血小板源性生长因子受体
生长因子受体
受体酪氨酸激酶
酪氨酸激酶
药物发现
癌症研究
血小板衍生生长因子
药品
受体
计算生物学
生长因子
生物
药理学
生物信息学
生物化学
作者
Hailong Zhang,Qian Kong
标识
DOI:10.4155/ppa-2023-0005
摘要
Type III receptor tyrosine kinase, e.g., PDGFR, are associated with various autoimmune diseases. To show the status of PDGFR and c-KIT targets, we performed the US patent analysis. The present study showed that the R&D of c-KIT target was much earlier than the R&D of PDGFR targets. Currently, the PDGFR-based target demonstrates more applications in the development of biological therapy. Our findings indicated that some inhibitors of c-KIT target contained sulfur elements or 1,3-diazine rings. The c-KIT target has more competitive edges for chemical drug discovery than the PDGFR target. c-KIT and PDGFR targets are currently preferable for drug discovery in autoimmune diseases. This study was the first to show R&D differentiation between PDGFR and c-KIT targets in drug development.
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