; however, its physicochemical and thermochemical properties have not yet been fully characterized. In this study, we combined gas-phase quantum chemical calculations with high-resolution mass spectrometry to investigate the conformational stability, fragmentation pathways, and thermochemical parameters of BAL. Fragmentation behavior was examined by gas chromatography/mass spectrometry-QTOF under electronic ionization conditions, and the resulting spectra were interpreted through proposed dissociation pathways involving water, hydrogen sulfide, and thiyl radical losses, supported by reaction enthalpies calculated at the theoretical level M06-2X/6-311++G(3df,3pd). Conformational analysis identified five low-energy structures (BAL-1 to BAL-5), where intramolecular hydrogen bonds and gauche/anti interactions play a key role in stability; BAL-3 was consistently predicted as the lowest-energy conformer. Vibrational frequencies calculated with the B3LYP, M06-2X, and MN15 functionals showed good agreement with experimental FTIR and Raman data. The thermochemical properties were further evaluated using Gn composite methods (G3MP2B3, G3B3, G4MP2 and G4) which yielded an average standard enthalpy of formation at ΔH°(f,298K) of -45.6 ± 1.1 kcal/mol. This work provides a detailed experimental and theoretical characterization of dimercaprol, providing information on its possible fragmentation mechanism and conformational landscape, and offering a thermochemical framework that could support future pharmacological, toxicological and environmental applications.

Indexed as

Chelating AgentsGas Chromatography-Mass SpectrometryGasesHydrogen BondingModels, MolecularMolecular ConformationQuantum TheorySpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryThermodynamicsChelating AgentsGases

Identifiers

PMID42224357
PMCPMC13225642

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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.