首页> 外文期刊>Journal of Agricultural and Food Chemistry >Triazolopyrimidines as a New Herbicidal Lead for Combating Weed Resistance Associated with Acetohydroxyacid Synthase Mutation
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Triazolopyrimidines as a New Herbicidal Lead for Combating Weed Resistance Associated with Acetohydroxyacid Synthase Mutation

机译:Triazolopyrimidines作为抗除草剂与乙酰羟酸合酶突变相关的新除草剂。

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摘要

Acetohydroxyacid synthase (AHAS; also known as acetolactate synthase; EC 2.2.1.6, formerly EC 4.1.3.18) is the first common enzyme in the biosynthetic pathway leading to the branched-chain amino acids in plants and a wide range of microorganisms. Weed resistance to AHAS-inhibiting herbicides, increasing at an exponential rate, is becoming a global problem and leading to an urgent demand of developing novel compounds against both resistant and wild AHAS. In the present work, a series of novel 2-aroxyl-1,2,4-triazolopyrimidine derivatives (a total of 55) were designed and synthesized with the aim to discover an antiresistant lead compound. Fortunately, the screening results indicated that many of the newly synthesized compounds showed a better, even excellent, inhibition effect against both the wild-type Arabidopsis thaliana AHAS and P197L mutants. Among them, compounds 5-3 to 5-17, compounds 5-19 to 5-26, compounds 5-28 to 5-45, and compound 5-48 have the lower values of resistance factor (RF) and display a potential power to overcome resistance associated with the P197L mutation in the enzyme levels. Further greenhouse in vivo assay showed that compounds 5-15 and 5-20 displayed "moderate" to "good" herbicidal activity against both the wild type-and the resistant (P197L mutation) Descurainia sophia, even at a rate as low as 0.9375 (g of ai/ha). The above results indicated that these two compounds could be used as new leads for the future development of antiresistance herbicides.
机译:乙酰羟酸合酶(AHAS;也称为乙酰乳酸合酶; EC 2.2.1.6,以前称为EC 4.1.3.18)是生物合成途径中导致植物和多种微生物中的支链氨基酸的第一种常见酶。杂草对抑制AHAS的除草剂的耐药性正呈指数级增长,这已成为一个全球性问题,并迫切需要开发出针对耐药和野生AHAS的新型化合物。在本工作中,设计并合成了一系列新颖的2-芳氧基-1,2,4-三唑并嘧啶衍生物(共55种),目的是发现一种抗药性的先导化合物。幸运的是,筛选结果表明,许多新合成的化合物对野生型拟南芥AHAS和P197L突变体均表现出更好,甚至更好的抑制作用。其中,化合物5-3至5-17,化合物5-19至5-26,化合物5-28至5-45和化合物5-48具有较低的电阻因子(RF)值,并显示出潜在功率克服与酶水平的P197L突变相关的抗性。进一步的温室体内试验表明,化合物5-15和5-20对野生型和抗性(P197L突变)地衣藻均显示出“中度”到“良好”的除草活性,即使其比率低至0.9375(克/公顷)。以上结果表明,这两种化合物可以作为抗性除草剂未来发展的新线索。

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