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SMILES: C1CC(CCO1)c1cc2nc(Nc3cccc(c3)N3CCOCC3)ncc2[nH]1

InChI Key: InChIKey=KCJWOBHDPCYAJG-UHFFFAOYSA-N

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 372161   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Receptor-interacting serine/threonine-protein kinase 2


(Homo sapiens (Human))
BDBM372161
PNG
(N-(3- morpholino- phenyl)-6- (tetrahydro-2H- pyran...)
Show SMILES C1CC(CCO1)c1cc2nc(Nc3cccc(c3)N3CCOCC3)ncc2[nH]1
Show InChI InChI=1S/C21H25N5O2/c1-2-16(12-17(3-1)26-6-10-28-11-7-26)23-21-22-14-20-19(25-21)13-18(24-20)15-4-8-27-9-5-15/h1-3,12-15,24H,4-11H2,(H,22,23,25)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>500n/an/an/an/an/an/a



UNIVERSITY HEALTH NETWORK

US Patent


Assay Description
Active RIPK2 was purchased from Life Technologies as His-tagged of catalytic domain (amin acids 1-299) of human RIPK2 kinase expressed in insect cell...


US Patent US10875863 (2020)

More data for this
Ligand-Target Pair
Receptor-interacting serine/threonine-protein kinase 2


(Homo sapiens (Human))
BDBM372161
PNG
(N-(3- morpholino- phenyl)-6- (tetrahydro-2H- pyran...)
Show SMILES C1CC(CCO1)c1cc2nc(Nc3cccc(c3)N3CCOCC3)ncc2[nH]1
Show InChI InChI=1S/C21H25N5O2/c1-2-16(12-17(3-1)26-6-10-28-11-7-26)23-21-22-14-20-19(25-21)13-18(24-20)15-4-8-27-9-5-15/h1-3,12-15,24H,4-11H2,(H,22,23,25)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>500n/an/an/an/an/an/a



National Taiwan University



Assay Description
RIPK2 activity was measured using an indirect ELISA detection system. His—RIPK2 (0.6 nM) was incubated in the presence of 6 μM ATP (Sigma cat # ...


J Med Chem 51: 2795-806 (2008)


BindingDB Entry DOI: 10.7270/Q289186K
More data for this
Ligand-Target Pair