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Finally, the standard Gibbs free energies of formation for the DyNi intermetallic compounds were estimated.
Furthermore, the partial molar volumes of those compounds were estimated following the theory developed by Kumar and Johnston.
Additionally, the partial molar volumes of those compounds were estimated following the theory developed by Kumar and Johnston.
The linearity ranges for all marker compounds were estimated, and satisfactory regression coefficient (r2 ≥ 0.99) values were obtained for all three selected markers.
The in vitro aldose reductase inhibitory activity of the prepared 1 7 compounds were estimated and compared with that of the initial compound (I).
The physicochemical parameters and the toxicity risk assessment of the synthesized compounds were estimated using Molinspiration and Osiris property calculation methods.
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The detection limits of the compounds are estimated to be 3 × 10-7 mol · l-1.
Identification of phenolic compounds was estimated on the basis of retention time.
There are more than 3000 potential drug targets surfaced as an outcome of Genomics revolution [1] and nearly 1033 compounds are estimated as drug-like chemical space [2].
The solubility of the compounds was estimated via the turbidimetric method using standard test buffers (pH 2.0 and pH 6.5) as previously described [23].
PC-SAFT parameters for 200 new compounds are estimated for different families of nonassociating compounds (alkanes, alkenes, alkynes, cycloalkenes, nitroalkanes, polynuclear aromatics, ketones, esters, sulphides, siloxanes, plasticizers, cyclo- and fluorinated-hydrocarbons, etc).
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