Suppr超能文献

一些新型取代脒基-苯并咪唑基-呋喃基-苯基丙烯酸酯和萘并[2,1-b]呋喃羧酸酯的合成与抗肿瘤评价

Synthesis and antitumor evaluation of some new substituted amidino-benzimidazolyl-furyl-phenyl-acrylates and naphtho[2,1-b]furan-carboxylates.

作者信息

Hranjec M, Grdisa M, Pavelic K, Boykin D W, Karminski-Zamola G

机构信息

Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulicev trg 20, P.O. Box 177, HR-10000 Zagreb, Croatia.

出版信息

Farmaco. 2003 Dec;58(12):1319-24. doi: 10.1016/S0014-827X(03)00197-6.

Abstract

The multistep synthesis of a series of substituted amidino-benzimidazolyl-furyl-phenyl-acrylic acid's esters and substituted amidino-benzimidazolyl-naphtho[2,1-b]furan-carboxylic acid's esters is described starting from corresponding 3-(2-furyl)-2-phenyl-acrylic acids. The new compounds were tested on the cytostatic activities against malignant cell lines: pancreatic carcinoma (MiaPaCa2), breast carcinoma (MCF7), cervical carcinoma (HeLa), laryngeal carcinoma (Hep2), colon carcinoma (HT 29), melanoma (HBL), and human fibroblasts cell line (WI38). All compounds inhibited the proliferation of tumor cell lines. Inhibitory effect of examined compounds depended on concentration, but without significant difference among the type of tumor cells. The compounds 2 and 5 exerted very low inhibitory effect on the growth of human fibroblasts. Unsubstituted derivative 8 has not inhibited any tested cell lines.

摘要

描述了从相应的3-(2-呋喃基)-2-苯基丙烯酸开始,多步合成一系列取代脒基-苯并咪唑基-呋喃基-苯基-丙烯酸酯和取代脒基-苯并咪唑基-萘并[2,1-b]呋喃-羧酸酯的过程。对新化合物针对恶性细胞系进行了细胞抑制活性测试:胰腺癌细胞(MiaPaCa2)、乳腺癌细胞(MCF7)、子宫颈癌细胞(HeLa)、喉癌细胞(Hep2)、结肠癌细胞(HT 29)、黑色素瘤细胞(HBL)和人成纤维细胞系(WI38)。所有化合物均抑制肿瘤细胞系的增殖。所检测化合物的抑制作用取决于浓度,但在肿瘤细胞类型之间无显著差异。化合物2和5对人成纤维细胞的生长具有非常低的抑制作用。未取代的衍生物8未抑制任何测试细胞系。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验