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- W4297183107 abstract "A series of thiophene derivatives substituted at 2, 3 and 5 positions were designed and synthesized using 2,3-disubstituted thiophene aldehyde and alcohol as key building blocks. Invitro cytotoxicity assessed against PC-3, DU145 (prostate), A549 (lung), HT29, HCT116 (colon), MCF7, MDAMB231 (breast), B16F10 (melanoma) NCI (Colorectal) cancer cell lines by conducting (MTT) assay of thiophene derivatives. Most of these synthesized compounds showed anti-cancer activity, compound 5b showed good cytotoxicity with IC50 = 2.61 ± 0.34 µM on HT29 cell line. Also, the key property of cell migration was observed while treating cells with 5b. The Cell cycle arrest at G2/M phase was observed by 5b on HT29 cell line which inhibited tubulin polymerization with IC50 value of 8.21 ± 0.30 μM. Moreover, binding pose with co-crystal ligand and interaction with colchicine binding site of 5b was established by molecular docking studies. Hence this scaffold can be developed as anti-cancer agents that target tubulin polymerization." @default.
- W4297183107 created "2022-09-27" @default.
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- W4297183107 date "2022-09-23" @default.
- W4297183107 modified "2023-09-30" @default.
- W4297183107 title "Design, synthesis and molecular docking study of thiophenyl hydrazone derivatives as tubulin polymerization inhibitors" @default.
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- W4297183107 doi "https://doi.org/10.1080/00397911.2022.2125324" @default.
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