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内型异莰烷基甲醛缩氨基硫脲类化合物的合成及抑菌活性
Synthesis and Antifungal Activity of Endo-isocamphanyl-formaldehyole Thiosemicarbazides
【摘要】 以莰烯衍生物内型异莰烷基甲醛与氨基硫脲衍生物进行缩合反应,合成了5种缩氨基硫脲类化合物(3a~3e),并通过IR、MS、1H NMR和13C NMR等分析方法对其结构进行了表征。采用菌丝生长速率法测试了化合物3a~3e对水稻纹枯病菌等8种植物病原菌的生长抑制作用,结果表明:5种化合物中,内型异莰烷基甲醛缩氨基硫脲(3a)对8种植物病原菌的抑制率最高,在质量浓度为50 mg/L时,3a对油茶炭疽病菌、枇杷炭疽病菌的抑制率分别为91.9%和97.2%,对油茶果生刺盘孢菌和彩绒革盖菌的抑制率均达100%,对水稻纹枯病菌、松枯梢病病原菌和西瓜枯萎病菌的抑制率分别为80.7%、 79.8%、 79.5%,均优于阳性对照样百菌清。
【Abstract】 5 endo-isocamphanyl-formaldehyole thiosemicarbazide compounds(3a-3e) were synthesized by condensation reactions of camphene derivatives endo-isocamphanyl-formaldehyole with thiosemicarbazide derivatives. Their structures were characterized by IR, MS, 1H NMR and 13C NMR. The mycelial growth rate method was used to study the inhibition effects of the related compounds on the growth of 8 plant pathogenic fungi including Rhizoctonia solani. The results showed that, among 5 compounds, the inhibition rate of endo-isocamphanyl-formaldehyole thiosemicarbazide(3a) was the highest against 8 plant pathogenic fungi. At the mass concentration of 50 mg/L, the inhibition rates of 3a against Colletotrichum gloeosporioides and Colletotrichum acutatum were 91.9% and 97.2%, respectively. The inhibition rates of 3a against Colletotrichum fructicola and Coriolus versicolor were both 100%. The inhibition rates of 3a against Rhizoctonia solani, Sphaeropsis sapinea and Fusariumoxyporum f. sp. niveum were 80.7%, 79.8% and 79.5%, respectively, which were better than that of the positive control sample of Chlorothalonil.
【Key words】 endo-isocamphanyl-formaldehyole; thiosemicarbazide; condensation reaction; structural analysis; antifungal activity;
- 【文献出处】 林产化学与工业 ,Chemistry and Industry of Forest Products , 编辑部邮箱 ,2024年01期
- 【分类号】TQ455
- 【下载频次】30