药效团
免疫监视
肿瘤坏死因子α
细胞因子
化学
细胞凋亡
配体(生物化学)
立体化学
免疫学
计算生物学
癌症研究
医学
受体
生物
肿瘤细胞
生物化学
作者
Nicholas T. Jacob,Jonathan W. Lockner,Vladimir V. Kravchenko,Kim D. Janda
标识
DOI:10.1002/anie.201402133
摘要
Abstract Tumor necrosis factor (TNF)‐related apoptosis‐inducing ligand (TRAIL) is an immunosurveillance cytokine that kills cancer cells but demonstrates little toxicity against normal cells. While investigating the TRAIL‐inducing imidazolinopyrimidinone TIC10, a misassignment of its active structure was uncovered. Syntheses of the two isomers, corresponding to the published and reassigned structures, are reported. The ability of each to induce TRAIL expression in macrophages was investigated and it was found that only the compound corresponding to the reassigned structure shows the originally reported activity; the compound corresponding to the published structure is inactive. Importantly, this structural reassignment has furnished a previously unknown antitumor pharmacophore.
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