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The linear dynamic range is the data range that the detector can discriminate the responses from the different concentration of a given compounds and it is linearly proportional to its concentration.
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Until very recently, it was not possible to quantify the uptake of a given compound at single cell level.
To date, identification of the topological nature of a given compound material demands specific determination of the appropriate topological invariant through detailed electronic structure calculations.
Reactions that directly install nitrogen into C H bonds of complex molecules are significant because of their potential to change the chemical and biological properties of a given compound.
Furthermore, the lipophilicity of a given compound also reflects a critical physicochemical trait for neuroimaging radiotracers due to its direct relationship to membrane permeability, solubility in water, and entropic contribution to binding.
A correlation between the parameters characterising biological activity and the NQR spectral parameters describing chemical properties of a given compound, permits drawing conclusions on biological effectiveness of compounds from a certain group.
For example, what dose level in the ambient water of a small fish model would be equivalent to 10 ppm of a given compound in the rat's drinking water?
In particular, the rate constant of the second kind for the exclusive growth of a given compound is a function of the n rate constants of the first kind measured on the complete couple where all the intermediate phases grow simultaneously.
RNA-based SIP technologies represent a significant leap forward for culture-independent 'functional phylogeny' analyses, where specific consumption of a given compound carrying a 13C signature can be associated with the small subunit ribosomal RNA molecules of the microbes that consume it.
Anti-HCV ability of a given compound was estimated by combining its EC50 with SI values.
Apart from the implications discussed below, our study demonstrates the importance of investigating separately the enantiomers of a given compound.
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