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作 者:叶久辉 桂阔 殷妮 刘新 李璇 雷鹏 冯俊涛 马志卿 高艳清 YE Jiuhui;GUI Kuo;YIN Ni;LIU Xin;LI Xuan;LEI Peng;FENG Juntao;MA Zhiqing;GAO Yanqing(College of Plant Protection,Northwest A&F University,Shaanxi Research Center of Biopesticide Engineering&Technology,Yangling 712100,Shaanxi Province,China)
机构地区:[1]西北农林科技大学植物保护学院,陕西省生物农药工程技术研究中心,陕西杨凌712100
出 处:《农药学学报》2024年第3期462-471,共10页Chinese Journal of Pesticide Science
基 金:国家重点研发计划项目(2023YFD1701200);陕西省重点研发计划项目(2024NC-YBXM-255);大学生创新创业训练计划项目(S202310712245)。
摘 要:为了丰富天然单萜桧木醇的结构多样性、拓宽其活性范围,在前期研究的基础上,以桧木醇为先导化合物,设计并合成了15个新型桧木醇羧酸酯类化合物(3)以及20个桧木醇磺酸酯类化合物(异构体5和6)。抑菌活性测定结果表明,大部分目标化合物在50μg/mL下对苹果树腐烂病菌Valsa mali、水稻纹枯病菌Rhizoctonia solani、番茄灰霉病菌Botrytis cinerea及黄瓜炭疽病菌Colletotrichum orbiculare均表现出良好的抑菌活性,其中羧酸酯类衍生物3a、3f、3g、3o对水稻纹枯病菌的EC50值分别为0.96、1.05、1.29和1.88μg/mL,3a、3e、3j对苹果树腐烂病菌的EC50值分别为3.60、3.28和3.48μg/mL,3d、3f、3g对黄瓜炭疽病菌的EC50值分别为0.77、0.51和0.67μg/mL,均优于桧木醇。总体来说,羧酸酯类衍生物的抑菌活性明显优于磺酸酯类衍生物,但磺酸酯类衍生物酯基位置的异构体抑菌活性存在较大差异,构型为1时抑菌活性更好。As a continuous research on structure derivation and activity of natural monoterpenoid hinokitiol,15 novel hinokitol carboxylic acid esters(3)and 20 hinokitol sulfonate esters(isomers 5 and 6)were designed and synthesized from hinokitiol as a lead compound.The results of fungicidal activity showed that most of the target compounds at 50μg/mL exhibited good fungicidal activity against Valsa mali,Rhizoctonia solani,Botrytis cinerea,and Colletotrichum orbiculare.The EC50 values of 3a,3f,3g,3o against R. solani were 0.96, 1.05, 1.29 and 1.88 μg/mL, respectively, the EC50 values of 3a, 3e and 3j were 3.60, 3.28 and 3.48 μg/mL against V. mali, and the EC50 values of 3d, 3f and 3g were 0.77, 0.51 and 0.67 μg/mL against C. orbiculare, respectively, which were superior to hinokitol. In general, the fungicidal activity of carboxylate derivatives was significantly better than that of sulfonate derivatives. The position isomers of sulfonate derivatives possessed different fungicidal activities, among which the compound with configuration 1 has better activities.
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