REVIEW ON THE SIGNIFICANCE OF PYRIMIDINE DERIVATIVES AS POTENT ANTI-ANGIOGENIC VEGFR-2 INHIBITORS

Ibrahim Issa, Abdulrahman M. Saleh, M. Khalifa, H. Mahdy
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Abstract

Cancer is a disease in which human cells grow uncontrollably and spread to other body parts. Cancer is the second leading cause of death globally and accounted for 9.6 million deaths in 2022 according to the statistics of the World Health Organization. Cancer can begin in any part of the human organs when the normal cell loses the ability to control the division cycle, which may inhibit apoptosis. Cancer cells grow and multiply by activating the angiogenetic factors to build new capillaries that can supply tumor tissue with nutrients. Cancerous tumors spread into or invade nearby tissues and can travel to other organs in the body to form new carcinogenic tissue by metastasis. The goal of treatment is control growth of cancer cells, and induction the programmed cell death. Pyrimidines and its derivatives have been found as effective and valuable pharmacophoric units in medicinal chemistry to design and develop a wide range of bioactive compounds. The present review summarizes the advances in lead compounds of pyrimidines hybrids and their related heterocycles in the treatment of cancer. Moreover, the review also helps to intensify the drug development process by providing an understanding of the potential role of these hybridized pharmacophoric features as VEGFR-2 inhibitors.
嘧啶衍生物作为抗血管生成vegf -2抑制剂的意义综述
癌症是一种人体细胞不受控制地生长并扩散到身体其他部位的疾病。癌症是全球第二大死因,根据世界卫生组织的统计,2022年癌症造成960万人死亡。当正常细胞失去控制分裂周期的能力时,癌症可以在人体器官的任何部位开始,这可能会抑制细胞凋亡。癌细胞通过激活血管生成因子来生长和繁殖,从而建立新的毛细血管,为肿瘤组织提供营养。癌性肿瘤扩散或侵入附近组织,并可通过转移转移到身体其他器官形成新的致癌组织。治疗的目的是控制癌细胞的生长,诱导细胞程序性死亡。嘧啶及其衍生物在药物化学中是一种有效的、有价值的药效单位,可用于设计和开发各种具有生物活性的化合物。本文综述了嘧啶类杂环先导化合物及其相关杂环化合物在癌症治疗中的研究进展。此外,通过了解这些杂交的药理特征作为VEGFR-2抑制剂的潜在作用,该综述还有助于加强药物开发过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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