Evidence map›Paper›PMID 40454050›Full record

ArticleACS omega2025

Crystal Structure of Melphalan Hydrochloride and Its Association with Caffeine Improves Its Antineoplastic Action.

Juliana Pereira da Silva, Carin Cristina da Silva Batista, Maria Lúcia Schumacher, Santiago Rodriguez, Alan Talevi, Paula Haddad, Guillermo Raul Castro, Fabio Furlan Ferreira

Abstract read
In one paragraph

Article in ACS omega, 2025. 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

8 authors.

Juliana Pereira da SilvaCentro de Ciências Naturais e Humanas (CCNH), Universidade Federal Do ABC (UFABC), Av. Dos Estados, 5001, Santo André, São Paulo 09280-560, Brazil.
Carin Cristina da Silva BatistaCentro de Ciências Naturais e Humanas (CCNH), Universidade Federal Do ABC (UFABC), Av. Dos Estados, 5001, Santo André, São Paulo 09280-560, Brazil.
Maria Lúcia SchumacherInstituto de Ciências Ambientais, Químicas e Farmacêuticas, Departamento de Química, Universidade Federal de São Paulo, Rua São Nicolau, 210, Diadema, São Paulo 09913-030, Brazil.
Santiago RodriguezLaboratorio de Investigación y Desarrollo de Bioactivos (LIDeB), Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata (UNLP), Calle 47 y 115 (B1900AD), La Plata, Buenos Aires B1001, Argentina.
Alan TaleviLaboratorio de Investigación y Desarrollo de Bioactivos (LIDeB), Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata (UNLP), Calle 47 y 115 (B1900AD), La Plata, Buenos Aires B1001, Argentina.ORCID https://orcid.org/0000-0003-3178-826X
Paula HaddadInstituto de Ciências Ambientais, Químicas e Farmacêuticas, Departamento de Química, Universidade Federal de São Paulo, Rua São Nicolau, 210, Diadema, São Paulo 09913-030, Brazil.ORCID https://orcid.org/0000-0001-5362-1861
Guillermo Raul CastroCentro de Ciências Naturais e Humanas (CCNH), Universidade Federal Do ABC (UFABC), Av. Dos Estados, 5001, Santo André, São Paulo 09280-560, Brazil.ORCID https://orcid.org/0000-0002-6187-7805
Fabio Furlan FerreiraCentro de Ciências Naturais e Humanas (CCNH), Universidade Federal Do ABC (UFABC), Av. Dos Estados, 5001, Santo André, São Paulo 09280-560, Brazil.ORCID https://orcid.org/0000-0003-1516-1221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melphalan hydrochloride (MEH) is a chemotherapy drug with antitumor activity, recognized for its classification as an alkylating agent. Over the past few decades, the drug has been administered to patients undergoing treatment for breast and ovarian cancers, and it is also intended for the treatment of multiple myeloma. It is commercially available in tablet and injection forms; however, its oral administration presents some limitations, including presystemic elimination and incomplete absorption. This study employs a simulated annealing approach and powder X-ray diffraction data to determine its crystal structure. The structure is confirmed by Rietveld refinement, which reveals good visual agreement between the generated model and experimental data. Given that MEH has low solubility in water, a screening conducted in the Mercury program (utilizing the CSD-Materials module) indicates the potential use of various molecular synthons to enhance the drug's efficacy. Grinding processes (manual and mechanochemical) are conducted with MEH and a coformer, caffeine (CAF), to form stoichiometric mixtures. The vibrational characteristics associated with MEH and CAF show low energy levels. The effects on cell viability of the MEH-CAF combination are studied at different concentrations and reveal more significant cytotoxicity against the HeLa cell line (cervical tumor) compared to healthy MRC-5 cells (human fetal lung fibroblasts).

Identifiers

PMID40454050
PMCPMC12120582

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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.