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February 6, 2026RSC Advances2 citationsOpen Access

Novel pyridine-heterocycle hybrids: synthesis via Hantzsch and Biginelli reactions, docking simulations, and anticancer activity

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HDHadeer M. DiabMSMostafa E. SalemAEAhmed H. M. Elwahy

Key Points

  • The aim is to synthesize novel pyridine-heterocycle hybrids and evaluate their anticancer activity.
  • Synthesis of hybrids using Hantzsch and Biginelli reactions.
  • Evaluation of anticancer activity through experimental methods.
  • Docking simulations to assess structure–activity relationships.
  • Novel hybrids exhibit promising anticancer activity.
  • Docking simulations provide insights into effective interactions with cancer-related targets.

Abstract

Novel pyridine–heterocycle hybrids were synthesized via Hantzsch and Biginelli reactions. Anticancer activity was evaluated experimentally and supported by docking studies, providing insight into structure–activity relationships.

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Cite This Study

Diab et al. (2026) studied this question.

synapsesocial.com/papers/698585678f7c464f23008c5chttps://doi.org/10.1039/d6ra00243a
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