Fibroblast cell growth factor receptor selective inhibitor

By developing a new compound of formula (I) as a selective inhibitor of FGFR4, the problem of insufficient selectivity of FGFR4 inhibitors in the existing technology has been solved, effective inhibition of FGFR4 has been achieved, and the therapeutic effect of various cancers has been significantly improved.

CN107286108AInactive Publication Date: 2017-10-24CHENGDU RONGKE BOHAI TECH CO LTD
0 Cites 0 Cited by

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2016-07-21
Publication Date
2017-10-24
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

Existing FGFR4 inhibitors have insufficient selectivity and stability issues in the treatment of various cancers, and are difficult to effectively inhibit the interaction between FGF19 and FGFR4, resulting in poor therapeutic effects.

Method used

A new type of compound of formula (I) and its salts were developed as a selective inhibitor of FGFR4. Through specific structural design and synthesis methods, the inhibitory effect on FGFR4 was improved, and used in drug combinations to enhance the therapeutic effect.

Benefits of technology

The compound significantly inhibits the kinase activity of FGFR4 with high selectivity and significant inhibitory effect on FGFR4. It is used to treat various cancers such as liver cancer, gastric cancer, renal cell carcinoma, etc., improving the pertinence and effect of the treatment.

✦ Generated by Eureka AI based on patent content.
Patent Text Reader

Abstract

The invention relates to a fibroblast cell growth factor receptor selective inhibitor and provides a compound expressed by a formula (I), stereoisomers, tautomers or pharmacologically acceptable salts thereof, and application of the compound used as an FGFR4 kinase selective inhibitor and used for preparing medicines or medicine compositions for treating diseases caused by FGFR4 or FGF19. The compound has selective obvious inhibition activity on FGFR4 and has a broad application prospect in the field of tumor treatment. The formula (I) is shown in the description.
Need to check novelty before this filing date? Find Prior Art