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Virtual screening structure-based drug design/discovery

Drug design, based on crystal structures of target incorporated with substrate or inhibitor (primarily for enzymes). More useful for lead optimization than for primary discovery. Can be configured to serve as electronic ( virtual ) random screen. 1980s-present. [Pg.325]

See other pages where Virtual screening structure-based drug design/discovery is mentioned: [Pg.3]    [Pg.147]    [Pg.184]    [Pg.306]    [Pg.244]    [Pg.282]    [Pg.417]    [Pg.222]    [Pg.150]    [Pg.397]    [Pg.597]    [Pg.97]    [Pg.306]    [Pg.157]    [Pg.274]    [Pg.271]    [Pg.357]    [Pg.37]    [Pg.41]    [Pg.419]    [Pg.512]    [Pg.79]    [Pg.16]    [Pg.301]    [Pg.531]    [Pg.231]    [Pg.190]    [Pg.259]    [Pg.1]    [Pg.177]    [Pg.272]    [Pg.53]    [Pg.89]    [Pg.341]    [Pg.342]    [Pg.276]    [Pg.78]    [Pg.123]    [Pg.344]    [Pg.218]    [Pg.322]    [Pg.188]    [Pg.244]    [Pg.50]    [Pg.37]    [Pg.40]    [Pg.4]    [Pg.575]    [Pg.2]   
See also in sourсe #XX -- [ Pg.29 ]



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Based Drug Design

Based Screens

Design Bases

Design structures

Discovery screening

Drug Screens

Drug design/discovery

Drug design/discovery structure-based

Drug design/discovery virtual screening

Drug discovery screening

Drug structure

Drug structure-based

Drugs screening

Screen design

Screen structure-based

Screen virtual

Screening designs

Screening structure-based

Screening virtual

Structure based design

Structure designable

Structure drug design

Structure screening

Structure-based drug design

Structure-based virtual screening

Virtual structure-based

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