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The studies on oxidation reduction behavior of compounds of biological significance is of considerable value, as they provide deep insight into the biological relevant redox reactions of these compounds.
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Fig. 8 Predicting the reinforcement of behavior of compounds by Kraus Model.
This chapter demonstrates the use of powerful software tools that reliably give a kinetic model of decomposition behavior of compounds such as Butadiene-1, 2 and a nitro aromatic residue based on DTA/DSC measurements at a range of different heating rates, allowing to calculate the adiabatic induction time for different temperatures based on model parameters.
The thermal behavior of compounds 1 and 2 was investigated.
For all these reasons the understanding of the chemical as well as the physical behavior of compounds in these three states of the matter was necessary.
Again, this gives a more realistic view of the conformational behavior of compound 1. Figure 3 Pseudorotation wheel for compounds 1 and 2. Contour lines indicate the total RMSD with the experimental data (Hz).
The voltammetric behavior of compound 7e was studied (Fig. 5).
Our data therefore suggested an agonistic behavior of compound 1 for the interaction of LFA-1 with ICAM-1.
However, since the behavior of these compounds does not differ much, the natural compounds show a behavior similar to that of the studied synthetic compounds.
The dibenzothiophene derivatives of compound 2 and compounds 4 6 were synthesized successfully and the self-association behavior of these compounds in CH2Cl2 and CH3CN were investigated.
While the use of Kow in predicting soil sorption behavior of nonpolar compounds works fairly well, the application of Kow for polar or ionizable compounds, such as many antibiotics, may be inaccurate.
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