The phrase "above mentioned compounds" is correct and usable in written English.
It can be used when referring to compounds that have been previously mentioned in the text.
Example: "The results of the experiments on the above mentioned compounds indicate significant improvements in efficiency."
Alternatives: "aforementioned compounds" or "previously mentioned compounds".
This method has been successfully used for preconcentration and analysis of above mentioned compounds in different real water samples.
The mutagenic and carcinogenic potency of the above mentioned compounds as well as their presence in feces, proposed mode of action and potential role in the initiation and promotion of human colorectal cancer are discussed.
After synthesis and analysis of the above mentioned compounds, whole cell biotransformation reactions with E. coli hosting the recombinantly expressed hydantoinase employing pNO2PheDU ((R/S -4a) as substR/S -4are performed.
All of the above mentioned compounds have been shown to be toxic to S. exigua, and at least bacterial spores, Cry toxins, and zwittermicin are found in Xentari™.
First, the effects of low doses of 2-DG seem to preferentially affect actively forming capillaries, an effect that was not demonstrated with the above mentioned compounds.
All the above mentioned compounds compete for the substrate binding part of the catalytic site.
Here we report the formation of hexameric water clusters with chair configuration in the crystal structure of above mentioned compound.
In a recent study on the polymorphism of a hexa-substituted benzene derivative, Hexakis (4-cyanophenyloxy) benzene, it was suggested that one can get four different polymorphic forms of the above mentioned compound when crystallising it from melt [34].
The CV plots for the above mentioned compound channels are shown in Figure 4, in which is also provided the simulation results to demonstrate the accuracy of the derived expressions.
The experimental data for all measured systems are finally compared with the corresponding literature data in the absence of the above mentioned cyclic compounds to identify their promotion effects.
In another set of experiment the above mentioned six compounds again demonstrated an extremely potent inhibition on the isolated neutrophils with IC50, <0.1, <0.1, 1.7, 0.2, 2.4 and 0.2 μg mL-1 respectively (Figure 2A).
