作者:Xiao-Feng Bao、Yi-Xin Zhu、Wen-Xia Xie、Zi-Yi Liu、Li Zhu、He Jiang、Yu Zhao
DOI:10.1080/10286020.2021.1982909
日期:2022.9.2
Abstract A novel series of 1-substituted phenazines 4a-4l were designed and synthesized via Palladium-catalyzed reactions from 1-phenazine trifluoromethanesulfonate. These phenazines showed antichlamydial activity with IC50 values from 1 to 10 μM. Among them, compounds 4c and 4i exhibited the best antichlamydial activity with IC50 values from 2.06 to 2.74 μM without apparent cytotoxicity to host cells
摘要 设计并通过钯催化的 1-吩嗪三氟甲磺酸盐反应合成了一系列新型 1-取代吩嗪4a - 4l 。这些吩嗪显示出抗衣原体活性,IC 50值为 1 至 10 μM。其中,化合物4c和4i表现出最好的抗衣原体活性,IC 50值从2.06到2.74 μM,对宿主细胞没有明显的细胞毒性。