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Fig. 1 Intensity of compounds present in the reference solution throughout the experiment.
Fig. 8 Solvent polarity versus Stokes shift and emission wavelengths of compounds M4 6 Fig. 9 Relative fluorescence intensity of compounds M1-6 in acetonitrile (1 × 10−5 M).
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The inset of Fig. 1 shows the change of absorption intensity of compound 2 at 241 nm with its concentration in CH3CN.
However, in the concentration range of 10−8 ~ 8 × 10−6 M, the absorption intensity of compound 2 in CH2Cl2 was dependent on concentration, as shown in Fig. 2.
Most metabolomic studies a decade ago had a relatively simple experimental design in which the intensities of compounds were compared between only two sample groups.
Moreover, the effect of increasing H2SO4 concentration was different on the CL intensity of the compounds.
We observed remarkable increase in the intensity of the compounds when proceeding the sequence.
In general, the fluorescence intensity of eluted compounds is stronger in hydrophobic circumstances.
Although prolonged proteasome inhibition has been shown to be the most optimal antimyeloma therapy in preclinical models, toxicity restricts dose intensity of these compounds in the clinical setting.
The luminescence intensity of this compound exceeds that for the europium benzoate ∼60 times at 77 K and ∼25 times at 295 K.
The quantity of scale formation was assumed to be directly proportional to the intensity of CaCO3 compound (reference code: 00-005-0586) analysed via XRD at 2θ = 29.406° (indicated by black arrow inside figure).
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