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

Application of Pityriacitrin alkaloid and derivative thereof in resisting plant viruses and pathogenic bacteria

A technology of anti-plant virus and anti-plant virus agent, applied in botany equipment and methods, chemicals for biological control, applications, etc., can solve the problem of low synthesis yield, high cost, low natural content of pityriacitrins alkaloids, etc. Problems, to achieve the effect of expanding the scope of application, good anti-plant virus and bacteria activity

Active Publication Date: 2021-08-24
HEBEI UNIV OF TECH
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] Through literature research, due to the low natural content of pityriacitrins alkaloids, low synthesis yield and high cost, researchers mainly focus on the application of pityriacitrins in medicine, especially anti-tumor, and there are few reports on the control of diseases and insect pests.

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 Pityriacitrin alkaloid and derivative thereof in resisting plant viruses and pathogenic bacteria
  • Application of Pityriacitrin alkaloid and derivative thereof in resisting plant viruses and pathogenic bacteria
  • Application of Pityriacitrin alkaloid and derivative thereof in resisting plant viruses and pathogenic bacteria

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] The pityriacitrin alkaloids and their derivatives represented by the following 1 to 20 chemical structural formulas of the present invention are obtained by referring to existing literature (Chem.Eur.J.2013,19,10132-10137; RSC Adv.,2014,4,26258- 26263.) prepared by the method disclosed,

[0016]

[0017] in,

[0018] The compound shown in chemical structure formula 1 is pityriacitrin alkaloid,

[0019] The pityriacitrin derivative shown in chemical structural formula 2 is phenyl (9H-pyrido [3,4-b] indol-1-yl) ketone,

[0020] The pityriacitrin derivative shown in chemical structure 3 is (2-chlorophenyl) (9H-pyrido [3,4-b] indol-1-yl) ketone,

[0021] The pityriacitrin derivative shown in chemical structure 4 is (2-bromophenyl) (9H-pyrido [3,4-b] indol-1-yl) ketone,

[0022] The pityriacitrin B derivative shown in chemical structural formula 5 is 1-(1H-indole-3-carbonyl)-9H-pyrido[3,4-b]indole-3-carboxylic acid methyl ester,

[0023] Chemical structural formula 6 ...

Embodiment 2

[0039] The individual compounds of pityriacitrin alkaloids and derivatives thereof shown in the above 1 to 20 chemical structural formulas are used as anti-plant virus agents:

[0040] The measurement of the anti-tobacco mosaic virus activity of the individual compounds of pityriacitrin alkaloids and derivatives thereof shown in the above 1 to 20 chemical structural formulas, the measurement procedure is as follows:

[0041] The first step, tobacco mosaic virus purification and concentration determination:

[0042] Tobacco mosaic virus purification and concentration determination were carried out in accordance with the Tobacco Mosaic Virus SOP specification compiled by the Bioassay Laboratory of the Institute of Elements, Nankai University. After the virus crude extract was centrifuged twice with polyethylene glycol, the measured concentration was 20 μg / mL, and refrigerated at 4 °C spare;

[0043] In the second step, preparation of individual compound medicament solutions of ...

Embodiment 3

[0060] The individual compounds of pityriacitrin alkaloids and derivatives thereof shown in the above 1 to 20 chemical structural formulas are used as phytopathogenic fungicides,

[0061] A. In vitro bactericidal test, bacterial growth rate determination method (plate method):

[0062] The antibacterial activity test of the individual compounds of pityriacitrin alkaloids and derivatives thereof shown in the above 1 to 20 chemical structural formulas, in vitro bactericidal test, the determination procedure is as follows:

[0063] Determination of bacterial growth rate is the plate method: respectively dissolve 3 mg of the individual compounds of pityriacitrin alkaloids and their derivatives shown in the above 1 to 20 chemical structural formulas in 0.03 mL of acetone, and then use 200 μg / mL Tween 80 Dilute the aqueous solution to a test concentration of 50mg / kg, then draw 1mL of the drug solution and inject it into the corresponding Petri dish, then add 9mL of the medium, shake...

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 application of a pityriacitrin alkaloid and a derivative thereof in resisting plant viruses and pathogenic bacteria, and relates to a biocide of the pityriacitrin alkaloid containing a 1-acyl substituted beta-carboline skeleton and the derivative thereof, in particular to twenty pityriacitrin alkaloids and derivatives thereof which are used as a plant virus resisting agent and a plant pathogenic fungus killing agent, the application as the plant virus resisting agent means use for tobacco mosaic virus, pepper virus, rice virus, tomato virus, sweet potato virus, potato virus, melon virus and maize dwarf mosaic virus, and the application as the plant pathogenic fungus killing agent means use for inhibiting 15 plant pathogenic bacteria such as cucumber fusarium wilt, rice blast, peanut brown spot, apple ring rot, wheat sheath blight, corn Bipolaris maydis, watermelon anthracnose, rice malignant seedling, tomato early blight, wheat gibberella, potato late blight, phytophthora capsici, sclerotium of rape, cucumber botrytis cinerea and rice sheath blight.

Description

technical field [0001] The technical scheme of the present invention relates to the biocides of pityriacitrin alkaloids and derivatives thereof containing 1-acyl substituted β-carboline skeletons, specifically the application of pityriacitrin alkaloids and derivatives thereof in anti-plant viruses and germs. Background technique [0002] Pityriacitrins alkaloids are a class of β-carboline alkaloids with a novel structure, in which an indole structure is linked at the C-1 position of β-carboline through a carbonyl functional group. Compounds containing such core skeletons extracted from nature include pityriacitrin, pityriacitrin B, hytiosulawesine, 7-MeO-pityriacitrin, 7,2’-(MeO) 2 - pityriacitrin and 2'-MeO-6'-OH-pityriacitrin and other pityriacitrins alkaloids (Mini. Rev. Med. Chem., 2021, 21, 233-244.), as shown in structural formula 1. [0003] [0004] Since the Japanese research team first reported the isolation of pityriacitrins alkaloids from the marine bacterium...

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): A01N43/90A01P1/00A01P3/00C07D471/04
CPCA01N43/90C07D471/04
Inventor 卢爱党李林王铁男师利周雅楠苑文英
Owner HEBEI UNIV OF TECH
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