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Charles W. Koch Richard M. Milberg Robert J. Katt J. Hodge Markgraf P. M. Wege 《Journal of heterocyclic chemistry》1974,11(4):475-479
High resolution mass spectra of compounds 1—8 were investigated. For the quinolines (1–3) the absence of major peaks other than M+ and (M-1)+ reflects the stability of those systems. The N-oxides (4–6) all exhibit major peaks at M+, (M-16)+, and (M-17)+. In addition, 4 shows prominent fragmentations reflecting loss of hydrogen and carbon monoxide. The pathways are related to the geometries of the N-oxides; deuterated compounds (7–8) aided these assignments. 相似文献
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Background
Neurons require an elaborate system of intracellular transport to distribute cargo throughout axonal and dendritic projections. Active anterograde and retrograde transport of mitochondria serves in local energy distribution, but at the same time also requires input of ATP. Here we studied whether brain-type creatine kinase (CK-B), a key enzyme for high-energy phosphoryl transfer between ATP and CrP in brain, has an intermediary role in the reciprocal coordination between mitochondrial motility and energy distribution. Therefore, we analysed the impact of brain-type creatine kinase (CK-B) deficiency on transport activity and velocity of mitochondria in primary murine neurons and made a comparison to the fate of amyloid precursor protein (APP) cargo in these cells, using live cell imaging. 相似文献
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