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Yukta Soni

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Review Aug 2026

Recent Developments in Triazolopyrimidine-based Cancer Therapeutics: A Mini Review.

The triazolopyrimidine ring has emerged as a ubiquitous and highly versatile structural motif found in a wide array of biologically active compounds. Owing to its unique fused heterocyclic architecture, this core is capable of engaging in diverse intermolecular interactions with biological targets. Such features have placed triazolopyrimidines as a particularly attractive scaffold in contemporary anticancer drug discovery. Over the past decade, and more conspicuously in the last five years, this framework has gained substantial attention due to its ability to modulate multiple cancer-relevant pathways with notable potency and selectivity. Strategic structural modifications, such as derivatization with appropriate substituents, hybridization with other pharmacophores, and metal complexation, have significantly enhanced their pharmacological profiles. These rational approaches not only improve efficacy and selectivity but also address key challenges, such as drug resistance, bioavailability, and off-target toxicity. Recent advances have also highlighted the potential of both organic derivatives and inorganic triazolopyrimidine-based complexes, particularly in the context of metallodrugs, where coordination with transition metals has led to improved cytotoxicity and novel mechanisms of action. Collectively, these developments highlight the promise of triazolopyrimidine scaffolds in transforming the current landscape of cancer therapy. This review critically summarizes and discusses the progress made in the design, synthesis, and anticancer evaluation of triazolopyrimidine-based organic and inorganic scaffolds reported in the scientific literature over the past five years, with an emphasis on their mechanisms of action and future therapeutic prospects.

I. Lumb, Jaskirat Singh, Yukta Soni et al. · 0 citations
Open access Jul 2026

4-Aminoquinoline derivatives and benzoxaborole-4-aminoquinoline hybrids: synthesis, antiplasmodial evaluation, heme-inhibition and in silico studies

A library of 4-aminoquinoline derivatives and benzoxaborole-4-aminoquinoline hybrids, linked through amide and 1H-1,2,3-triazole spacers, was synthesized and evaluated against both chloroquine-sensitive (3D7) and -resistant (W2) strains of Plasmodium falciparum. Structure–activity relationship studies revealed that antiplasmodial potency was strongly influenced by the length of the alkyl chain and by the nature of the terminal functional group (azido, aldehyde, or benzyl alcohol). Notably, incorporation of the benzoxaborole core significantly enhanced activity relative to the parent 4-aminoquinoline derivatives. Among the series, hybrid 8b emerged as the most potent analogue, displaying superior activity against the CQ-resistant W2 strain compared with the reference antimalarials quinine and chloroquine. The hybrids exhibited negligible cytotoxicity toward HEK-293 cells, affording selectivity indices of up to ∼700. UV-visible spectroscopic titrations demonstrated that compound 8b binds monomeric heme more selectively than CQ at both physiological and digestive vacuole pH, supporting inhibition of hemozoin formation as its primary mode of action. Furthermore, homology modelling, induced-fit docking, and molecular dynamics simulations with both wild-type and benzoxaborole-resistant (H36Y/D470N) PfCPSF3 suggested that the scaffold can maintain a stable Zn2+-coordinated binding mode in both protein variants. These findings indicate a potential dual mechanism involving hemozoin inhibition and PfCPSF3 targeting, warranting further experimental validation.

Anuradha Saini, Sumit Kumar, B. Pradines et al. · 0 citations

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