血小板生长因子受体和c-KIT靶点的专利前景。

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Pharmaceutical patent analyst Pub Date : 2023-07-01 Epub Date: 2023-09-27 DOI:10.4155/ppa-2023-0005
Hai-Long Zhang, Qian Kong
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引用次数: 0

摘要

III型受体酪氨酸激酶,例如PDGFR,与各种自身免疫性疾病有关。为了显示PDGFR和c-KIT靶点的状态,我们进行了美国专利分析。本研究表明,c-KIT靶点的研发远早于PDGFR靶点的开发。目前,基于PDGFR的靶点在生物治疗的发展中有更多的应用。我们的研究结果表明,一些c-KIT靶向抑制剂含有硫元素或1,3-二嗪环。c-KIT靶点在化学药物发现方面比PDGFR靶点更有竞争力。c-KIT和PDGFR靶点目前优选用于自身免疫性疾病中的药物发现。这项研究首次表明PDGFR和c-KIT靶点在药物开发中的研发差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patent landscape of platelet growth factor receptor and c-KIT targets.

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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来源期刊
Pharmaceutical patent analyst
Pharmaceutical patent analyst PHARMACOLOGY & PHARMACY-
CiteScore
1.80
自引率
0.00%
发文量
22
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