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Therefore, halogen bonding needs to be integrated into the molecular and drug design process.
Cheminformatic methods, such as Virtual Screening, constitute a vital part of modern drug design process.
Molecular docking is a widely used computational chemistry technique in the structure-based drug design process [1, 2].
Thus, such binding studies play an important role in the rational drug design process.
In the drug design process, one wants to construct chemical compounds with certain properties.
Designing a molecule that is selective in binding to one target rather than another is often considered a successful outcome in a drug design process.
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Knowledge about GPCR genes and their polymorphism is valuable information for drug design processes.
The characterisation of protein binding sites and of ligands is, at the first states of drug design processes, extremely important.
The bioactivity of chemical compounds can usually be explained in terms of common structural features, and the recognition of these features is the starting point in drug design processes.
In our case, molecular dynamics simulation study revealed a consistent value of the energy of the molecule throughout the time period of simulation, which is an indication of strong basis of the fact that the molecule has a stable structure as required for the virtual screening and drug designing processes.
Given the great flexibility of the neuraminidase active site, protein dynamics are also incorporated into the computer-aided drug-design process.
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