Ali Farak, Alom Shahnaz, Ali Sheikh Rezzak, Kondoli Biswanarayan, Sadhu Prativa, Borah Chinmoyee, Kakoti Bibhuti Bushan, Ghosh Surajit Kumar, Shakya Anshul, Ahmed Abdul Baquee, Singh Udaya Pratap, Bhat Hans Raj
Department of Pharmaceutical Sciences, Dibrugarh University, Dibrugarh, Assam, 786004, India.
Girijananda Chowdhury Institute of Pharmaceutical Science, Tezpur Medical College and Hospital, Tezpur, Sonitpur Assam, 784501,India.
Mini Rev Med Chem. 2024;24(12):1203-1225. doi: 10.2174/1389557523666230914103339.
Ebselen is a selenoorganic chiral compound with antioxidant properties comparable to glutathione peroxidase. It is also known as 2-phenyl-1,2-benzisoselenazol-3(2H)-one. In studies examining its numerous pharmacological activities, including antioxidant, anticancer, antiviral, and anti- Alzheimer's, ebselen has demonstrated promising results. This review's primary objective was to emphasize the numerous synthesis pathways of ebselen and their efficacy in fighting cancer. The data were collected from multiple sources, including Scopus, PubMed, Google Scholar, Web of Science, and Publons. The starting reagents for the synthesis of ebselen are 2-aminobenzoic acid and N-phenyl benzamide. It was discovered that ebselen has the ability to initiate apoptosis in malignant cells and prevent the formation of new cancer cells by scavenging free radicals. In addition, ebselen increases tumor cell susceptibility to apoptosis by inhibiting TNF-α mediated NF-kB activation. Ebselen can inhibit both doxorubicin and daunorubicin-induced cardiotoxicity. Allopurinol and ebselen administered orally can be used to suppress renal ototoxicity and nephrotoxicity. Due to excessive administration, diclofenac can induce malignancy of the gastrointestinal tract, which ebselen can effectively suppress. Recent research has demonstrated ebselen to inhibit viral function by binding to cysteinecontaining catalytic domains of various viral proteases. It was discovered that ebselen could inhibit the catalytic dyad function of M by forming an irreversible covalent bond between Se and Cys145, thereby altering protease function and inhibiting SARS-CoV-2. Ebselen may also inhibit the activation of endosomal NADPH oxidase of vascular endothelial cells, which is believed to be required for thrombotic complications in COVID-19. In this review, we have included various studies conducted on the anticancer effect of ebselen as well as its inhibition of SARS-CoV-2.
依布硒啉是一种具有抗氧化特性的有机硒手性化合物,其抗氧化性能与谷胱甘肽过氧化物酶相当。它也被称为2-苯基-1,2-苯并异硒唑-3(2H)-酮。在研究其众多药理活性(包括抗氧化、抗癌、抗病毒和抗阿尔茨海默病)时,依布硒啉已显示出有前景的结果。本综述的主要目的是强调依布硒啉的多种合成途径及其抗癌功效。数据收集自多个来源,包括Scopus、PubMed、谷歌学术、科学网和Publons。合成依布硒啉的起始试剂是2-氨基苯甲酸和N-苯基苯甲酰胺。研究发现,依布硒啉能够引发恶性细胞凋亡,并通过清除自由基来阻止新癌细胞的形成。此外,依布硒啉通过抑制肿瘤坏死因子-α介导的核因子-κB激活来增加肿瘤细胞对凋亡的敏感性。依布硒啉可以抑制阿霉素和柔红霉素诱导的心脏毒性。口服别嘌醇和依布硒啉可用于抑制肾耳毒性和肾毒性。由于过量给药,双氯芬酸可诱发胃肠道恶性肿瘤,而依布硒啉可有效抑制。最近的研究表明,依布硒啉通过与各种病毒蛋白酶的含半胱氨酸催化结构域结合来抑制病毒功能。研究发现,依布硒啉可通过在硒和半胱氨酸145之间形成不可逆的共价键来抑制M的催化二元功能,从而改变蛋白酶功能并抑制严重急性呼吸综合征冠状病毒2。依布硒啉还可能抑制血管内皮细胞内体烟酰胺腺嘌呤二核苷酸磷酸氧化酶的激活,这被认为是2019冠状病毒病血栓并发症所必需的。在本综述中,我们纳入了关于依布硒啉抗癌作用及其对严重急性呼吸综合征冠状病毒2抑制作用的各种研究。