As a continuation of our research on developing anticancer agents and based on the proven
proprieties of thieno[2,3‐b]pyridines as anticancer, we have designed to synthesize novel thieno[2,3‐
b]pyridine derivatives that incorporate different biologically active heterocycles through various
chemical reactions. All of the newly obtained compounds, compared with the standard anticancer
drug (doxorubicin), were screened in vitro for their antitumor activity against hepatocellular carcinoma
(HepG‐2) and human breast cancer (MCF‐7) cell lines. The results revealed that compounds 3, 7, 12,
and 19 were found to be the most potent against both HepG‐2 and MCF‐7 cell lines exhibiting IC50
values ranging from 3.67 to 11.50 and 5.13 to 11.80 μg/mL, respectively, among which compound 7
has a more potent activity than the reference drug doxorubicin against HepG‐2 cell line, showing IC50
value of 3.67 μg/mL (doxorubicin 4.65 μg/mL).

Author(s) Details

Aisha Y. Hassan
Department of Chemistry, Faculty of Science (Girls), Al‐Azhar University, Cairo, Egyp

Samiha A. ElSebaey
Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy (Girls), Al‐Azhar University, Cairo, Egypt.

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