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A selective inhibitor of cyclic AMP-dependent protein kinase, N-2-bromocinnamyl(amino)ethyl-5-isoquinolinesulfonamide (H-89), inhibits phosphatidylcholine biosynthesis in HeLa cells

机译：环状AMP依赖性蛋白激酶的选择性抑制剂N- 2-溴肉桂基（氨基）乙基 -5-异喹啉磺酰胺（H-89）抑制HeLa细胞中磷脂酰胆碱的生物合成

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Geilen Christoph C.; Wieprecht Marcus; Wieder Thomas; Reutter Werner;
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年度 1992
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1. A selective inhibitor of cyclic AMP‐dependent protein kinase, N‐[2‐bromocinnamyl(amino)ethyl]‐5‐isoquinolinesulfonamide (H‐89), inhibits phosphatidylcholine biosynthesis in HeLa cells [J] . Geilen Christoph C., Reutter Werner, Wieder Thomas, FEBS Letters . 1992,第3期

机译：N- [2-溴肉桂基（氨基）乙基] -5-异喹啉磺酰胺（H-89）选择性的环状AMP依赖性蛋白激酶抑制剂可抑制HeLa细胞中的磷脂酰胆碱生物合成
2. A specific adenylyl cyclase inhibitor (DDA) and a cyclic AMP-dependent protein kinase inhibitor (H-89) block the action of equine growth hormone on in vitro maturation of equine oocytes [J] . Pereira Gabriel Ribas, Luis Lorenzo Pedro, Carneiro Gustavo Ferrer, Zygote . 2015,第6期

机译：特定的腺苷酸环化酶抑制剂（DDA）和环状AMP依赖性蛋白激酶抑制剂（H-89）阻止马生长激素对马卵母细胞体外成熟的作用
3. Inhibition of cyclic AMP-dependent kinase by expression of a protein kinase inhibitor/enhanced green fluorescent fusion protein attenuates angiotensin II-induced type 1 AT1 receptor mRNA down-regulation in vascular smooth muscle cells. [J] . Wang X, Murphy TJ Molecular pharmacology. . 1998,第3期

机译：通过蛋白激酶抑制剂/增强型绿色荧光融合蛋白的表达抑制环状AMP依赖性激酶可减弱血管紧张素II诱导的1型AT1受体mRNA在血管平滑肌细胞中的下调。
4. Noninvasive in vivo mapping of intracellular signaling proteins using a pairing of targeted and untargeted fluorescently labeled small molecule kinase inhibitors [C] . Kenneth M. Tichauer, Lei Wang, Allison Solanki, Conference on Visualizing and Quantifying Drug Distribution in Tissue . 2020

机译：使用对靶向和未明确的荧光标记的小分子激酶抑制剂的配对的细胞内信号蛋白的体内测绘的非侵入性
5. Small Molecule Inhibitors of Cell Migration and The Subcellular Localization of Raf Kinase Inhibitor Protein [D] . Argueta, Christian 2012

机译：细胞迁移的小分子抑制剂和Raf激酶抑制剂蛋白的亚细胞定位
6. N-2-bromocinnamyl(amino)ethyl-5-isoquinolinesulphonamide (H-89) inhibits incorporation of choline into phosphatidylcholine via inhibition of choline kinase and has no effect on the phosphorylation of CTP:phosphocholine cytidylyltransferase. [O] . M Wieprecht, T Wieder, C C Geilen 1994

机译：N- 2-溴肉桂基（氨基）乙基 -5-异喹啉磺酰胺（H-89）通过抑制胆碱激酶来抑制胆碱掺入磷脂酰胆碱并且对CTP：磷酸胆碱胞苷转移酶的磷酸化没有影响。
7. Effects of protein kinase inhibitors and protein phosphatase inhibitors on cyclic AMP-dependent down-regulation of vesicular monoamine transport in pheochromocytoma PC12 cells [O] . Nobuo Nakanishi, Satoshi Onozawa, Reiko Matsumoto, 1995

机译：蛋白激酶抑制剂和蛋白磷酸酶抑制剂对嗜铬细胞瘤PC12细胞中环AMP依赖的水泡单胺转运的下调
8. Characterization of the Sites Phosphorylated on Tyrosine Hydroxylase by Ca(2+) and Phospholipid-Dependent Protein Kinase, Calmodulin-Dependent Multiprotein Kinase and Cyclic AMP-Dependent Protein Kinase [R] . Vulliet, P. R., Woodgett, J. R., Ferrari, S., 1985

机译：通过Ca（2+）和磷脂依赖性蛋白激酶，钙调蛋白依赖性多蛋白激酶和环amp依赖性蛋白激酶在酪氨酸羟化酶上磷酸化位点的表征

A selective inhibitor of cyclic AMP-dependent protein kinase, N-2-bromocinnamyl(amino)ethyl-5-isoquinolinesulfonamide (H-89), inhibits phosphatidylcholine biosynthesis in HeLa cells

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