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3D-pharmacophores fingerprints

Beno BR, Mason JS. The design of combinatorial libraries using properties and 3D pharmacophore fingerprints. Drug Discov Today 2001 6(5) 251-8. [Pg.317]

Beno, B. R. and Mason, J. S. Combinatorial library design using both properties and 3D pharmacophore fingerprints. Book of Abstracts, 221st ACS National Meeting, San Diego, 2001. [Pg.375]

The use of 3D pharmacophore fingerprints in CADD applications can be broadly classified into the areas of design of combinatorial focused/diverse libraries, analyzing ligand-protein interactions and virtual HTS (vHTS) and protein selectivity. [Pg.194]

Figure 5.32. Some structurally diverse RGD antagonists matched through virtual screening using the RGD motif and 3D pharmacophore fingerprints. Figure 5.32. Some structurally diverse RGD antagonists matched through virtual screening using the RGD motif and 3D pharmacophore fingerprints.
Saeh, J.C., Lyne, P.D., Takasaki, B.K. and Cosgrove, D.A. (2005) Lead hopping using SVM and 3D pharmacophore fingerprints. Journal of Chemical Information and Modeling, 45,... [Pg.404]

See other pages where 3D-pharmacophores fingerprints is mentioned: [Pg.356]    [Pg.359]    [Pg.359]    [Pg.360]    [Pg.360]    [Pg.360]    [Pg.362]    [Pg.362]    [Pg.150]    [Pg.194]    [Pg.195]    [Pg.197]    [Pg.197]    [Pg.199]    [Pg.201]    [Pg.122]    [Pg.85]    [Pg.95]    [Pg.204]    [Pg.209]    [Pg.210]    [Pg.120]    [Pg.19]    [Pg.373]    [Pg.381]    [Pg.152]   
See also in sourсe #XX -- [ Pg.61 ]



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