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

Use of Icetaxane type abietane diterpene in preparing medicine for treating colorectal cancer

A technology of abietane diterpene and colorectal cancer, applied in the field of application in the preparation of colorectal cancer treatment drugs

Active Publication Date: 2021-04-09
CENT SOUTH UNIV
View PDF3 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] At present, the application of Icetexane-type abietane diterpenes in the field of antitumor only focuses on its cytotoxic activity, and there is no report on its mechanism of action

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
  • Use of Icetaxane type abietane diterpene in preparing medicine for treating colorectal cancer
  • Use of Icetaxane type abietane diterpene in preparing medicine for treating colorectal cancer
  • Use of Icetaxane type abietane diterpene in preparing medicine for treating colorectal cancer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0061] Embodiment 1 of the present invention is: the preparation method of Icetexane type abietane diterpene and its derivatives, comprising the following steps:

[0062] S1, the preparation of compound 2:

[0063]

[0064] Weigh 1.0g (3mmol) of compound 1 (carnosic acid) into a 100mL round bottom flask, add 12.5mL of toluene and 2.5mL of methanol to dissolve, slowly add 3mL of trimethylsilyldiazomethane in n-hexane dropwise at 0°C solution (2.0mol / L, 6mmol). TLC monitoring, after the reaction is complete, add 1 mL of glacial acetic acid dropwise to the reaction solution, remove the reaction solvent by rotary evaporation, add 50 mL of saturated brine, extract with ethyl acetate (3 × 30 mL), and dry the ethyl acetate layer with anhydrous sodium sulfate. Silica gel column chromatography (volume ratio of PE (petroleum ether) to EA (ethyl acrylate) was 10:1) obtained 945 mg of intermediate (yellow solid, yield 91%).

[0065] 1 H NMR (400MHz, CDCl 3 )δ7.52(s,1H),6.59(s,1H),5...

Embodiment 5

[0120] Embodiment 5 of the present invention is: flow cytometry determination (+)-Grandione influence on HCT-116 cell BiP protein translocation

[0121] HCT116 cells in the logarithmic growth phase were digested with 0.25% trypsin and blown into single cells, 5*10 cells per well 5 Cells were seeded in 6-well plates and cultured overnight in an oven. Add 20 μM, 10 μM, 5 μM, 0 μM (blank control) (+)-Grandione respectively, and incubate for 24 hours. Cells were collected, centrifuged at 1000 rpm at 4°C for 10 min, and the supernatant was discarded. Wash the cells three times with cold PBS, add 200 μL of binding buffer working solution (1×Annexin V binding buffer) to resuspend the cells, add 10 μL of Annex in V-FITC to the cell suspension, mix gently, and react at room temperature in the dark for 15 minute. Add 300 μL of binding buffer and 5 μL of PI (propidium iodide), and detect with a flow cytometer.

Embodiment 6

[0122] Embodiment 6 of the present invention is: the influence of (+)-Grandione on HCT-116 cell BiP protein translocation is determined by immunofluorescence method

[0123] HCT116 cells in the logarithmic growth phase were digested with 0.25% trypsin and blown into single cells, 5*10 cells per well 5 Cells were seeded in a 6-well plate (including cell slides), cultured overnight in an oven to adhere to the wall, and 20 μM, 10 μM, 5 μM and 0 μM (blank control) (+)-Grandione were added and incubated for 24 h. After washing with PBS for 3 times, fix with fixative solution (PBS solution with mass fraction of 4% paraformaldehyde) at 4°C for 12h, then wash with PBS for 3 times, and permeabilize with Triton-X100 (Triton) in PBS solution for 10min Finally, wash with PBS 3 times, 5% BSA in PBS solution blocked for 60min, add BiP antibody, wet box 4 overnight. The next day, wash 3 times with PBS, 5min each time, then add AlexaFluor 488goat anti-rabbit IgG secondary antibody, incubate ...

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 use of Icetaxane type abietane diterpenes in preparing a medicine for treating colorectal cancer. An action mechanism of the Icetaxane type abietane diterpenes is as follows: a level of chaperonin binding immunoglobulin protein (BiP) in endoplasmic reticulum is up-regulated, a transfer of the BiP from cytoplasm to nuclei is promoted, and cell apoptosis is further induced. The invention further expands a use range of the Icetaxane type abietane diterpene and derivatives thereof.

Description

technical field [0001] The invention relates to the technical field of medicines, in particular to the application of an Icetexane type abietane diterpene in the preparation of medicines for treating colorectal cancer. Background technique [0002] Icetexane-type abietane diterpenoids are B-ring-expanded abietane diterpenoids. There are more than 70 natural products of this type that have been reported so far. They are widely distributed and found in many families of plants. [0003] The dimeric Icetexane-type abietane diterpene biperovskatone and the Icetexane-type C18 norabietane diterpene Norperovskatone isolated from the plants of the genus Aphrodisiac possess anti-HBV activity. A dimer of C23 terpenoids and Icetexane diterpenoids isolated from Salvia gansifolia, gancy sagerenone A has the effect on a variety of tumor cell lines HL-60, SMMC-7721, A-549, MCF -7, SW480, Beas-2B have significant cytotoxic activity. Dimeric Icetexane type diterpene Premnalatifolin A has si...

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): A61K31/192A61K31/05A61K31/122A61K31/336A61K31/343A61K31/357A61P1/00A61P35/00
CPCA61K31/192A61K31/05A61K31/122A61K31/336A61K31/343A61K31/357A61P1/00A61P35/00
Inventor 邓旭周应军曹伟刘婷婷杨舒婷曾光尧
Owner CENT SOUTH 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