共查询到20条相似文献,搜索用时 140 毫秒
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为了寻找结构新颖、杀菌活性更好的绿色农药。选用天然产物香草醛作为基本原料,引入五元杂环异■唑结构,首次设计并合成了28个香草醛异■唑类衍生物。结构经核磁共振氢谱、碳谱及高分辨质谱分析确认。测试了所有目标衍生物对烟草灰霉病菌(Botrytis cinerea)、层出镰刀菌(Fusarium proliferatum)、木贼镰刀菌(Fusarium equiseti)、玉米圆斑病菌(Bipolaris zeicola)、胶胞炭疽菌(Colletotrichum gloeosporioides)、草茎点霉菌(Phoma herbarum)6种广谱菌的杀菌活性。杀菌活性测定结果显示:在50μg/mL质量浓度下,部分化合物对6种真菌的菌丝生长均具有一定抑制作用,2-甲氧基-4-(5-苯基异■唑-3-基)苯乙酸酯对6种真菌的抑菌活性整体良好,对玉米圆斑病菌等3种菌的抑菌活性超过对照组百菌清;2-甲氧基-4-(5-(4-乙基苯基)异唑-3-基)苯酚对烟草灰霉病菌的抑菌活性最高,抑菌率可以达到93%。初步构效关系表明,对活性片段香草醛上的酚羟基进行乙酰化衍生,有助于提高化合物对6种病原菌的抑菌活性,为... 相似文献
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为了研究2-(N-苯磺酰基吲哚-3-基)-3-N-酰基-5-苯基-1,3,4-噁唑啉类化合物中具有潜在应用价值的抑菌先导化合物。在0.1 g/L质量浓度下,采用菌丝生长速率法测定了14种2-(N-苯磺酰基吲哚-3-基)-3-N-酰基-5-苯基-1,3,4-唑啉类化合物对小麦赤霉病菌、白菜黑斑病菌、棉花枯萎病菌、水稻稻瘟病菌和烟草赤星病菌的室内抑菌活性。结果表明,化合物1~化合物14对所测5种植物病原菌均表现出不同程度的抑菌活性,其中化合物9和化合物14对小麦赤霉病菌、白菜黑斑病菌、棉花枯萎病菌、水稻稻瘟病菌和烟草赤星病菌5种植物病原菌活性较好,其抑制率分别为15.69%~31.08%和16.28%~29.41%,表现出一定的广谱抑菌活性。初步拟定将这2个化合物作为进一步衍生修饰的先导化合物。 相似文献
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[目的]寻找新杀菌活性的苯联三唑(磺)酰胺衍生物。[方法]设计合成了系列N-(4-(3-苯基-1H-1,2,4-三唑-1-基)苯基)苯磺酰胺或苯甲酰胺衍生物,以菌丝生长速率法对其抑菌活性进行了初步评价。[结果]合成了3类12个N-(4-(3-苯基-1H-1,2,4-三唑-1-基)苯基)苯磺酰胺或苯甲酰胺衍生物,结构经1H及13C NMR确证。[结论]目标化合物收率为60.7%~81.3%;该类化合物对番茄灰霉病菌有较强抑制作用,其中11个化合物的抑菌率均大于85%,优于对照药剂烯唑醇(80.8%);5个化合物对苹果腐烂病菌的抑菌率大于74%,优于烯唑醇(68.6%)。 相似文献
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Abd El-Hamid N. Ahmed Mohamed A. Abd-Alla Maher F. El-Zohry 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1988,43(1):63-70
Several new quinazolin-4-one containing oxadiazolin-5-thione moieties were synthesized and evaluated for their antibacterial activity. Esterification of 2-substituted phenyl-3-carboxyalkyl-methyl-3,4-dihydroquinazolin-4-ones (I) with absolute ethyl alcohol in the presence of sulfuric acid afforded the corresponding esters (II). Hydrazinolysis of (II) with hydrazine hydrate in ethanol gave the acid hydrazides (III). Refluxing (III) with equimolar amounts of potassium hydroxide and slight excess of carbon disulfide afforded the corresponding oxadiazolin-5-thione derivatives (IV). The thiones undergo Mannich reaction using a formaldehyde/secondary amines mixture whereby the 4-substituted amino-methyl derivatives (V) were obtained. Microanalysis, IR, NMR spectra were used to elucidate the structures of the newly synthesized compounds. All the designed compounds were tested for their antibacterial activity. The morpholino derivatives showed an encouraging antibacterial activity. 相似文献
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Arban R Benedetti R Bonanomi G Capelli AM Castiglioni E Contini S Degiorgis F Di Felice P Donati D Fazzolari E Gentile G Marchionni C Marchioro C Messina F Micheli F Oliosi B Pavone F Pasquarello A Perini B Rinaldi M Sabbatini FM Vitulli G Zarantonello P Di Fabio R St-Denis Y 《ChemMedChem》2007,2(4):528-540
Two new classes of potent and selective CRF(1) receptor antagonists are presented. Exploration of general templates 3 and 4 through modifications of the top amine and bottom phenyl substituents led to optimization of the in vitro affinity and pharmacokinetic profiles. The typical alkyl chains present in the top region of CRF(1) antagonists were replaced by substituted heteroaryl moieties, leading to a dramatic improvement of the metabolic stability. This improvement was apparent when the compounds were dosed in vivo: several compounds exhibited low plasma clearance, good oral bioavailability, and high brain penetration. As a consequence of their outstanding pharmacokinetic profiles, these CRF(1) antagonists, as exemplified by compound 4 fi (4-(4-bromo-3-methyl-1H-pyrazol-1-yl)-7-(2,4-dichlorophenyl)-2-methyl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine), produced a dose-dependent "anxiolytic-like" effect when administered orally, decreasing the vocalization of rat pups. 相似文献
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杀菌剂唑菌酯的创制经纬 总被引:2,自引:2,他引:0
