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一些新型四唑并[1,5-a]嘧啶衍生物的区域选择性一锅合成及抗增殖和促凋亡作用。

Regioselective one-pot synthesis and anti-proliferative and apoptotic effects of some novel tetrazolo[1,5-a]pyrimidine derivatives.

机构信息

Chemistry Department (Organic Chemistry Division), Faculty of Science, Beni-Suef University, Egypt.

出版信息

Bioorg Med Chem. 2010 Apr 1;18(7):2639-44. doi: 10.1016/j.bmc.2010.02.028. Epub 2010 Feb 20.

Abstract

An easy and efficient route for the synthesis of some tetrazolo[1,5-a]-pyrimidine derivatives was described through the reaction of sodium salts of formyl cycloalkanones with 5-aminotetrazole monohydrate. The derivative 6,7,8,9-tetrahydrotetrazolo[1,5-a]quinazoline (6b) has profound anti-tumor cytotoxic effects against Ehrlich ascites carcinoma (EAC) both in vivo and in vitro and against hepatocellular carcinoma (HepG2) cell line in vitro. These anti-tumor effects may be mediated via stimulation of cell cycle arrest and apoptosis through down-regulation of Bcl-2 and up-regulation of p53 transcription factors.

摘要

通过甲酰环烷酮的钠盐与 5-氨基四唑一水合物的反应,描述了合成一些四唑并[1,5-a]嘧啶衍生物的简单高效途径。衍生物 6,7,8,9-四氢四唑并[1,5-a]喹唑啉(6b)对艾氏腹水癌(EAC)具有深刻的体内和体外抗肿瘤细胞毒性作用,对体外肝癌(HepG2)细胞系也具有抗肿瘤作用。这些抗肿瘤作用可能是通过下调 Bcl-2 和上调 p53 转录因子来诱导细胞周期停滞和细胞凋亡来介导的。

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