Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Application of isoflavonoids compound to prepare agricultural bactericide

A technology for agricultural fungicides and compounds, which is applied in the field of preparing agricultural fungicides to achieve the effects of excellent bacteriostatic effect, environmental safety and wide application prospects.

Active Publication Date: 2015-12-16
四川明峰洋生物科技有限公司
View PDF3 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, so far, there are no relevant reports on the bactericidal activity of this compound against agricultural fungi and bacterial diseases

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 isoflavonoids compound to prepare agricultural bactericide
  • Application of isoflavonoids compound to prepare agricultural bactericide
  • Application of isoflavonoids compound to prepare agricultural bactericide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Antibacterial activity of glabridin of formula (I) of the present invention

[0024] Microdilution method was used to determine the effect of glabridin on R. solanacearum, R. solanacearum, E. carotovora and P. syringa epv. Actinidae 4 Antibacterial activity of the tested bacteria. All strains were provided by the Pollution-free Pesticide Research Laboratory of Sichuan Agricultural University.

[0025] Insert the bacteria to be tested into Mueller-Hinton broth medium, cultivate at 35°C for 48h, transfer to 0.9% normal saline after being slightly turbid, and adjust to a McFarland turbidity of 0.5 (the measurement method is to use a spectrophotometer to make it The absorbance at 650nm wavelength is 0.020), and then diluted 200 times with Mueller-Hinton broth medium for later use. Connect the diluted bacterial solution to a 96-well plate, add 100 μl of liquid to each well, and then add 100 μl of the drug solution to be tested at different concentrations prepared by steril...

Embodiment 2

[0030] The spore germination inhibition method was used to determine the effect of glabridin on Botrytis cinerea, Fusarium graminearum, Phytophthora infestans, Pyricularia grisea and Colletotrichum gloeosporioides, etc. Antibacterial activity of the tested fungi. All strains were provided by the Pollution-free Pesticide Research Laboratory of Sichuan Agricultural University.

[0031] Inhibition of spore germination method: the spores of pathogenic fungi are made into a spore suspension of a certain concentration (under a 10×10 low-magnification lens, there are 20 to 40 spores per field of view), and different concentrations of glabridin are mixed with the spore suspension. After mixing, the droplets were added onto the concave glass slide, and each treatment was repeated 3 times. Carbendazim was used as the drug control, and sterile water was used as the blank control. After cultivating in moisture at 25°C for 8h to 12h, check the germination of the control spores. After the...

Embodiment 3

[0036] The combined effect of embodiment triglabridin and levoshikonin on pathogenic fungi

[0037] 1.1 Inhibitory toxicity of glabridin and levoshikonin to pathogenic fungi

[0038] The toxicity of glabridin and levoshikonin to wheat scab and tea anthracnose was measured with reference to the method in Example 2.

[0039] 1.2 Research on compounding effect of two compounds

[0040] Composite glabridin and levoshikonin: the two compounds are formulated into 5 ratios (mass ratio) of 3:1, 2:1, 1:1, 1:2, and 1:3 according to the mass ratio . The above formulations were tested for toxicity according to the drug toxicity test method.

[0041] To evaluate the combined effect of the mixture, the EC 50 Based on the value, the joint effect type of the mixture was evaluated by calculating the co-toxicity coefficient of the mixture.

[0042]

[0043] CTC≥120 is a synergistic effect, 80≤CTC<120 is an additive effect, and CTC<80 is an antagonistic effect.

[0044] 1.3 Test results ...

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 relates to an application of an isoflavonoids compound, that is, glabridin, to prepare an agricultural bactericide. The compound is used for inhibiting the following pathogenic funguses of crops: fusarium graminearum, colletotrichum gloeosporioides, botrytis cinerea, phytophthora infestans, or pyricularia grisea, and the following pathogenic bacteria of crops: erwina carotovora, pseudomonas solanacearum, ralstonia solanacearum, or pseudomonas syringae pv. actinidae. Furthermore, the compound can be prepared into various formulations with other agricultural auxiliaries, and the compound has a synergistic effect after combined with shikonin according to a certain weight ratio.

Description

technical field [0001] The invention belongs to the field of agricultural fungicides, and in particular relates to the use of glabridin in preparing agricultural fungicides. technical background [0002] Glabridin belongs to isoflavones and is mainly isolated from Glycyrrhiza glabra. At present, the use of glabridin is mainly concentrated in the field of medicine, and it has shown great applications in anti-oxidation, anti-inflammation, anti-atherosclerosis, lowering blood fat, lowering blood pressure, neuroprotection, enhancing memory, and anti-obesity. Among them, anti-oxidation and anti-inflammatory effects are more researched. For example, Vaya (1997) found that glabridin can inhibit the consumption of β-carotene, and at the same time affect the formation of CLOOH and the consumption of CL in the oxidation reaction of LDL induced by AAPH. Kent (2002) et al found that glabridin exhibited significant anti-free radical oxidation in the oxidation system of cytochrome P450 / ...

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): A01N43/90A01P3/00A01P1/00
Inventor 杨春平陈华保钱勇张敏龚国淑常小丽蒋春先王海建李沛利邱小燕田悦
Owner 四川明峰洋生物科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com