Privileged fragment-based design, synthesis and in vitro antitumor activity of imatinib analogues
نویسندگان
چکیده
Based on the privileged fragment-based drug design strategy, a series of imatinib analogues bearing moiety 3-(2-amino- 2-oxoacetyl)-1H-indole were designed and synthesized, in vitro antitumor activity these compounds was detected by MTT method using K562 (human myeloid leukemia) K562R (imatinib-resistant chronic cell lines. Molecular docking used to preliminarily explain possible binding modes. The most potent compound I2 exhibited better than those against cancer cells with IC50 values 0.8 ?M 0.7 ?M.
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ژورنال
عنوان ژورنال: Turkish Journal of Chemistry
سال: 2023
ISSN: ['1300-0527', '1303-6130']
DOI: https://doi.org/10.55730/1300-0527.3549