In one paragraphArticle in Marine drugs, 2026. 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 itWhat 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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
9 authors.
İbrahim S UrasFaculty of Pharmacy, Department of Pharmacognosy, Ağrı İbrahim Çeçen University, 04100 Ağrı, Turkey.ORCID 0000-0001-5945-8743 Pedro H S CandidoDepartment of Fundamental Chemistry, Institute of Chemistry, University of São Paulo, São Paulo 05508-000, SP, Brazil.
Catarina M LuísAssociate Laboratory i4HB, Institute for Health and Bioeconomy, NOVA School of Science and Technology, NOVA University of Lisbon, Campus Caparica, 2819-516 Caparica, Portugal.ORCID 0009-0006-0733-999X Vanda MarquesResearch Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisboa, Portugal.
Cecília M P RodriguesResearch Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003 Lisboa, Portugal.ORCID 0000-0002-4829-754X Rita G SobralAssociate Laboratory i4HB, Institute for Health and Bioeconomy, NOVA School of Science and Technology, NOVA University of Lisbon, Campus Caparica, 2819-516 Caparica, Portugal.ORCID 0000-0003-4533-7531 Anelize BaurmeisterDepartment of Fundamental Chemistry, Institute of Chemistry, University of São Paulo, São Paulo 05508-000, SP, Brazil.
Belma KonuklugilFaculty of Pharmacy, Department of Pharmacognosy, Lokman Hekim University, 06560 Ankara, Turkey.ORCID 0000-0002-4753-0450 Susana P GaudêncioAssociate Laboratory i4HB, Institute for Health and Bioeconomy, NOVA School of Science and Technology, NOVA University of Lisbon, Campus Caparica, 2819-516 Caparica, Portugal.ORCID 0000-0002-5510-1170 Funding
Applied Molecular Biosciences Unit LA/P/0140/2020Brazilian Federal Agency for Support and Evaluation of Graduate Education Finance Code 001Foundation for Science and Technology PTDC/MED-FAR/3492/2021Foundation for Science and Technology UID/04378/2025 and UID/PRR/04378/2025La Caixa Foundation LCF/PR/HR21/52410028National Council for Scientific and Technological Development 407675/2025-6São Paulo Research Foundation 2024/05211-4São Paulo Research Foundation 2025/24334-2the Turkish Antarctic Expeditions project TAE-II-6
6 · The paper itselfAbstract
Antarctic marine-derived fungi represent an underexplored reservoir of bioactive secondary metabolites shaped by extreme environmental pressures. In this study, nine fungal isolates obtained from Antarctic macroalgae, lichens, sponge tissue, and sediments were evaluated for their antimicrobial, anticancer, antibiofilm, and metabolomic profiles. Untargeted LC-MS/MS molecular networking (GNPS) revealed a chemically rich metabolome, dominated by alkaloids, followed by polyketides, meroterpenoids, and diketopiperazines, with
Indexed as
Anti-Bacterial AgentsAnti-Infective AgentsAquatic OrganismsBiofilmsFungiAnimalsAntarctic RegionsAntineoplastic AgentsAspergillusCladosporiumHCT116 CellsHumansMetabolomicsMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsTandem Mass SpectrometryAnti-Bacterial AgentsAnti-Infective AgentsAntineoplastic Agentsantibiofilm and cytotoxicity activitiesantimicrobialblue biotechnologyextreme environmentsGNPS molecular networkingmarine-derived Antarctic funginatural productssecondary metabolitesuntargeted LC–MS/MS
Identifiers
PMID42646467
PMCPMC13514757
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