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AJBLS · Lens · Experimental and Computational Data on Indazole-Pyridine Derivatives: Synthesis, Characterization, and Anticancer Evaluation

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Article · Volume 15, Issue 2 · pp. 559–566

Experimental and Computational Data on Indazole-Pyridine Derivatives: Synthesis, Characterization, and Anticancer Evaluation

Kinjal Parmar1, Ishan Panchal2

  1. 1Faculty of Pharmacy, Parul University, Limda, Waghodia, Vadodara, Gujarat, INDIA.
  2. 2Department of Pharmaceutical Chemistry, Parul College of Pharmacy and Research, Faculty of Pharmacy, Parul University, Bopal, Ahmedabad, Gujarat, INDIA.

Abstract

Introduction: Breast cancer remains a major cause of cancer-related mortality among women worldwide, highlighting the need for novel therapeutic agents. Materials and Methods: Two indazole-pyridine derivatives (7i and 7j) were synthesized and characterized using FTIR, ¹H-NMR, ¹³C-NMR, and mass spectrometry. Molecular docking was performed to evaluate binding interactions. In vitro cytotoxicity against the MCF-7 cell line was assessed using the SRB assay (10-80 µg/mL). Results: Docking studies indicated stable ligand-receptor interactions. Both compounds exhibited dose-dependent cytotoxicity. Compound 7j showed strong antiproliferative activity (GI₅₀<10 µg/mL), while compound 7i showed moderate activity (GI₅₀=33.6 µg/mL). Conclusion: The presence of a pyrrolidine moiety in 7j enhances activity. These derivatives represent promising scaffolds for further optimization as anticancer agents.

Keywords: Indazole-Pyridine Derivatives; MCF-7 cell line; Molecular Docking; Structure-activity Relationship

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