Department of Nuclear Medicine, Peking Union Medical College & Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, Beijing 100730, China.
Molecules. 2009 Dec 18;14(12):5339-48. doi: 10.3390/molecules14125339.
To seek novel antitumor agents, we designed and synthesized new 1-tryptophan analogs based on tryptophan catabolism. 1-Alkyl-tryptophan analogues including 1-ethyltryptophan (1-ET), 1-propyltryptophan (1-PT), 1-isopropyltryptophan (1-isoPT) and 1-butyltryptophan (1-BT) were synthesized from tryptophan. We examined whether those compounds had the antiproliferative effects on SGC7901 and HeLa cells line by using MTT assay in vitro, respectively. Compared to tryptophan, all targeted compounds efficiently inhibited proliferation of two cancer cell lines at 2 mmol/L for 48 hours. Among these tryptophan analogs, 1-BT showed the most powerful cytotoxicity against SGC7901 and HeLa cells at 1 mmol/L and 2 mmol/L concentration. These data suggest that some specific tryptophan analogs could be developed as potential anti-neoplastic agents.
为了寻找新型抗肿瘤药物,我们基于色氨酸代谢设计并合成了新的 1-色氨酸类似物。从色氨酸合成了 1- 烷基色氨酸类似物,包括 1-乙基色氨酸(1-ET)、1-丙基色氨酸(1-PT)、1-异丙基色氨酸(1-isoPT)和 1-丁基色氨酸(1-BT)。我们通过 MTT 法分别检测了这些化合物对 SGC7901 和 HeLa 细胞系的体外增殖抑制作用。与色氨酸相比,所有靶向化合物在 2 mmol/L 浓度下 48 小时均能有效抑制两种癌细胞系的增殖。在这些色氨酸类似物中,1-BT 在 1 mmol/L 和 2 mmol/L 浓度下对 SGC7901 和 HeLa 细胞表现出最强的细胞毒性。这些数据表明,一些特定的色氨酸类似物可能被开发为潜在的抗肿瘤药物。