概述了运用中间体衍生化方法发现杀菌剂唑菌酯(SYP-3343)的过程:以取代吡唑环替换丁香菌酯结构中的香豆素环,设计并合成了一系列化合物,发现先导化合物(2),通过优化研究发现多个高活性化合物,最终发现了(E)-2-(2-((3-(4-氯苯基)-1-甲基-1H-吡唑-5-基氧基)甲基)苯基)-3-甲氧基丙烯酸甲酯,即唑菌酯(SYP-3343),其具有广谱的杀菌活性,对蔬菜和作物的多种病害如霜霉病、稻瘟病、白粉病、炭疽病等均有很好的防治效果,同时SYP-3343具有明显的杀虫、杀螨活性,可达到病虫兼治之目的。已于2009年获准临时登记。 相似文献
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The influence of mixtures of substituted phenols with sulphur compounds on the thermooxidative stability of polypropylene was studied. Following substituted phenols were used: 4,4′-butylidene-bis(3-methyl-6-tert.-butylphenol), 2,2′-methylidene-bis(4-methyl-6-tert.-butylphenol) and 4,4′-thio-bis(3-methyl-6-tert.-butylphenol). As sulphur compounds phenylalkylsulphides, p-nitrophenylalkylsulphides and some other p-substituted phenylsulphides were used. The effect of these mixtures was studied at 180°C in oxygen atmosphere. 相似文献
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3 取代苯基 5 羟基 5 三氟甲基异口恶唑啉是合成具有异口恶唑结构的原卟啉原氧化酶抑制剂类除草剂的重要中间体。通过以下途径制得4个具有不同取代基的异口恶唑啉中间体:首先,在回流状态,n(甲醇钠)∶n(取代苯乙酮)=2∶1的甲醇钠存在下,取代苯乙酮与三氟乙酸乙酯缩合得到取代苯基 4,4,4 三氟 1,3 丁二酮;后者可在室温下,于二氯甲烷溶剂中,用氯化硫酰氯化,在侧链上引入氯原子;最后,以乙酸作溶剂,回流下,具有不同取代基的苯基 1,3 丁二酮与盐酸羟胺闭环得到产物。反应总收率大于95%。产品结构经质谱、核磁共振氢谱、碳谱确认正确。 相似文献
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《Journal of Sulfur Chemistry》2013,34(5):445-453
1,3-Thiazolidine-2,4-dione 2 has been synthesized by the cyclisation reaction of thiourea and chloroacetic acid in the presence of ethanol. The reaction of compound 2 with substituted aromatic aldehyde afforded the corresponding derivatives of substituted 5-benzylidene-1,3-thiazolidinone-2,4-dione 3a–d, which upon reflux with ω-bromoalkoxyphthalimide gave 2-{[-5-(substituted benzylidine)-2,4-dioxo-1,3-thiazolidine-3-yl]alkoxy} -1H-isoindole-1,3(2H)-dione 4a–i. Further, compounds 4a–i were treated with phenyl hydrazine and 2,4 dinitro phenyl hydrazine in the DMF to yield the title compound 2-[5-oxo-2,3-substituted diphenyl-2H-pyrazolo[3,4-d][1,3]thiazol-6(5H)-yl)alkoxy]-1H-isoindole-1,3(2H)-dione 5a–r. Structures of newly synthesized compounds were established based on elemental analysis, IR, 1H NMR and mass spectral data. Synthesized compounds have been assayed for their antibacterial activities against B. subtilis, K. pneumoniae, P. aeruginosa and S. aureus and antifungal activities against A. fumigatus and C. albicans. 相似文献
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Rania Hamdy Arwyn T. Jones Mohamed El-Sadek Alshaimaa M. Hamoda Sarra B. Shakartalla Zainab M. AL Shareef Sameh S. M. Soliman Andrew D. Westwell 《International journal of molecular sciences》2021,22(22)
A series of 3-(6-substituted phenyl-[1,2,4]-triazolo[3,4-b]-[1,3,4]-thiadiazol-3-yl)-1H-indoles (5a–l) were designed, synthesized and evaluated for anti-apoptotic Bcl-2-inhibitory activity. Synthesis of the target compounds was readily accomplished through a reaction of acyl hydrazide (1) with carbon disulfide in the presence of alcoholic potassium hydroxide to afford the corresponding intermediate potassium thiocarbamate salt (2), which underwent cyclization reaction in the presence of excess hydrazine hydrate to the corresponding triazole thiol (3). Further cyclisation reaction with substituted benzoyl chloride derivatives in the presence of phosphorous oxychloride afforded the final 6-phenyl-indol-3-yl [1,2,4]-triazolo[3,4-b]-[1,3,4]-thiadiazole compounds (5a–l). The novel series showed selective sub-micromolar IC50 growth-inhibitory activity against Bcl-2-expressing human cancer cell lines. The most potent 6-(2,4-dimethoxyphenyl) substituted analogue (5k) showed selective IC50 values of 0.31–0.7 µM against Bcl-2-expressing cell lines without inhibiting the Bcl-2-negative cell line (Jurkat). ELISA binding affinity assay (interruption of Bcl-2-Bim interaction) showed potent binding affinity for (5k) with an IC50 value of 0.32 µM. Moreover, it fulfils drug likeness criteria as a promising drug candidate. 相似文献