Design, synthesis and antiproliferative activity evaluation of new 3,7-disubstituted pyrrolo[2,3-c]pyridines

A number of 3,7-disubstituted 6-azaindoles were designed and synthesized starting from the readily accessible 2-chloro-3-nitro-4-picoline. The target compounds were tested for their antiproliferative activity against HT-1080, A431 and A549 cancer cell lines in comparison to the normal human AG01523 strain. The 3-acetyl-7-anilino derivative exerts a substantial selective cytotoxic effect towards cancer cells at the low μM range, causing a G2/M-phase arrest and apoptosis. • Synthesis and full characterization of novel 3,7-disubstituted pyrrolo[2,3- c ]pyridines derivatives is described. • In vitro cytotoxic activity on cancer cell lines HT-1080, A431 and A549, and activity against normal AG01523 cells is provided. • Structure-activity relationships are extracted pointing out the most favorable substitution pattern. • Cell cycle phase distribution on HT-1080 cells showed that the most active derivatives induce G2/M-phase arrest.

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Publication Details

Journal
European Journal of Medicinal Chemistry Reports
Published
2026-02-17
DOI
https://doi.org/10.1016/j.ejmcr.2026.100328
Primary Topic
Synthesis and Reactivity of Heterocycles
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article
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article

Design, synthesis and antiproliferative activity evaluation of new 3,7-disubstituted pyrrolo[2,3-c]pyridines

Maria Georgiou, Eleni Mavrogonatou, Eleni V. Mikropoulou, Panagiotis Marakos et al.
European Journal of Medicinal Chemistry Reports
Synthesis and Reactivity of Heterocycles
article

Design, synthesis and antiproliferative activity evaluation of new 3,7-disubstituted pyrrolo[2,3-c]pyridines

Maria Georgiou, Eleni Mavrogonatou, Eleni V. Mikropoulou, Panagiotis Marakos, Dimitris Kletsas, Harris Pratsinis, Nicole Pouli, Nikolaos Lougiakis, Maria Halabalaki, Marianthi Zografistou
article en

Abstract

A number of 3,7-disubstituted 6-azaindoles were designed and synthesized starting from the readily accessible 2-chloro-3-nitro-4-picoline. The target compounds were tested for their antiproliferative activity against HT-1080, A431 and A549 cancer cell lines in comparison to the normal human AG01523 strain. The 3-acetyl-7-anilino derivative exerts a substantial selective cytotoxic effect towards cancer cells at the low μM range, causing a G2/M-phase arrest and apoptosis. • Synthesis and full characterization of novel 3,7-disubstituted pyrrolo[2,3- c ]pyridines derivatives is described. • In vitro cytotoxic activity on cancer cell lines HT-1080, A431 and A549, and activity against normal AG01523 cells is provided. • Structure-activity relationships are extracted pointing out the most favorable substitution pattern. • Cell cycle phase distribution on HT-1080 cells showed that the most active derivatives induce G2/M-phase arrest.

European Journal of Medicinal Chemistry ReportsVol. 16
National and Kapodistrian University of Athens (GR), National Centre of Scientific Research "Demokritos" (GR)
Openalex Percentile: Top 50%
Synthesis and Reactivity of Heterocycles
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Design, synthesis and antiproliferative activity evaluation of new 3,7-disubstituted pyrrolo[2,3-c]pyridines — Maria Georgiou, Eleni Mavrogonatou, et al. · European Journal of Medicinal Chemistry Reports (2026) | TGRS Research Map | TGRS