Optical voidness quinazoline compound

A compound, quinazoline technology, applied in the fields of drug combination, organic chemistry, skin diseases, etc., can solve the problem of no optically pure isomer research, and achieve the effect of excellent anti-tumor activity

CN102344445AActive Publication Date: 2012-02-08JIANGSU HANSOH PHARMA CO LTD
6 Cites 0 Cited by

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Publication Date
2012-02-08
Patent Text Reader

Abstract

The invention relates to an optical voidness quinazoline compound, in particular to a compound in a general formula (I), a treatment effective dose-contained medical composite of the compound, and the application of the optical voidness quinazoline compound in preparing drugs for treating and adjusting c-erbB-2 and / or EGF-R protein tyrosine kinase activity related diseases.
Need to check novelty before this filing date? Find Prior Art

Description

technical field The invention relates to an optically pure quinazoline compound, a pharmaceutical composition containing a therapeutically effective amount of the compound, and its preparation for treating diseases related to the regulation of c-erbB-2 and / or EGF-R protein tyrosine kinase activity use in medicines. Background technique Protein tyrosine kinases catalyze the phosphorylation of specific tyrosine residues in various proteins involved in the regulation of cell growth and differentiation. Protein tyrosine kinases can be broadly classified as receptor (eg EGFr, c-erbB-2, c-met, tie-2, PDGFr, FGFr) or non-receptor (eg c-src, lck, zap70) kinases. Inappropriate or uncontrolled activation of many of these kinases, i.e. aberrant protein tyrosine kinase activity e.g. by overexpression or mutation, has been shown to lead to uncontrolled cellular production. Abnormal activities of protein tyrosine kinases, such as c-erbB-2, c-src, c-met, EGFr, PDGFr, are associated with...

Examples

preparation example 1

preparation example 2

preparation example 3