Design, synthesis, and cytotoxicity evaluation of 1,2,3-triazole-linked β-carboline–benzimidazole hybrids as tubulin polymerization inhibitors

A series of 1,2,3-triazole-linked β-carboline–benzimidazole hybrids were designed, synthesized and evaluated for their cytotoxic potential. Compounds 14d and 14o exhibited potent cytotoxicity against MCF-7 and tubulin polymerization inhibition.

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Publication Details

Journal
New Journal of Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5nj03098f
Primary Topic
Synthesis and bioactivity of alkaloids
Type
article
Field-Weighted Citation Impact
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article

Design, synthesis, and cytotoxicity evaluation of 1,2,3-triazole-linked β-carboline–benzimidazole hybrids as tubulin polymerization inhibitors

Mursalim Ali Khan, Chandraiah Godugu, Nagula Shankaraiah, Anamika Sharma et al.
New Journal of Chemistry
Synthesis and bioactivity of alkaloids
article

Design, synthesis, and cytotoxicity evaluation of 1,2,3-triazole-linked β-carboline–benzimidazole hybrids as tubulin polymerization inhibitors

Mursalim Ali Khan, Chandraiah Godugu, Nagula Shankaraiah, Anamika Sharma, Preethi K. Raman, Naveen Chand Rallabandi
article en

Abstract

A series of 1,2,3-triazole-linked β-carboline–benzimidazole hybrids were designed, synthesized and evaluated for their cytotoxic potential. Compounds 14d and 14o exhibited potent cytotoxicity against MCF-7 and tubulin polymerization inhibition.

New Journal of ChemistryVol. 49(40)
National Institute of Pharmaceutical Education and Research - Ahmedabad (IN), National Institute of Pharmaceutical Education and Research (IN)
Openalex Percentile: Top 77%
Synthesis and bioactivity of alkaloids
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