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. 2023 Jan 23;14:1111912. doi: 10.3389/fphar.2023.1111912

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Copyright © 2023 Hu, Zhai, Tan, Chen, Zhang, Tan, Zheng, Gao, Wei, Wu and Yang.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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HQ, FMNT and CS significantly inhibited the viability of HT29 and Caco2 cells. The cytotoxicity of HQ (3.125–100 mg/mL, 48 h) (A and B), FMNT (3.125–200 μM, 48 h) (C and D) and CS (3.125–200 μM, 48 h) (E and F) toward HT29 and Caco2 cells, respectively. 5-FU was used as a positive control for inhibition of cell viability. The data represent the mean ± SD (n = 3). ^* p < 0.05 and ^*** p < 0.001 compared with the control group.