偶氮苯
恶二唑
抗真菌
化学
组合化学
有机化学
生物
分子
微生物学
作者
Wen Fu,Qinglong Yuan,Hongti Zhang,Xiaoyan Li,Yiming Lu,Wenming Yan,Yonghao Ye,Xili Liu,Zhong Li,Xusheng Shao
标识
DOI:10.1021/acs.jafc.4c05500
摘要
Azo-incorporating was reported to be an effective strategy for increasing SDH inhibitory activity but for poor in vivo control effects. Herein, the azo-incorporated compounds were structurally optimized to retain a preferential conformation by replacing the azo bond with their bioisosteres. Interestingly, the 1,2,4-oxadiazole compound
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