抗真菌
琥珀酸脱氢酶
杀菌剂
化学
组合化学
铅化合物
立体化学
生物化学
生物
酶
体外
微生物学
植物
作者
Yan-Ming Yin,Xiaoming Zhang,Xiao-Yue Shang,Zihan Gao,Zheng-Bei Liang,Dawei Wang,Zhen Xi
标识
DOI:10.1021/acs.jafc.4c01739
摘要
Succinate dehydrogenase (SDH) has been considered an ideal target for discovering fungicides. To develop novel SDH inhibitors, in this work, 31 novel benzothiazol-2-ylthiophenylpyrazole-4-carboxamides were designed and synthesized using active fragment exchange and a link approach as promising SDH inhibitors. The findings from the tests on antifungal activity indicated that most of the synthesized compounds displayed remarkable inhibition against the fungi tested. Compound
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