Application of 2 alpha-hydroxy protopanoxadiol medicine

A panaxadiol and drug technology, which is applied to the application field of 2α-hydroxy protopanaxadiol in the preparation of antitumor drugs, can solve few problems and the like, and achieve the effects of inhibiting proliferation and inhibiting tumor significantly.

Inactive Publication Date: 2012-04-04
FUDAN UNIV
View PDF0 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are few studies and reports on the function of 2α-hydroxyprotopanaxadiol, especially the clear medicinal function

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 2 alpha-hydroxy protopanoxadiol medicine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Example 1 Determination of the inhibitory effect of 2α-hydroxyprotopanaxadiol on the growth of pancreatic cancer cells by MTS method

[0035] 3000 PANC-1 cells (purchased from the Chinese Academy of Sciences Cell Bank) were inoculated into 96-well plates, cultured for 24 hours to allow them to adhere to the wall, and then 2α-hydroxyprotopanaxadiol (purchased from the Shanghai Institute of Materia Medica, Chinese Academy of Sciences) was added. 6 concentration gradients, with 3 replicate wells for each concentration. Cells at 37°C, 5% CO 2 After culturing for 72 hours under the same conditions, the culture medium was discarded, and the cell viability was measured with an MTS kit (Promega).

[0036] The test method is: wash the cells once with serum-free medium, and add the pre-prepared MTS chromogenic solution according to the amount of 100 μl / well (add 2ml of solution 1 and 100μl of solution 2 to 10ml of serum-free medium, and mix well). A well without cells was set a...

Embodiment 2

[0039] Example 2 Growth inhibitory effect of 2α-hydroxyprotopanaxadiol on human leukemia cells

[0040] Using cck-8 kit (Japan Dojin Chemical Research Institute) detection.

[0041] steps:

[0042] 1) K562 cells (purchased from ATCC) were evenly seeded in a 96-well plate, with 10,000 cells per well.

[0043] 2) Leave to adhere to the wall, add drugs after overnight, add drugs (2α-hydroxyprotopanaxadiol concentrations are 50, 16.67, 5.56, 1.85, 0.62 μM, and each concentration has 3 replicate wells.

[0044] 3) After culturing for 48 hours, replace the complete medium with a mixture of serum-free medium and CCK8 (10:1), and incubate in a 37°C incubator for 2 hours.

[0045] 4) Take 450nm as the measurement wavelength and 650nm as the reference wavelength, and measure the reading on a microplate reader.

[0046] Results: The IC50 value of 2α-hydroxyprotopanaxadiol on k562 cells was 4.77μM.

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 belongs to the fields of chemical industries and medicines, and relates to the application of 2 alpha-hydroxy protopanoxadiol in preparation of antitumor medicines. Antitumor cells comprise leukemia or pancreatic cancers. The 2 alpha-hydroxy protopanoxadiol belongs to a natural product and has certain clinical application value. A small molecular compound is used as a new antitumor medicine or an auxiliary component of the new antitumor medicine for development, has an obvious antitumor effect, is environment-friendly and provides a new method for treating and healing tumors.

Description

technical field [0001] The invention belongs to the fields of chemical industry and medicine, and relates to the application of 2α-hydroxy protopanaxadiol in the preparation of antitumor drugs. Background technique [0002] 2α-Hydroxy protopanaxadiol has the following structural formula. [0003] [0004] 1999 [0005] In 1998, Cui Jian-Fang et al prepared 2α-hydroxy protopanaxadiol (compound 6 in Table 1, Alkaline cleavage of gypenosides and characterization of dammarane-type aglycons by gas chromatography-mass spectrometry.Phytochemical Analysis. 9(3), 128-133). In 1999, Cui et al. reported a method for separating and identifying 2α-hydroxyl protopanaxadiol from Gynostemma pentaphyllum (compound 7, Gynostemma pentaphyllum: identification of major sapogenins and differentiation from Panax species. European Journal of Pharmaceutical Sciences.8(3), 187-191). However, there are few studies and reports on the function of 2α-hydroxyprotopanaxadiol, especially the clear me...

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): A61K31/575A61P35/00A61P35/02C12Q1/02
Inventor 余龙唐丽莎刘祖龙胡立宏
Owner FUDAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products