ArticleJournal of fluorescence2025
New Fluorescent Synthetic Retinoids as Potential RAR Agonists with Anticancer, Molecular Docking and ADME Assessments.
Article in Journal of fluorescence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
4 authors.
Funding
Abstract
Natural and synthetic retinoids are derivatives of vitamin A that mediate different transcriptional activities. Synthesis of fluorescent probes can be a useful tool in cellular imaging and understanding different regulatory signaling pathways. In this study, new fluorescent synthetic retinoid analogues (3a, 3b, 4a, and 4b) were prepared and biologically screened against six different cancer and normal cell lines for assessment of their anticancer and fluorescent activities. A combination of biological assays, such as MTT, flow cytometry, gene and protein expression analysis, DNA fragmentation, and ATPase activity assays, as well as in-silico and ADME studies, was performed. All new compounds showed anti-proliferative activity (2.09-132.70 µM) against different cancer cell types with minimal cytotoxicity (SI > 1), and the Caco-2 cancer cell line was selected for further in vitro investigation. All compounds showed cell cycle arrest at the SubG
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Registered trials
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