ArticleChemistry & biodiversity2026
Synthesis, Anticancer Evaluation, and Molecular Docking of Triazolylmethyl-Dihydroquinazolinyl Benzoate Derivatives as Potential PARP-1 Inhibitors.
Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Exploring the Anticancer Potential of Novel Piperidine-Embedded Isoxazol-Triazole Conjugates Against MCF-7 Human Breast Adenocarcinoma Cell Line: Design, Synthesis, In Silico, and In Vitro Investigations.Chemistry & biodiversity · 2026Article
- PEGylated Heterofunctional Dendrimers Enable Multivalent Diclofenac Delivery for ROS-Driven Anticancer Activity.ACS applied materials & interfaces · 2026Article
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Authors and funding
8 authors.
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Abstract
Quinazolinone derivatives have emerged as promising scaffolds in medicinal chemistry due to their broad spectrum of biological activities, including anticancer potential. Incorporation of triazole rings through click chemistry has further boosted the pharmacological relevance of such compounds, due to the triazole's stability, bioisosterism, and ability to engage in key interactions with biological targets. Motivated by these properties, a library of 24 triazolylmethyl-dihydroquinazolinyl benzoate (TDB) derivatives (7a-x) was synthesized using a click chemistry strategy, starting from anthranilamide and phthalic anhydride. The structures of the synthesized compounds were established through IR,
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