Application of chlorsulfuron benzene ring 5-substituted derivative in preparation of antitumor drugs

A technology of chlorsulfuron benzoyl ring and anti-tumor drug, which can be applied in the direction of anti-tumor drugs, drug combinations, active ingredients of heterocyclic compounds, etc., and can solve the problems of little research on anti-tumor compounds.

Pending Publication Date: 2021-09-17
NANKAI UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are very few domestic studies on sulfonylurea anti-tumor compounds, and there are few reports

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 chlorsulfuron benzene ring 5-substituted derivative in preparation of antitumor drugs
  • Application of chlorsulfuron benzene ring 5-substituted derivative in preparation of antitumor drugs
  • Application of chlorsulfuron benzene ring 5-substituted derivative in preparation of antitumor drugs

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0015] experimental method:

[0016] Compound configuration

[0017] (1) Weigh an appropriate amount of the new compound into a 1.5mL enzyme-free sterile EP tube, and mark the name of the compound on the side wall of the EP tube. According to the relative molecular mass of the compound, calculate the volume of DMSO added to make it The final concentration was 10 mM.

[0018] (2) Use a pipette gun to add the corresponding volume of DMSO in the ultra-clean bench of the cell room, and mix evenly by pipetting, so that the compound can be completely dissolved.

[0019] (3) Heat the 1.5mL EP tube in a 95°C metal bath for 10 minutes, then divide the compound solution into small tubes for later use.

[0020] (4) Store the compound solution in a refrigerator-20.

[0021] Preparation of MTT solution

[0022] (1) Take out a 50mL centrifuge tube in the ultra-clean bench, and add 20mL of sterilized PBS into it.

[0023] (2) Open the 100mg package of MTT, suck 1mL of PBS from the 50mL ...

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 relates to an application of a chlorsulfuron benzene ring 5-substituted derivative in preparation of antitumor drugs. The general formula of the chemical structure of the chlorsulfuron benzene ring 5-substituted compound is shown in the specification, wherein R is selected from halogen, nitro, cyano, trifluoromethyl, halogenated C1-C6 alkyl, C1-C6 alkoxy, halogenated C1-C6 alkoxy, C1-C6 alkylthio, halogenated C1-C6 alkylthio, C1-C6 alkoxy carbonyl, halogenated C3-C6 cycloalkyl or N, N-(C1-C6 alkyl) carbamoyl, N, N-(C1-C6 alkyl) amino sulfonyl, N, O and S-containing ternary-five-membered heterocyclic ring is substituted by C1-C6 alkyl, N, O and S-containing ternary-five-membered heterocyclic ring and the N, O and S-containing ternary-five-membered heterocyclic ring substituted by C1-C6 alkyl. The invention discovers that the chlorsulfuron benzene ring 5-substituted derivative has an inhibition function on breast cancer cells for the first time, and can be used for preparing antitumor drugs.

Description

technical field [0001] The invention relates to the application of a class of derivatives substituted at the 5-position of chlorsulfuron benzene ring in the preparation of antitumor drugs Background technique [0002] Cancer, also known as malignant tumor, is an important disease that endangers human health. According to data released by the Ministry of Health in 2010, cancer has become an important factor in the death of Chinese people. Therefore, the treatment of cancer is particularly important. Cancer generally involves the mutation of multiple genes: when the genes that regulate cell growth are mutated or damaged, the programmed death of the cell itself is inhibited, making the cells grow out of control, continue to grow and divide, and then transform into tumors. At the same time, these tumors The process of cell infiltration and metastasis can accelerate the formation of tumor new capillaries. Although there are many antineoplastic drugs, there are few ideal drugs,...

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): A61K31/53A61P15/14A61P35/00C07D251/16C07D403/12
CPCA61K31/53A61P15/14A61P35/00C07D251/16C07D403/12
Inventor 周莎吕鑫屹武磊郭宸辰华学文周沙李正名
Owner NANKAI 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