Evidence map›Paper›PMID 42047753›Full record

ArticleJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry2026

Ag(I) complexes with natural products and triphenylphosphine: activity against tumor cell lines and mycobacterium tuberculosis.

Jocely Lucena Dutra, João Honorato de Araujo-Neto, Rafael Wendel Rodrigues Santana, Rone Aparecido De Grandis, Giulia Polinário, Fernando Rogério Pavan, Javier Ellena, Alzir Azevedo Batista

Abstract read
In one paragraph

Article in Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic 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
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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

8 authors.

Jocely Lucena DutraDepartament of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, SP, CEP 13561-905, Brazil. jocely.dut@hotmail.com.
João Honorato de Araujo-NetoDepartment of Fundamental Chemistry, Institute of Chemistry, University of São Paulo (USP), São Paulo, SP, CEP 05508-000, Brazil.
Rafael Wendel Rodrigues SantanaDepartament of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, SP, CEP 13561-905, Brazil.
Rone Aparecido De GrandisDepartment of Biological Sciences, School of Pharmaceutical Sciences of São Paulo State University (UNESP), Araraquara, SP, CEP 14800-903, Brazil.
Giulia PolinárioDepartment of Biological Sciences, School of Pharmaceutical Sciences of São Paulo State University (UNESP), Araraquara, SP, CEP 14800-903, Brazil.
Fernando Rogério PavanDepartment of Biological Sciences, School of Pharmaceutical Sciences of São Paulo State University (UNESP), Araraquara, SP, CEP 14800-903, Brazil.
Javier EllenaSão Carlos Institute of Physics, University of São Paulo (USP), CP 369, São Carlos, SP, CEP 13560-970, Brazil.
Alzir Azevedo BatistaDepartament of Chemistry, Federal University of São Carlos (UFSCar), São Carlos, SP, CEP 13561-905, Brazil. daab@ufscar.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer and tuberculosis remain among the leading causes of morbidity and mortality worldwide, and the emergence of drug resistance in both diseases highlights the urgent need for new therapeutic strategies. In this context, metal-based compounds combined with bioactive natural products have emerged as promising alternatives to conventional drugs. In the present study, a series of silver (I) complexes containing natural products (curcumin, lawsone, lapachol or alizarin) and triphenylphosphine (PPh3) (complexes 1–4) were synthesized and structurally characterized by IR spectroscopy, elemental analysis, molar conductivity, NMR (1H, 13C, 31P{1H}) spectroscopy and single crystal X-ray diffraction. The results of single crystal diffraction show that the two silver complexes are four-coordinated with two PPh3 and two O atoms of natural product, forming a distorted tetrahedral geometry. The in vitro cytotoxicity of silver(I) complexes was evaluated by MTT assay against four cancer cells and two normal cells, the result shows that the complexes presented a low IC50 value in general, including in normal cell lines. The complexes show better cytotoxic activity for A2780cis (cisplatin-resistant ovarian tumor cell line), being nearly 30 times higher than cisplatin. Silver complexes were tested against Mycobacterium tuberculosis (Mtb) reaching the threshold for effective antimicrobial activity. Furthermore, complex 4 showed good activity against clinical isolates of Mtb resistant to multiple first-line anti-TB drugs.

Indexed as

Antineoplastic AgentsAntitubercular AgentsBiological ProductsCoordination ComplexesMycobacterium tuberculosisOrganophosphorus CompoundsSilverCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorHumansMicrobial Sensitivity TestsMolecular StructureAntineoplastic AgentsAntitubercular AgentsBiological ProductsCoordination ComplexesOrganophosphorus CompoundsSilvertriphenylphosphineAnti-mycobacterium tuberculosisCytotoxicityNatural productsSilver(I) complexes

Identifiers

PMID42047753
PMCPMC13287109

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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.