Unlock instant, AI-driven research and patent intelligence for your innovation.

Application of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound to pest control

A technology of dihydroxy carboxylic acid and gem difluoride, which is applied in the field of pesticides to achieve remarkable technological progress and excellent stomach toxicity

Inactive Publication Date: 2015-02-18
SHANGHAI INST OF TECH
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these pesticides are all juvenile hormone analogs in chemical structure, and there is a possibility of cross-resistance

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Application of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound to pest control
  • Application of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound to pest control
  • Application of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound to pest control

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Example 1 Test of the inhibitory effect of compounds of formula I on JH biosynthesis.

[0021] The present invention adopts the in vitro radiochemical method invented by Professor Tobe et al. to test the activity of all compounds for inhibiting juvenile hormone biosynthesis.

[0022] Test insects and reagents:

[0023] The test insects were five-instar tobacco hornworm moth (Manduca sexta) larvae that had just shed their skin.

[0024] L-[ 14 C-S-methyl]-methionine, purchased from Amersham Company, culture medium M199 (1.3 mM Ca 2+ , 2% Ficoll, without methionine), purchased from GIBCO.

[0025] Experimental steps:

[0026] (1) Microanatomy of CA

[0027] Anesthetize the Manduca sexta moth with ice, place it on a wax plate, open the neck membrane with clock forceps near the head of the insect, take out the CA, and remove the surrounding connective tissue in M199 for bioassay.

[0028] (2) In vitro bioassay

[0029] One CA was placed in 100 μL of M199 containing 4...

Embodiment 2

[0037] Example 2 Test of the stomach toxicity effect of the compound of formula I on pests.

[0038] Refer to "Pesticide Indoor Bioassay Test Guidelines Insecticides Part 2: Stomach Toxicity Activity Test-Poisoned Leaf Method" (NY / T 1154.2-2006).

[0039] (1) Test material

[0040] The test insects were the larvae of the second-instar tobacco hornworm (Manduca sexta) that had just shed their skin. Leaf discs were made from young leaves of tobacco (Nicotiana tabacum L.).

[0041] (2) Test method

[0042] Gastric toxicity test was carried out by using the poisoned leaf method, and the mortality rate was checked after 24 hours of drug treatment. As a result, it was found that some of the compounds of formula I had gastric toxicity to Manduca sexta larvae, among which compounds 7, 19 and 20 were the best (Table 2).

[0043] Table 2 Compounds have gastric toxicity to Manduca sexta larvae

[0044]

[0045]

Embodiment 3

[0046] Example 3 Test of the ovicidal effect of the compound of formula I on pests.

[0047] Refer to "Indoor Bioassay Test Guidelines for Pesticides Insecticides Part 5: Immersion Method for Ovicidal Activity Test" (NY / T1154.5-2006).

[0048] (1) Test material

[0049] Fresh eggs of Manduca sexta were collected.

[0050] (2) Test method

[0051] Tested by immersion method. After the eggs were immersed in the medicinal solution for 10 seconds, they were transferred to culture under normal conditions. The corresponding organic solvent treatment without medicament was set as the control. Calculate the hatch inhibition rate. As a result, it was found that some compounds of formula I had ovicidal activity on Manduca sexta larvae, among which compounds 7, 19 and 20 were the best (Table 3).

[0052] Table 3 Compounds have ovicidal effect on Manduca sexta

[0053]

[0054]

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides the application of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound to pest control. The structural formula of 4 gem-Gem-difluoromethylene substituted 3, 5 dyhydroxyl polycarboxylic compound is shown in the figure I , wherein, R1 is an aromatic group, and R2 is alkyl, a hydrogen atom or alkali metal and an alkaline earth cation. The compound belongs to excellent juvenile hormone biosynthesis inhibitors, and the median inhibitory concentration reaches nanomole per litre. The in vivo insecticidal activity is mainly embodied in excellent stomach toxicity, ovicidal and insect growth regulation effects.

Description

technical field [0001] The invention belongs to the field of pesticides, and in particular relates to a 3,5 dihydroxy carboxylic acid compound substituted with a 4-gem difluoride, especially the application of the 3,5 dihydroxy carboxylic acid compound substituted with a 4-gem difluoride in pest control. Background technique [0002] Pesticides play an irreplaceable role in the prevention and control of agricultural pests and sanitary pests, and are an important guarantee for agricultural harvests and human health. [0003] Juvenile hormone (JH) is an important class of insect hormones. It regulates the growth and development of immature insects and the reproduction of adults. Scientists have developed a large series of insect growth regulators (IGRs) - juvenile hormone analogues by using JH as the lead. The main varieties of existing juvenile hormone analogues are: methoprene, triprene, hydroprene, kinoprene, fenoxycard, Pyriproxyfen (pyriproxyfen) and pyridoxone (NC-170...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A01N43/56A01N43/38A01N37/36A01N37/38A01N43/16A01N43/42A01P7/04
Inventor 开振鹏吴范宏李媛媚王志臧洋洋
Owner SHANGHAI INST OF TECH