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Receptor targets compound ADME

This raises the key test of target validation. Does a compound that has the appropriate potency, selectivity, and ADME properties, that is active in "predictive" animal models, and is free of other systems toxicology work in the targeted human disease state This is the ultimate test of a target-based drug discovery program. With the considerable compound attrition rates in moving from animals to diseased humans, this has not proven to be a predictable transition. A case in point is that of the NKl receptor activated by the peptide, substance P. [Pg.337]


See other pages where Receptor targets compound ADME is mentioned: [Pg.2]    [Pg.23]    [Pg.179]    [Pg.338]    [Pg.284]    [Pg.282]    [Pg.443]    [Pg.71]    [Pg.103]    [Pg.267]    [Pg.548]    [Pg.488]    [Pg.522]    [Pg.1023]    [Pg.232]    [Pg.347]    [Pg.117]    [Pg.208]    [Pg.437]    [Pg.449]    [Pg.291]    [Pg.262]    [Pg.219]    [Pg.488]    [Pg.522]    [Pg.60]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.320 , Pg.342 ]

See also in sourсe #XX -- [ Pg.320 , Pg.342 ]




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ADME

Target compounds

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