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首页> 外文期刊>Acta Chimica Slovenica >Synthesis and in vitro Study of Some New Bis(thiadiazolyl-2H-pyrazolo[3,4-d][1,3]thiazole)- methanes as Potential Nematicides
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Synthesis and in vitro Study of Some New Bis(thiadiazolyl-2H-pyrazolo[3,4-d][1,3]thiazole)- methanes as Potential Nematicides

机译:新型双(噻二唑-2H-吡唑并[3,4-d] [1,3]噻唑)-甲烷作为潜在杀线虫剂的合成及体外研究

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摘要

A new series of bis(pyrazolo[3,4-d][1,3]thiazoles) 7a-j has been synthesized and characterized via IR,~1H NMR,~(13)C NMR, MS and elemental analyses. All the newly synthesized compounds 7a-j have been assayed for their nematicidal activity against Ditylenchus myceliophagus and Caenorhabditis elegans by aqueous in vitro screening technique. The screened data reveal that the compound 7e is most effective against D. myceliophagus and C. elegans with LD_(50) of 160 and 180 ppm respectively and is almost equal to the activity of the standard levamisole. The compounds 7h and 7j are also most active against C. elegans with LD_(50) of 190 ppm and D. myceliophagus with LD_(50) of 180 ppm, respectively. Further, 7a-j were screened for their antibacterial activity. Most of these new compounds showed potent activity against the test bacteria and emerged as potential molecules for further development.
机译:合成了一系列新的双(吡唑并[3,4-d] [1,3]噻唑)7a-j,并通过IR,〜1H NMR,〜(13)C NMR,MS和元素分析对其进行了表征。已经通过水性体外筛选技术测定了所有新合成的化合物7a-j针对杀线粒体菌丝体和秀丽隐杆线虫的杀线虫活性。筛选的数据表明,化合物7e的LD_(50)分别为160和180 ppm,对D. myceliophagus和秀丽隐杆线虫最有效,并且几乎等于标准左旋咪唑的活性。化合物7h和7j分别对线虫的线虫(LD_(50)为190ppm)和食丝线虫的线虫(LD_(50)为180ppm)最具活性。此外,筛选了7a-j的抗菌活性。这些新化合物中的大多数显示出对测试细菌的有效活性,并以潜在的分子形式出现,可供进一步开发。

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