BDBM299876 4-[4-({[2-amino-5- (1-methyl-1H- imidazol-4- yl)pyridin-3- yl]oxy}methyl) piperidin-1- yl]-6-[(1- cyanocyclopropyl) methoxy]-N-(3,3- difluorobutan-2- yl)-1,3,5-triazine- 2-carboxamide::US9593097, Example 246

SMILES CC(NC(=O)c1nc(OCC2(CC2)C#N)nc(n1)N1CCC(COc2cc(cnc2N)-c2cn(C)cn2)CC1)C(C)(F)F

InChI Key InChIKey=JMOSFXPBLWUCMR-UHFFFAOYSA-N

Data  1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 299876   

TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Pfizer Inc

US Patent
LigandPNGBDBM299876(4-[4-({[2-amino-5- (1-methyl-1H- imidazol-4- yl)py...)
Show SMILES CC(NC(=O)c1nc(OCC2(CC2)C#N)nc(n1)N1CCC(COc2cc(cnc2N)-c2cn(C)cn2)CC1)C(C)(F)F
Show InChI InChI=1S/C28H34F2N10O3/c1-17(27(2,29)30)35-24(41)23-36-25(38-26(37-23)43-15-28(14-31)6-7-28)40-8-4-18(5-9-40)13-42-21-10-19(11-33-22(21)32)20-12-39(3)16-34-20/h10-12,16-18H,4-9,13,15H2,1-3H3,(H2,32,33)(H,35,41)
Affinity DataKi:  0.0400nMAssay Description:AXL enzyme inhibition (% inhibition, Kiapp and Ki values) by small molecule inhibitors was evaluated using a fluorescence-based microfluidic mobility...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid