Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), S.A.S Nagar, Mohali, Punjab, India.
School of Pharmaceutical Education and Research (SPER), Jamia Hamdard, New Delhi, India.
Eur J Med Chem. 2021 Apr 15;216:113321. doi: 10.1016/j.ejmech.2021.113321. Epub 2021 Feb 24.
β-Carbolines are indole alkaloids having a tricyclic pyrido[3,4-b]indole ring in their structure. Since the isolation of first β-carboline from Peganum harmala in 1841, the isolation and synthesis of various β-carboline derivatives surged in the following centuries. β-Carboline derivatives due to their widespread availability from natural sources, structural flexibility, quick reactivity and interaction with varied anticancer targets such as DNA (intercalation, groove binding, etc.), enzymes (GPX4, topoisomerases, kinases, etc.) and proteins (tubulin, ABCG2/BRCP1, etc.) have established themselves as promising lead compounds for the synthesis of various anticancer active agents. The current review covers the synthesis and isolation, anticancer activity, mechanism of action and SAR of various β-carboline containing molecules, its derivatives and congeners.
β-咔啉是吲哚生物碱,其结构中具有三环吡啶并[3,4-b]吲哚环。自 1841 年从 Peganum harmala 中分离出第一个β-咔啉以来,在随后的几个世纪中,各种β-咔啉衍生物的分离和合成如雨后春笋般涌现。β-咔啉衍生物由于其广泛存在于天然来源中、结构灵活性、快速反应性以及与多种抗癌靶标(如 DNA(嵌入、沟结合等)、酶(GPX4、拓扑异构酶、激酶等)和蛋白质(微管蛋白、ABCG2/BRCP1 等)的相互作用,已成为合成各种抗癌活性物质的有前途的先导化合物。本综述涵盖了各种含β-咔啉的分子、其衍生物和同系物的合成与分离、抗癌活性、作用机制和 SAR。