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

Application of Indole-3-Carboxaldehyde and Its Derivatives in Controlling Plant Diseases Caused by Phytopathogenic Fungi

A technology for phytopathogenic fungi and plant diseases, applied in the direction of chemicals, applications, biocides for biological control, etc., to ensure high quality, broad research and market application prospects, and growth inhibition effects

Active Publication Date: 2021-04-23
SOUTH CHINA AGRI UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] At present, there is no report that indole-3-carboxaldehyde has an inhibitory effect on plant pathogenic fungi at home and abroad.

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 Indole-3-Carboxaldehyde and Its Derivatives in Controlling Plant Diseases Caused by Phytopathogenic Fungi
  • Application of Indole-3-Carboxaldehyde and Its Derivatives in Controlling Plant Diseases Caused by Phytopathogenic Fungi
  • Application of Indole-3-Carboxaldehyde and Its Derivatives in Controlling Plant Diseases Caused by Phytopathogenic Fungi

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0064] Example 1 Extraction of Pseudomonas ST4 metabolites and detection of its biological activity

[0065] 1. Extraction of strain ST4 metabolites

[0066] (1) Inoculate the overnight cultured ST4 bacterial solution on a PDA plate (13×13 cm), culture at 28°C for 48 hours, and wipe off the colonies with sterile gauze to obtain a fermentation medium;

[0067] (2) Cut the fermentation medium into small pieces and soak in 3 times the volume of a mixed solution composed of ethyl acetate:methanol:glacial acetic acid at a volume ratio of 80:15:5, shake for 2 hours, and filter to collect the supernatant; Use a rotary evaporator to remove organic solvents such as ethyl acetate and methanol in the supernatant, leaving the aqueous phase solution;

[0068] (3) Extract the aqueous phase solution 3 times with 3 times the volume of ethyl acetate, collect the aqueous phase and the organic phase respectively, evaporate the organic phase to dryness using a rotary evaporator, and concentrate ...

Embodiment 2

[0075] The separation and purification of the effective active substance of embodiment 2 Pseudomonas ST4

[0076] 1. Separation and purification method

[0077] The ethyl acetate extract obtained in Example 1 was sequentially separated by Claricep FlashSilica (CS) standard silica gel column chromatography, Butch medium pressure separator, high performance liquid chromatography and HPLC semi-preparative separation, the specific methods are as follows:

[0078] (1) Standard silica gel column chromatography separation:

[0079]1) Sample loading: Accurately weigh 5-6 g of the ethyl acetate extract of Pseudomonas ST4 each time, dissolve it with an appropriate amount of methanol, add twice the amount of 60-100 mesh silica gel, stir well, and air-dry the methanol. The silica gel containing the sample is added to the sample column, connected with the Claricep FlashSilica (CS) standard silica gel column, and connected with the Butch medium pressure separator and analytical grade metha...

Embodiment 3

[0098] Molecular formula and structure identification of embodiment 3 compound ST4-2-8

[0099] 1. Structural identification: ST4-2-8 obtained in Example 2 was analyzed by NMR and LC-MS to identify its chemical structure.

[0100] 2. Identification results:

[0101] The NMR analysis of ST4-2-8 shows that the compound contains 9 carbons, 7 Hs, 1 N and 1 O atom, and contains a parallel structure of a benzene ring and a pyrrole ring, at the 3rd position of benzopyrrole Containing an aldehyde group, the possible structure is indole-3-carbaldehyde; LC-MS analyzes the molecular weight of this substance to be 146.15, consistent with indole-3-carbaldehyde; Shown by HPLC analysis with finished product ( image 3 ), the retention time of ST4-2-8 and indole-3-carbaldehyde is 8.255min, and the peak shape and three-dimensional structure are completely consistent. Therefore, ST4-2-8 is identified as indole-3-carbaldehyde.

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 discloses the application of indole-3-formaldehyde and its derivatives in preventing and treating plant diseases caused by plant pathogenic fungi. The invention provides the application of indole-3-carboxaldehyde or its derivatives or pharmaceutically acceptable salts in the prevention and treatment of plant diseases caused by phytopathogenic fungi, or in the preparation of pesticides for the prevention and control of plant diseases caused by phytopathogenic fungi Or application in biocontrol agents. The present invention proves that indole-3-formaldehyde and derivatives thereof have good inhibitory activity to phytopathogenic fungi through the measurement of bacteriostatic activity, and it has a good inhibitory effect on the growth and sexual coordination of phytopathogenic fungi, which can inhibit The formation of dikaryotic mycelia prevents phytopathogenic fungi from normally infecting plants, thereby effectively inhibiting the occurrence of plant fungal diseases, providing a reference for green prevention and control of plant diseases caused by phytopathogenic fungi, and has broad application prospects.

Description

technical field [0001] The invention belongs to the technical field of biological control. More specifically, it relates to the application of indole-3-carbaldehyde and its derivatives in the control of plant diseases caused by phytopathogenic fungi. Background technique [0002] Indole-3-carboxaldehyde is an important pharmaceutical intermediate, mainly used in the preparation of indole derivatives. Indole compounds are an important class of heterocyclic compounds with a wide range of biological activities. Indole secondary metabolites widely exist in cruciferous vegetables and a large number of marine organisms and actinomycetes. In recent years, its anticancer activity has attracted widespread attention. Currently, SU11248 (trade name: sunitinib), vinblastine (VLB, Vinblastine), vincristine (VCR, Vincristine), vindesine (VDS, Vindesine), vinorelbine (VBR, Vinorelbine), indirubin A small amount of varieties containing indole structures such as red have been put into us...

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 Patents(China)
IPC IPC(8): A01N43/38A01P3/00
CPCA01N43/38
Inventor 张炼辉刘诗胤周佳暖贺飞林诺翘
Owner SOUTH CHINA AGRI UNIV
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