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- W2951496337 abstract "We have identified moderately potent and selective inhibitors of CSF-1R tyrosine kinase activity.1 A preliminary SAR study resulted in the identification of compounds 11 and 20 as the most potent analogues in the series (IC50 = 0.18 μM). The 3-D-conformation of the 4-(N-alkyl-N-phenyl)-aminoquinazolines has been proposed to be important to the overall selectivity and activity." @default.
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- W2951496337 date "1997-02-01" @default.
- W2951496337 modified "2023-09-25" @default.
- W2951496337 title "The synthesis and SAR of new 4-(N-alkyl-N-phenyl)amino-6,7-dimethoxyquinazolines and 4-(N-alkyl-N-phenyl)aminopyrazolo[3,4-d]pyrimidines, inhibitors of CSF-1R tyrosine kinase activity" @default.
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- W2951496337 doi "https://doi.org/10.1016/s0960-894x(97)00035-8" @default.
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