BDBM277385 US10072025, Example 3-19::US10072025, Example 3-20::tert-butyl 4-ethyl-4-[3-({3- methyl-4-[(6R or 6S- methyl-1,4-oxazepan-4-yl) carbonyl]phenyl} amino)- 4-oxo-4,5-dihydro-1H- pyrazolo [4,3-c]pyridin-1- yl] piperidine-1- carboxylate (Peak A, separated by SFC, using AD-H column, eluting with 25% isopropanol (0.1% NPA) in CO2, retention time: 5.3 minutes.)
SMILES CCC1(CCN(CC1)C(=O)OC(C)(C)C)n1nc(Nc2ccc(C(=O)N3CCOCC(C)C3)c(C)c2)c2c1cc[nH]c2=O
InChI Key
Data 4 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 277385
Affinity DataIC50: 1.23nMT: 2°CAssay Description:The ability of compounds to inhibit the activity of JAK1, JAK2, JAK3, and Tyk2 was measured using a recombinant purified GST-tagged catalytic domain ...More data for this Ligand-Target Pair
Affinity DataIC50: 0.990nMT: 2°CAssay Description:The ability of compounds to inhibit the activity of JAK1, JAK2, JAK3, and Tyk2 was measured using a recombinant purified GST-tagged catalytic domain ...More data for this Ligand-Target Pair