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3-芳基-1,2,4-三嗪-6-酮衍生物的合成及其抗真菌活性

Synthesis and antifungal activity of 3-aryl-1,2,4-triazin-6-one derivatives.

作者信息

Owen W John, Sullenberger Michael T, Loso Michael R, Meyer Kevin G, Slanec Thomas J

机构信息

Dow AgroSciences, Indianapolis, IN, USA.

出版信息

Pest Manag Sci. 2015 Jan;71(1):83-90. doi: 10.1002/ps.3765. Epub 2014 Apr 1.

Abstract

BACKGROUND

As a result of resistance development in many plant-pathogenic fungi to agricultural fungicides, there is an ongoing need to discover novel antifungal chemistries to help sustain efficient crop production. A fungicide screening program identified 3-phenyl-1-(2,2,2-trifluoroethyl)-1,2,4-triazin-6(1H)-one (5) as a promising new starting point for further activity optimization. A series of analogs were designed, prepared and evaluated in growth inhibition assays using four plant-pathogenic fungi.

RESULTS

Thirty nine analogs (compounds 5 to 43) were prepared to explore structure-activity relationships at R1 and R2, and all targeted structures were characterized by (1)H NMR and MS. All compounds were in vitro tested against three ascomycetes [Leptosphaeria nodorum, Magnaporthe grisea and Zymoseptoria tritici (syn. Mycosphaerella graminicola)] and one basidiomycete (Ustilago maydis) pathogen. When R2 was trifluoroethyl, fungicidal activity was enhanced by a single electron-withdrawing substitution, such as Br, Cl and CF3 in the 3-position at R1 (compounds 9, 10 and 12), of which the 3-bromo compound (10) was the most active (EC50 = 0.08, averaged across four pathogens). More subtle activity improvement was found by addition of a second halogen substituent in the 4-position, with the 3-Br-4-F analog (20) being the most active against the commercially important cereal pathogen Z. tritici. Replacement of the R2 haloalkyl group with benzyl, alkyl (e.g. n-butyl, i-butyl, n-pentyl) and, particularly, CH2 -cycloalkyls (e.g. CH2-cyclopropyl, CH2-cyclobutyl) resulted in further activity enhancements against the ascomycete fungi, but was either neutral or detrimental to activity against U. maydis. One of the most active compounds in this series (41) gave control of Z. tritici, with an EC50 of 0.005 ppm, comparable with that of the commercial strobilurin fungicide azoxystrobin (EC50 0.002 ppm).

CONCLUSIONS

The present work demonstrated that the 3-phenyl-1,2,4-triazin-6-ones are a novel series of compounds with highly compelling levels of antifungal activity against agriculturally relevant plant-pathogenic fungi.

摘要

背景

由于许多植物致病真菌对农用杀菌剂产生了抗性,因此持续需要发现新型抗真菌化学物质以帮助维持高效作物生产。一项杀菌剂筛选计划确定3-苯基-1-(2,2,2-三氟乙基)-1,2,4-三嗪-6(1H)-酮(5)是进一步优化活性的有前景的新起点。设计、制备了一系列类似物,并使用四种植物致病真菌在生长抑制试验中对其进行了评估。

结果

制备了39种类似物(化合物5至43)以探索R1和R2处的构效关系,所有目标结构均通过(1)H NMR和MS进行了表征。所有化合物均针对三种子囊菌[小麦壳针孢、稻瘟病菌和小麦黄斑叶枯病菌(同义词:小麦球腔菌)]和一种担子菌(玉米黑粉菌)病原体进行了体外测试。当R2为三氟乙基时,通过在R1的3位进行单吸电子取代(如Br、Cl和CF3)(化合物9、10和12)可增强杀真菌活性,其中3-溴化合物(10)活性最高(EC50 = 0.08,四种病原体的平均值)。通过在4位添加第二个卤素取代基发现了更细微的活性改善,3-溴-4-氟类似物(20)对商业上重要的谷物病原体小麦黄斑叶枯病菌活性最高。用苄基、烷基(如正丁基、异丁基、正戊基),特别是CH2-环烷基(如CH2-环丙基、CH2-环丁基)取代R2卤代烷基导致对子囊菌真菌的活性进一步增强,但对玉米黑粉菌的活性要么无影响要么有害。该系列中活性最高的化合物之一(41)对小麦黄斑叶枯病菌的防治效果,EC50为0.005 ppm,与市售甲氧基丙烯酸酯类杀菌剂嘧菌酯(EC50 0.002 ppm)相当。

结论

目前的工作表明,3-苯基-1,2,4-三嗪-6-酮是一系列新型化合物,对农业相关植物致病真菌具有极具吸引力的抗真菌活性水平。

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