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

Application of composition containing heterocyclic compound in preparation of drug for treating leukemia

A compound, leukemia technology, applied in the field of medicine, can solve the problem that the activity needs to be further improved

Inactive Publication Date: 2020-06-26
黄泳华
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The phenylcarbamoylthiazole compound II with the structure shown below is also a CML drug approved by the FDA. Research by Cai Zhiping et al. Ⅱ The IC50 of K562 cells is about 244.00μg / mL, and its activity needs to be further improved

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 composition containing heterocyclic compound in preparation of drug for treating leukemia
  • Application of composition containing heterocyclic compound in preparation of drug for treating leukemia
  • Application of composition containing heterocyclic compound in preparation of drug for treating leukemia

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0079] Embodiment 1 Oral solid preparation containing pyridyl pyrimidine amine compound and its preparation method

[0080] prescription

[0081]

[0082]

[0083]

[0084]

[0085]

[0086]

[0087]

[0088] Preparation

[0089] Take the prescribed amount of MIX (X-Y) and auxiliary materials, and pass through a 100-mesh sieve. Get MIX (X-Y), lactose, microcrystalline cellulose, crospovidone and starch and fully mix; get the prescription amount of hypromellose, and prepare a solution with a concentration of 10% based on hypromellose, Use lactic acid to adjust the pH to 3.0-4.0, add it to the above-mentioned mixture to make a soft material, granulate with a 16-mesh sieve, and dry at 80°C for 3-4 hours. Use a 16-mesh sieve to sieve the granules, add the prescribed amount of micropowder silica gel and magnesium stearate, mix well, fill the capsules, and each capsule weighs about 500mg;

[0090] Take the prescribed amount of MIX (X-Y) and auxiliary mater...

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 composition containing a heterocyclic compound in preparation of a drug for treating leukemia. On one hand, the invention provides an application of composition containing pyridyl pyrilamine compounds in preparation of the drug for treating the leukemia; on the other hand, the invention provides an application of composition containing phenyl aminoformylthiazole compounds in preparation of the drug for treating the leukemia; and the invention provides an application of quinoline compounds in preparation of the drug for treating the leukemia.

Description

technical field [0001] The invention belongs to the technical field of medicine, and in particular relates to the use of a composition containing a heterocyclic compound in the preparation of a medicine for treating leukemia. Background technique [0002] The pyridyl pyrimidine amine compound I with the structure shown below is a commonly used clinical drug for treating chronic myeloid leukemia (CML), but its medicinal dose is relatively high (100mg-400mg), indicating that its anti-inflammatory effect needs to be further improved. . For example, the research results of Zhong Jihua et al. (Diagnostics Theory and Practice, 2010, 9(05): 469-472.), imatinib acts on the IC of K562, K562 / pc and K562 / CYP3A5 cells 50 The values ​​were (55.313±0.248), (57.043±0.486) and (72.910±0.776) μg / mL, respectively. [0003] [0004] The phenylcarbamoylthiazole compound II with the structure shown below is also a CML drug approved by the FDA. Research by Cai Zhiping et al. The IC50 of II ...

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): A61K31/506A61K31/426A61K31/529A61K31/496A61K31/47A61P35/02
CPCA61K31/426A61K31/47A61K31/496A61K31/506A61K31/529A61P35/02A61K2300/00
Inventor 向飞吴洁
Owner 黄泳华
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