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姜黄素是钙/钙调蛋白依赖性蛋白激酶 II 的抑制剂。

Curcumin is an inhibitor of calcium/calmodulin dependent protein kinase II.

机构信息

Molecular Neurobiology Division, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala, India.

出版信息

Bioorg Med Chem. 2012 Oct 15;20(20):6040-7. doi: 10.1016/j.bmc.2012.08.029. Epub 2012 Aug 30.

Abstract

Calcium/calmodulin dependent protein kinase II (CaMKII) is involved in the mechanisms underlying higher order brain functions such as learning and memory. CaMKII participates in pathological glutamate signaling also, since it is activated by calcium influx through the N-methyl-d-aspartate type glutamate receptor (NMDAR). In our attempt to identify phytomodulators of CaMKII, we observed that curcumin, a constituent of turmeric and its analogs inhibit the Ca(2+)-dependent and independent kinase activities of CaMKII. We further report that a heterocyclic analog of curcumin I, (3,5-bis[β-(4-hydroxy-3-methoxyphenyl)ethenyl]pyrazole), named as pyrazole-curcumin, is a more potent inhibitor of CaMKII than curcumin. Microwave assisted, rapid synthesis of curcumin I and its heterocyclic analogues is also reported.

摘要

钙/钙调蛋白依赖性蛋白激酶 II(CaMKII)参与学习和记忆等高级脑功能的机制。CaMKII 还参与病理性谷氨酸信号转导,因为它通过 N-甲基-D-天冬氨酸型谷氨酸受体(NMDAR)的钙内流而被激活。在我们试图鉴定 CaMKII 的植物调节剂的过程中,我们观察到姜黄素,姜黄的一种成分及其类似物,抑制 Ca(2+)依赖性和非依赖性激酶活性的 CaMKII。我们进一步报告说,姜黄素 I 的杂环类似物(3,5-双[β-(4-羟基-3-甲氧基苯基)乙烯基]吡唑),命名为吡唑姜黄素,是比姜黄素更有效的 CaMKII 抑制剂。还报告了姜黄素 I 及其杂环类似物的微波辅助快速合成。

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