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In silico ADMET studies were performed on compounds retrieved from virtual screening in compliance with the standard ranges.
Based on cyclic voltammetry investigations, absorption and fluorescence spectroelectrochemistry were then performed on compounds 1, 2, 3 and their parent reduced radicals 1a, 2a, 3a.
Substructure analysis was performed on compounds having a favorable assessment by target prediction and docking (i.e. those compounds whose docking scores were below the threshold for all three targets).
In the next step docking and further substructure analysis were performed on compounds of the focused RECAP library, which were predicted as A1R/A2AR PDE10A multi-target ligands from the ligand-based side in the previous step.
Density functional theory and time-dependent density functional theory calculations at the B3LYP/LanL2DZ+6-31G∗ level were performed on compounds 1 3 to rationalize their experimental absorption spectra.
Extensive study has been performed on compounds of the form, where M represents a monovalent cation and An is either uranium, neptunium, or plutonium.
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This paper describes the experimentation of the author's recent study of surface areal irradiance (SAI) method performed on compound parabolic collector (CPC) with low acceptance angle.
In this research, the optical analyses are performed on compound parabolic collector with low acceptance angle (6°) to optimize the receiver position.
The in silico protein ligand docking using autodock 4.1 was successfully performed on compound 5 with significant binding energy value of −5.58 kcal/mol.
Temperature dependent X-ray powder diffractometry (TDXD) has been performed on compound 1 in order to follow the structural transformations that occur during the heating process.
N-Benzylation was then performed on compound 6 c.
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