Discovery of novel carbazole derivatives containing a 1,3,4-thiadiazole moiety as antifungal candidates

IF 1.4 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
Chenghao Tang , Xingju Chen , Shengzhou Yang , Wenbo Guo , Xiumei Yang , Pei Li , Xiang Wang
{"title":"Discovery of novel carbazole derivatives containing a 1,3,4-thiadiazole moiety as antifungal candidates","authors":"Chenghao Tang ,&nbsp;Xingju Chen ,&nbsp;Shengzhou Yang ,&nbsp;Wenbo Guo ,&nbsp;Xiumei Yang ,&nbsp;Pei Li ,&nbsp;Xiang Wang","doi":"10.1080/10426507.2023.2191961","DOIUrl":null,"url":null,"abstract":"<div><p>Fifteen novel carbazole derivatives of 2-(9<em>H</em>-carbazol-9-yl)-<em>N</em>-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamide were designed, synthesized and evaluated for their antifungal activities against <em>Pellicularia sasakii</em> (<em>P. sasakii</em>), <em>Fusarium oxysporum</em> (<em>F. oxysporum</em>), <em>Gibberella zeae</em> (<em>G. zeae</em>), <em>Phytophthora infestans</em> (<em>P. infestans</em>), <em>Cytospora mandshurica</em> (<em>C. mandshurica</em>) and <em>Capsicum wilt</em> (<em>C. wilt</em>). The results of antifungal activity tests indicated that the inhibitory rates of compounds 2-(2-chloro-9<em>H</em>-carbazol-9-yl)-<em>N</em>-(5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl)acetamide (<strong>3h</strong>) and 2-(2-chloro-9<em>H</em>-carbazol-9-yl)-<em>N</em>-(5-(thiophen-2-yl)-1,3,4-thiadiazol-2-yl)acetamide (<strong>3o</strong>) against <em>P. sasakii</em> were 72.89% and 74.29%, respectively, which displayed better bioactivity compared with commercial fungicides hymexazol (53.09%) and carbendazim (69.65%). Meanwhile, compounds 2-(9<em>H</em>-carbazol-9-yl)-<em>N</em>-(5-(thiophen-2-yl)-1,3,4-thiadiazol-2-yl)acetamide (<strong>3f</strong>) and 2-(3-iodo-9<em>H</em>-carbazol-9-yl)-<em>N</em>-(5-(p-tolyl)-1,3,4-thiadiazol-2-yl)acetamide (<strong>3 l</strong>) exhibited the inhibition rates of 72.40% and 67.65% against <em>C. wilt</em>, respectively, which were better than the commercial fungicides hymexazol (50.21%) and carbendazim (65.33%).</p></div>","PeriodicalId":20056,"journal":{"name":"Phosphorus, Sulfur, and Silicon and the Related Elements","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phosphorus, Sulfur, and Silicon and the Related Elements","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1042650723000333","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

Fifteen novel carbazole derivatives of 2-(9H-carbazol-9-yl)-N-(5-phenyl-1,3,4-thiadiazol-2-yl)acetamide were designed, synthesized and evaluated for their antifungal activities against Pellicularia sasakii (P. sasakii), Fusarium oxysporum (F. oxysporum), Gibberella zeae (G. zeae), Phytophthora infestans (P. infestans), Cytospora mandshurica (C. mandshurica) and Capsicum wilt (C. wilt). The results of antifungal activity tests indicated that the inhibitory rates of compounds 2-(2-chloro-9H-carbazol-9-yl)-N-(5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl)acetamide (3h) and 2-(2-chloro-9H-carbazol-9-yl)-N-(5-(thiophen-2-yl)-1,3,4-thiadiazol-2-yl)acetamide (3o) against P. sasakii were 72.89% and 74.29%, respectively, which displayed better bioactivity compared with commercial fungicides hymexazol (53.09%) and carbendazim (69.65%). Meanwhile, compounds 2-(9H-carbazol-9-yl)-N-(5-(thiophen-2-yl)-1,3,4-thiadiazol-2-yl)acetamide (3f) and 2-(3-iodo-9H-carbazol-9-yl)-N-(5-(p-tolyl)-1,3,4-thiadiazol-2-yl)acetamide (3 l) exhibited the inhibition rates of 72.40% and 67.65% against C. wilt, respectively, which were better than the commercial fungicides hymexazol (50.21%) and carbendazim (65.33%).

发现含有1,3,4-噻二唑片段的新型咔唑衍生物作为抗真菌候选物
设计、合成了15种新的2-(9H-咔唑-9-基)-N-(5-苯基-1,3,4-噻二唑-2-基)乙酰胺咔唑衍生物,并对其对沙氏Pellicularia sasakii(P.sasakiii)、尖孢镰刀菌(F.oxysporum)、玉米赤霉(G.zeae)、晚疫霉(P.infestans)、水曲柳(C.mandshurica)和辣椒枯萎病(C.wilt)的抗真菌活性进行了评价。抗真菌活性试验结果表明,化合物2-(2-氯-9H-咔唑-9-基)-N-(5-(4-氟苯基)-1,3,4-噻二唑-2-基)乙酰胺(3h)和2-(2-氟-9H-咔嗪-9-基]-N-(-5-(噻吩-2-基)-1,3,4噻二唑2-基)乙胺(3o)对日本稻瘟病菌的抑制率分别为72.89%和74.29%,与市售杀菌剂hymexazol(53.09%)和多菌灵(69.65%)相比,其表现出更好的生物活性 l) 对枯萎病的抑制率分别为72.40%和67.65%,优于市售杀菌剂处女膜唑(50.21%)和多菌灵(65.33%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信