Synthesis, in vitro antitumor activity and molecular modeling studies of a new series of benzothiazo

来源 :Chinese Chemical Letters | 被引量 : 0次 | 上传用户:ihwfihwf
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A new series of benzothiazole Schiff bases 3–29 was synthesized and screened for antitumor activity against cervical cancer(Hela) and kidney fibroblast cancer(COS-7) cell lines. Results indicated that compounds 3, 14, 19, 27 and 28 have promising activity against Hela cell line with IC_(50) values of 2.41,3.06, 6.46, 2.22 and 6.25 mmol/L, respectively, in comparison to doxorubicin as a reference antitumor agent(IC_(50) 2.05 mmol/L). In addition, compound 3 displayed excellent activity against COS-7 cell line with IC_(50) value of 4.31 mmol/L in comparison to doxorubicin(IC_(50)3.04 mmol/L). In the present work,structure based pharmacophore mapping, molecular docking, protein-ligand interaction, fingerprints and binding energy calculations were employed in a virtual screening strategy to identify the interaction between the compounds and the active site of the putative target, EGFR tyrosine kinase. Molecular properties, toxicity, drug-likeness, and drug score profiles of compounds 3, 14, 19, 27, 28 and 29 were also assessed. A new series of benzothiazole Schiff bases 3-29 was synthesized and screened for antitumor activity against cervical cancer (Hela) and kidney fibroblast cancer (COS-7) cell lines. Results indicated that compounds 3, 14, 19, 27 and 28 are promising activity against Hela cell line with IC 50 values ​​of 2.41, 3.06, 6.46, 2.22 and 6.25 mmol / L, respectively, in comparison to doxorubicin as a reference antitumor agent (IC 50 (2.05 mmol / L) Compound 3 displayed excellent activity against COS-7 cell line with IC 50 value of 4.31 mmol / L in comparison to doxorubicin (IC 50 (50) 3.04 mmol / L). In the present work, structure based pharmacophore mapping, molecular docking, protein-ligand interaction, fingerprints and binding energy calculations were employed in a virtual screening strategy to identify the interaction between the compounds and the active site of the putative target, EGFR tyrosine kinase. Molecular properties, toxicity, drug-likeness, and drug score profiles of compounds 3, 14, 19, 27, 28 and 29 were also assessed.
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