Department of Medical Chemistry, X-Chem, Montreal, Québec, Canada.
Computational Chemistry Consulting Services, Jaén, Spain.
Expert Opin Ther Pat. 2024 Oct;34(10):843-861. doi: 10.1080/13543776.2024.2400175. Epub 2024 Sep 11.
Covalent drugs contain electrophilic groups that can react with nucleophilic amino acids located in the active sites of proteins, particularly enzymes. Recently, there has been considerable interest in using covalent drugs to target non-catalytic amino acids in proteins to modulate difficult targets (i.e. targeted covalent inhibitors). Covalent compounds contain a wide variety of covalent reacting groups (CRGs), but only a few of these CRGs are present in FDA-approved covalent drugs.
This review summarizes a 2020-23 patent landscape analysis that examined trends in the field of covalent drug discovery around targets and organizations. The analysis focused on patent applications that were submitted to the World International Patent Organization and selected using a combination of keywords and structural searches based on CRGs present in FDA-approved drugs.
A total of 707 patent applications from >300 organizations were identified, disclosing compounds that acted at 71 targets. Patent application counts for five targets accounted for ~63% of the total counts (i.e. BTK, EGFR, FGFR, KRAS, and SARS-CoV-2 Mpro). The organization with the largest number of patent counts was an academic institution (Dana-Farber Cancer Institute). For one target, KRAS G12C, the discovery of new drugs was highly competitive (>100 organizations, 186 patent applications).
共价药物含有亲电基团,可与蛋白质(尤其是酶)活性部位的亲核氨基酸发生反应。最近,人们对使用共价药物靶向蛋白质中非催化氨基酸以调节难靶标(即靶向共价抑制剂)产生了浓厚的兴趣。共价化合物包含多种共价反应基团(CRG),但在 FDA 批准的共价药物中,只有少数几种 CRG 存在。
本综述总结了 2020 年至 2023 年的专利景观分析,该分析检查了围绕目标和组织的共价药物发现领域的趋势。该分析侧重于向世界国际专利组织提交的专利申请,并使用基于 FDA 批准药物中存在的 CRG 的关键词和结构搜索的组合进行选择。
共确定了来自 300 多个组织的 707 项专利申请,披露了作用于 71 个靶标的化合物。五个靶标专利申请的数量约占总数量的 63%(即 BTK、EGFR、FGFR、KRAS 和 SARS-CoV-2 Mpro)。专利申请数量最多的组织是一家学术机构(Dana-Farber 癌症研究所)。对于一个靶标 KRAS G12C,新药的发现竞争非常激烈(>100 个组织,186 项专利申请)。