Inhibition of the equilibrative nucleoside transporter 1 and activation of A2A adenosine receptors by 8-(4-chlorophenylthio)-modified cAMP analogs and their hydrolytic products.
第一作者:
Oliver,Waidmann
第一单位:
Department of Medicine I, University Hospital Frankfurt, D-60590 Frankfurt, Germany.
作者:
医学主题词
氨基酸特征结构(Amino Acid Motifs);动物(Animals);细胞凋亡(Apoptosis);细胞系(Cell Line);着色剂(Coloring Agents);环AMP(Cyclic AMP);环AMP依赖性蛋白激酶类(Cyclic AMP-Dependent Protein Kinases);平衡核苷转移子1(Equilibrative Nucleoside Transporter 1);人类(Humans);水解作用(Hydrolysis);PC12细胞(PC12 Cells);磷酰化(Phosphorylation);大鼠(Rats);受体, 腺苷A2A(Receptor, Adenosine A2A);四唑鎓盐类(Tetrazolium Salts);噻唑类(Thiazoles)
DOI
10.1074/jbc.M109.056622
PMID
19801629
发布时间
2021-10-20
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