BDBM466921 1-(4-{6-[(3R)-3- Methylmorpholin-4-yl]-2- {1H-pyrrolo[2,3-b]pyridin-4- yl}pyrimidin-4-yl}piperidin- 1-yl) propan-1-one::US10800774, Example 20

SMILES CCC(=O)N1CCC(CC1)c1cc(nc(n1)-c1ccnc2[nH]ccc12)N1CCOC[C@H]1C

InChI Key

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 466921   

TargetATR-interacting protein/Serine/threonine-protein kinase ATR(Homo sapiens (Human))
Board of Regents, The University of Texas System

US Patent
LigandPNGBDBM466921(1-(4-{6-[(3R)-3- Methylmorpholin-4-yl]-2- {1H-pyrr...)
Affinity DataIC50:  15nMAssay Description:Human full-length FLAG-TEV-ATR and His6-ATRIP were co-expressed in HEK293 cells. The cell pellet (20 g) was harvested and lysed in 100 mL of lysis bu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Board of Regents, The University of Texas System

US Patent
LigandPNGBDBM466921(1-(4-{6-[(3R)-3- Methylmorpholin-4-yl]-2- {1H-pyrr...)
Affinity DataIC50:  51nMAssay Description:Inhibitors of ATR kinase are effective at inhibiting the ATR-driven phosphorylation of the downstream target Chk1 kinase at Serine 345, following the...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent