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In silico docking studies were performed to screen several compounds containing pyrimidine scaffold against CAMKIV.
The molecular features that govern their bioactivity were explored through in silico docking experiments.
The binding modes between chromenylchalcone 11 and aurora kinases were elucidated using in silico docking experiments.
The binding ability of mimosine to ERα was predicted by in silico docking method.
To elucidate the possible interaction between naringenin derivatives and CDK2, in silico docking study was performed.
The anticipated binding mode of these analogs was confirmed by performing the in silico docking experiments.
The experimental studies were compared with in silico docking results conducted with the help of iGemdock.
In silico docking studies predicted similar binding pattern of compound 19 on androgen receptor as hydroxyflutamide.
We suggest that TMD method may help in discriminating between ligands generated by in silico docking.
In order to investigate the binding mechanisms of these inhibitors, in silico docking studies were applied.
In silico docking studies on Human topoisomerase IIbeta (PDB Id: 3QX3) have been performed for all molecules (KM10 17) synthesized.
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