Peng Zhenyu, Chen Leyuan, Wang Manjiang, Yue Xufan, Wei Huiqiang, Xu Feifei, Hou Wenbin, Li Yiliang
Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Institute of Radiation Medicine, Peking Union Medical College & Chinese Academy of Medical Sciences, Tianjin, China.
Expert Opin Ther Pat. 2023 Oct;33(10):669-680. doi: 10.1080/13543776.2023.2291393. Epub 2024 Jan 10.
Sterol regulatory element-binding proteins (SREBPs) are a family of membrane-binding transcription factors that activate genes encoding enzymes required for cholesterol and unsaturated fatty acid synthesis. Overactivation of SREBP is related to the occurrence and development of diabetes, nonalcoholic fatty liver, tumor, and other diseases. In the past period, many SREBP inhibitors have been found.
This manuscript is a patent review of SREBP inhibitors. We searched 2008 to date for all data from the US patent database (https://www.uspto.gov/) and the European patent database (https://www.epo.org/) with 'SREBP' and 'inhibitor' as keywords and analyzed the search results.
Both synthetic and natural SREBP inhibitors have been reported. Despite the lack of cocrystal structure of SREBP inhibitor, the mechanisms of several compounds have been clarified. Importantly, some SREBP inhibitors have been proved to have good activity in preclinical studies. As the characteristics of lipid metabolism reprogramming in cardio-cerebrovascular diseases and tumors are gradually revealed, more and more attention will be focused on SREBP.
固醇调节元件结合蛋白(SREBPs)是一类膜结合转录因子家族,可激活编码胆固醇和不饱和脂肪酸合成所需酶的基因。SREBP的过度激活与糖尿病、非酒精性脂肪肝、肿瘤等疾病的发生发展有关。在过去一段时间里,已发现许多SREBP抑制剂。
本手稿是对SREBP抑制剂的专利综述。我们以“SREBP”和“抑制剂”为关键词,检索了2008年至今美国专利数据库(https://www.uspto.gov/)和欧洲专利数据库(https://www.epo.org/)中的所有数据,并对检索结果进行了分析。
已报道了合成和天然的SREBP抑制剂。尽管缺乏SREBP抑制剂的共晶体结构,但几种化合物的作用机制已得到阐明。重要的是,一些SREBP抑制剂已在临床前研究中被证明具有良好的活性。随着心脑血管疾病和肿瘤中脂质代谢重编程特征的逐渐揭示,SREBP将受到越来越多的关注。