Ahn Yongchel, Oh Sangtae, Lee Seong Jun, Park Byong-Gon, Park Yoon-Sun, Shin Woon-Seob, Jang Hyuk Jai, Park Jin Hoon, Kwon Daeho, Lee Seokjoon
Department of Hematology and oncology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung 210-711, Republic of Korea.
Department of Basic Science, Kwandong University College of Medicine, Gangneung 210-701, Republic of Korea.
Bioorg Med Chem Lett. 2014 Aug 1;24(15):3346-50. doi: 10.1016/j.bmcl.2014.05.098. Epub 2014 Jun 6.
A newly designed curcumin mimic library (11a-11k) with 2-ethylamino groups in a chalcone structure and variously substituted triazole groups as side chains was synthesized using the Huisgen 1,3-cycloaddition reaction between various alkynes (a-k) and an intermediate (10), with CuSO4 and sodium ascorbate in a solution mixture of chloroform, ethanol, and water (5:3:1) at room temperature for 5h. In the lactate dehydrogenase (LDH) release assay involving co-treatment with tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) and/or synthetic curcumin derivatives using TRAIL-resistant human CRT-MG astroglioma cells, the novel curcumin mimic library was found to effectively stimulate the cytotoxicity of TRAIL, causing mild cytotoxicity when administered alone. In particular, 11a and 11j are promising candidates for TRAIL-sensitizers with potential use in combination chemotherapy for brain tumors.
利用各种炔烃(a - k)与中间体(10)之间的惠斯根1,3 - 环加成反应,在室温下于氯仿、乙醇和水(5:3:1)的混合溶液中,以硫酸铜和抗坏血酸钠为催化剂,合成了一种新设计的姜黄素模拟物库(11a - 11k),该库在查尔酮结构中带有2 - 乙氨基基团,并带有各种取代的三唑基团作为侧链,反应时长为5小时。在涉及使用抗TRAIL的人CRT - MG星形胶质瘤细胞与肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)和/或合成姜黄素衍生物共同处理的乳酸脱氢酶(LDH)释放试验中,发现新型姜黄素模拟物库能有效刺激TRAIL的细胞毒性,单独给药时会引起轻微的细胞毒性。特别是,11a和11j有望成为TRAIL增敏剂,具有在脑肿瘤联合化疗中潜在应用的可能性。