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蛋白激酶CK2的新型抑制剂,苯并咪唑和苯并三唑类似物。

New inhibitors of protein kinase CK2, analogues of benzimidazole and benzotriazole.

作者信息

Bretner Maria, Najda-Bernatowicz Andzelika, Łebska Maja, Muszyńska Grazyna, Kilanowicz Anna, Sapota Andrzej

机构信息

Institute of Biochemistry and Biophysics, Pawińskiego 5a, 02-106, Warsaw, Poland.

出版信息

Mol Cell Biochem. 2008 Sep;316(1-2):87-9. doi: 10.1007/s11010-008-9827-0. Epub 2008 Jun 12.

Abstract

Derivatives of 4,5,6,7-tetrabromobenzotriazole (TBBt) and 4,5,6,7-tetrabromobenzimidazole (TBBi) with IC50 in the low micromolar range and with high selectivity belong to the most promising inhibitors of protein kinase CK2 (casein kinase 2). Treatment of various cell lines with TBBt, TBBi or 2-dimethylamino-4,5,6,7-tetrabromo-1H-benzimidazole (DMAT) affected cell viability with simultaneous induction of apoptosis. The inhibitory activity of newly synthesized hydroxyalkyl derivatives of TBBi and TBBt depends on the length of the alkyl chain. The hydroxypropyl substituted derivatives show higher or similar inhibitory activity than the parent compounds when tested with human protein kinase CK2. To test the distribution of this class of compounds in mammals, [14C] TBBi was synthesized.

摘要

4,5,6,7-四溴苯并三唑(TBBt)和4,5,6,7-四溴苯并咪唑(TBBi)的衍生物,其半数抑制浓度(IC50)处于低微摩尔范围且具有高选择性,属于最有前景的蛋白激酶CK2(酪蛋白激酶2)抑制剂。用TBBt、TBBi或2-二甲基氨基-4,5,6,7-四溴-1H-苯并咪唑(DMAT)处理各种细胞系会影响细胞活力,同时诱导细胞凋亡。新合成的TBBi和TBBt的羟烷基衍生物的抑制活性取决于烷基链的长度。当用人蛋白激酶CK2进行测试时,羟丙基取代的衍生物显示出比母体化合物更高或相似的抑制活性。为了测试这类化合物在哺乳动物体内的分布,合成了[14C]TBBi。

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