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

Application of diindoloquinazoline alkaloid in preparation of antitumor drugs and antifungal drugs

A technology of bisindolequinazoline and indolequinazoline, which can be applied in the directions of antitumor drugs, antifungal agents, drug combinations, etc., can solve the problems of high toxicity or irritation, etc.

Active Publication Date: 2012-04-04
INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI
View PDF2 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Most of the antifungal drugs currently used in clinical practice are synthetic, which have the disadvantages of toxicity or irritation to varying degrees. Therefore, people have turned their attention to natural products.

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 diindoloquinazoline alkaloid in preparation of antitumor drugs and antifungal drugs
  • Application of diindoloquinazoline alkaloid in preparation of antitumor drugs and antifungal drugs
  • Application of diindoloquinazoline alkaloid in preparation of antitumor drugs and antifungal drugs

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Example 1. Isolation and identification of compound I from raw Evodia rutaecarpa

[0030] Raw Evodia rutaecarpa 4Kg, first take out 200g and use a volatile oil extractor to extract about 2ml of Evodia rutaecarpa volatile oil, and prepare it for GC-MS. The dregs and the remaining raw Evodia rutaecarpa were combined and extracted 3 times with 80% ethanol under reflux, each time for 3 hours, the alcohol extract was combined, concentrated under reduced pressure to obtain about 800 g of thick extract, dissolved in water to a suspension, and successively washed with petroleum ether (60 -90°C), chloroform, ethyl acetate and water-saturated n-butanol were extracted, concentrated into extract respectively to obtain petroleum ether fraction 14g, chloroform fraction 209g, ethyl acetate fraction 26g, n-butanol fraction 210g, and water fraction 316g. The chloroform part was repeatedly passed through silica gel normal pressure (LC), low pressure (LPLC) and medium pressure column chro...

Embodiment 2

[0043] Example 2. Isolation and Identification of Compound I from Glycyrrhizae Evodiaecarpa

[0044] Evodia rutaecarpa 9.5Kg was prepared from sugar, cold soaked in petroleum ether for 7 days to obtain 67g of petroleum ether extract; the dregs after degreasing were reflux extracted with 80% ethanol for 3 times, each time for 3 hours, combined with alcohol extracts, concentrated under reduced pressure to obtain The thick extract is about 1.5Kg; add 2% acid water and knead to dissolve to the suspension, and extract the acid water with ethyl acetate to obtain 263g of ethyl acetate extract; the extracted acid water is alkalized to pH 9-10 by adding ammonia water , extracted with chloroform to obtain 126g of chloroform extract with more concentrated total alkaloids; finally the alkaline water was adjusted to neutral and extracted with n-butanol to obtain 293g of n-butanol extract. The chloroform extract was repeatedly passed through silica gel normal pressure (LC), low pressure (LP...

Embodiment 3

[0045] Example 3. Anti-tumor activity evaluation experiment of compound 1 by zebrafish method

[0046] 1. Research materials:

[0047] 1.1 Zebrafish embryos

[0048] 1.2 Screening Compounds

[0049] Hydroxyevodiamine, Evodiamine, Evodiamine, Evodiamide I, Evodiamine

[0050] 2. Experimental method

[0051] 2.1 Zebrafish model

[0052] 2.1.1 Model Basis

[0053] The occurrence of tumor is a complex and multi-link process of transforming normal cells into cancer cells. The size of the tumor exceeds 0.2-2.0 (about 10 5 ~10 6 cells), it begins to build its own blood supply system, that is, new angiogenesis. Angiogenesis is a process in which new blood vessels grow from lateral sprouts protruding from the existing vascular system, and its main feature is the proliferation of endothelial cells (EC) lining the inside of new blood vessels. This endothelial cell proliferates extremely rapidly, far exceeding other normal tissues, and this unique phenotype of endothelial cells is...

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

PropertyMeasurementUnit
Tumor inhibition rateaaaaaaaaaa
Login to View More

Abstract

The present invention relates to a diindoloquinazoline alkaloid and diindoloquinazoline alkaloid derivatives. The structure of the diindoloquinazoline alkaloid is represented by the right formula. The diindoloquinazoline alkaloid is a dimmer compound formed by linkage of two different indoloquinazoline alkaloids with C-C bonds. The present invention further relates to a preparation method for the compounds, and antitumor activities and antifungal activities of the compounds. The diindoloquinazoline alkaloid and the diindoloquinazoline alkaloid derivatives of the present invention can be applicable for the field of medicine.

Description

1. Technical field: [0001] The invention relates to a bis-indole quinazoline alkaloid, which has the following structure, a dimer compound composed of two different indole quinazoline alkaloids connected by C-C and a preparation method. [0002] The invention belongs to medicaments, and relates to the combination with natural and synthetic bis-indole quinazoline alkaloid derivatives and their medicaments, and their application in pharmacy with antitumor and antifungal activities. 2. Technical background: [0003] Rutaceae (Rutaceae) genus Evodia has about 150 species in the world, distributed in Asia, East Africa and Oceania. There are 20 species and 5 varieties in my country, most of which are commonly used Chinese herbal medicines. As early as in "Shen Nong's Materia Medica", Evodia rutaecarpa was recorded. It has a long history of application and remarkable clinical effects. , soothe the liver, relieve depression, promote qi and relieve pain, and are quite popular among p...

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
IPC IPC(8): C07D471/14A61K31/519A61P35/00A61P31/10A61P35/02
Inventor 王奇志冯煦王鸣陈雨单宇印敏管福琴赵兴增赵友谊孙浩
Owner INST OF BOTANY JIANGSU PROVINCE & CHINESE ACADEMY OF SCI
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