Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte Sant'Angelo, Via Cintia 4, 80126 Napoli, Italy.
Department of Chemistry and Biochemistry, Texas State University, San Marcos, TX 78666, USA.
Bioorg Med Chem Lett. 2019 Apr 1;29(7):859-869. doi: 10.1016/j.bmcl.2019.02.007. Epub 2019 Feb 7.
Ophiobolin A is a fungal secondary metabolite that was found to have significant activity against apoptosis-resistant glioblastoma cells through the induction of a non-apoptotic cell death, offering an innovative strategy to combat this aggressive cancer. The current article aims to make the bridge between the anti-cancer effects of ophiobolin A and its unique reaction with primary amines and suggests that pyrrolylation of lysine residues on its intracellular target protein(s) and/or phosphatidylethanolamine lipid is responsible for its biological effects. The article also discusses chemical derivatization of ophiobolin A to establish first synthetically generated structure-activity relationship. Finally, the reported total synthesis efforts toward the ophiobolin class of sesterterpenes are discussed and identified as a fertile area for improvement in pursuit of these molecules as anticancer agents.
蛇孢菌素 A 是一种真菌次级代谢产物,通过诱导非凋亡性细胞死亡,对凋亡抵抗型神经胶质瘤细胞具有显著的活性,为对抗这种侵袭性癌症提供了一种创新策略。本文旨在探讨蛇孢菌素 A 的抗癌作用与其与伯胺的独特反应之间的联系,并提出其细胞内靶蛋白赖氨酸残基的吡咯烷基化和/或磷脂酰乙醇胺脂质的磷酸化可能是其生物效应的原因。本文还讨论了蛇孢菌素 A 的化学衍生化,以建立首次合成的结构-活性关系。最后,讨论了报道的蛇孢菌素类甾体的全合成工作,并将其确定为改善这些分子作为抗癌剂的潜力领域。