Insecticidal activities and chemical components of alcohol extract from leaves of Rhodendron dauricu Insecticidal activities and chemical components of alcohol extract from leaves of Rhodendron dauricu

Insecticidal activities and chemical components of alcohol extract from leaves of Rhodendron dauricu

  • 期刊名字:林业研究(英文版)
  • 文件大小:
  • 论文作者:SUN Mo-long,WANG Tian-miao
  • 作者单位:College of Science,School of Chemistry and Molecular Engineering
  • 更新时间:2022-12-26
  • 下载次数:
论文简介

The extract from leaves of Rhododendron dauricum L. was extracted with 95% alcohol by common method for studying its insecti-cidal activities. The chemical components of the alcohol extract and relative contents were analyzed by GC-MS. The insecticidal activities of the alcohol extract were tested on the 2nd-3rd instar larvae of Lymantria dispar L. for five days. Five concentrations of the extract samples were designed as 50, 10, 5, 1, and 0.5 g·L-1. The results show that the alcohol extracts from leaves of R. dauricum exhibited insecticidal activities against larvae of L. dispar. The corrected mortality of larvae of L. dispar for was over 50% for both contact toxicity and stomach toxicity at the extract concentration of ≥ 5 g·L-1 after five days of application. The insecticidal activity in contact toxicity is more effect than stomach toxic-ity for the alcohol extract. Twenty compounds, with total GC relative contents of 93.81% in the alcohol extract from leaves of R. dauricum were identified. The main chemical components in the extract are: (1) 4,5-Dihydro-5-oxo-3-(p-tolyl) isoxazole, with a relative content of 40.03%; (2) 1,3-Benzenediol, 5-methyl-2-(3,7,11-trimethyl-2,6,10-dodecatrienyl)-, (E,E)-, the relative content 18.27%; (3) 3,6-Diphenyl-1,2,3,4,5,6,7,8-octahydro-1,8-acridinedione, the relative content 3.89%; (4) 6H-[1,2,4]Triazolo[1,5-a]indole, 4a,5,7,8,8a,9-hexahydro-9-methylene-, the relative content 2.99%; (5) 7-Amino-4-methyl-1,8-naphthyridin-2-ol, the relative content 2.64%; (6) 4-Methyl-2,6-dihydroxyquinoline, the relative content 2.63%; (7) 2,4,6-Triaminoquinazoline, the relative content 2.27%; (8) 2(1H)-Quinolinone, 4-hydroxy-1-methyl-, the relative content 2.02%.

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