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The target compounds were structurally characterized by means of 1H NMR and 13C NMR spectrometric methods.
A detailed NMR spectrometric analysis of the methylated quercetin and luteolin derivatives confirmed the regiospecific methylation at the 4′-OH position.
Recently, global analyses of glycan signatures for pluripotency on the cell surface were reported, by direct observations of glycan structures by MALDI-TOF mass spectrometric and NMR spectrometric profiling in ESCs [ 5] and indirect observations of lectins by a lectin microarray in stem cells [ 6].
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Toward that end, H-NMR spectrometric analysis was used as a quantitative method for the noninvasive evaluation of biochemical processes involved in cell proliferation and growth arrest (Valonen et al, 2005).
The formation of probe 6 was characterized by FT-IR, 1H NMR, 13C NMR, mass spectrometric and single crystal X-ray diffraction analysis.
The nuclear magnetic resonance spectra (NMR) H, C NMR, and spectrometric dimensional techniques were recorded on spectrometer (Bruker-Avance DRX500), operating at 500 MHz (H-NMR) and 125 MHz (C-NMR).
Based on chromatographic profiling, nuclear magnetic resonance (NMR) and mass spectrometric analysis, the active compounds were identified as senkyunolide-H and its stereoisomer senkyunolide-I.
Iron III) complexes of three ligands (H2calm, H3anth and H3hyphS) have been studied by means of potentiometric, various spectroscopic (UV Vis, 1H NMR, IR), mass spectrometric, electrochemical and computational (DFT) methods.
The science of host metabolomics is growing with the development of applications such as NMR and Mass Spectrometric technologies.
Host response assays will have to be developed through the application of genomics and highly sensitive Mass Spectrometric, NMR or similar sensitive physical assays.
NMR and mass spectrometric analyses indicate that the DNA interstand cross-links contain a mixture of carbinolamine and Schiff base, with the carbinolamine forms of the linkages predominating in duplex DNA.
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