Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10593510 | Bioorganic & Medicinal Chemistry Letters | 2012 | 4 Pages |
Abstract
We investigated several 2-phenylquinazolines with different substitutions at position 4 for their BCRP inhibition. Compounds with phenyl ring attached via an amine-containing linker at position 4 were found to be potent inhibitors of BCRP. In general compounds with meta substitution of phenyl ring at position 4 were found to have higher inhibitory effect, compound 12 being the most potent and selective towards BCRP.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kapil Juvale, Michael Wiese,