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BDBM196074 US9206199, 179

SMILES: O=C(Cc1ccc(nc1)-n1cnnn1)N1CCN2C[C@H](OC[C@@H]2C1)c1ccc2nonc2c1

InChI Key: InChIKey=BZFLRKRZTBWDNX-JAXKJVMINA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 196074   
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
ATP-sensitive inward rectifier potassium channel 1


(Homo sapiens (Human))
BDBM196074
PNG
(US9206199, 179)
Show SMILES O=C(Cc1ccc(nc1)-n1cnnn1)N1CCN2C[C@H](OC[C@@H]2C1)c1ccc2nonc2c1 |r|
Show InChI InChI=1/C21H21N9O3/c31-21(7-14-1-4-20(22-9-14)30-13-23-26-27-30)29-6-5-28-11-19(32-12-16(28)10-29)15-2-3-17-18(8-15)25-33-24-17/h1-4,8-9,13,16,19H,5-7,10-12H2/t16-,19-/s2
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US Patent
n/an/a 180n/an/an/an/an/an/a



Merck Sharp & Dohme Corp.

US Patent


Assay Description
The ROMK channel functional thallium flux assay is performed in 384 wells, using the FLIPR-Tetra instrument. HEK-hKir1.1 cells are seeded in Poly-D-L...


US Patent US9206199 (2015)


BindingDB Entry DOI: 10.7270/Q2VH5MND
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM196074
PNG
(US9206199, 179)
Show SMILES O=C(Cc1ccc(nc1)-n1cnnn1)N1CCN2C[C@H](OC[C@@H]2C1)c1ccc2nonc2c1 |r|
Show InChI InChI=1/C21H21N9O3/c31-21(7-14-1-4-20(22-9-14)30-13-23-26-27-30)29-6-5-28-11-19(32-12-16(28)10-29)15-2-3-17-18(8-15)25-33-24-17/h1-4,8-9,13,16,19H,5-7,10-12H2/t16-,19-/s2
PDB
MMDB

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Article
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n/an/a>1.00E+4n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human ERG by electrophysiology method


Bioorg Med Chem Lett 26: 5695-5702 (2016)


Article DOI: 10.1016/j.bmcl.2016.10.064
BindingDB Entry DOI: 10.7270/Q2F191PS
More data for this
Ligand-Target Pair
ATP-sensitive inward rectifier potassium channel 1


(Homo sapiens (Human))
BDBM196074
PNG
(US9206199, 179)
Show SMILES O=C(Cc1ccc(nc1)-n1cnnn1)N1CCN2C[C@H](OC[C@@H]2C1)c1ccc2nonc2c1 |r|
Show InChI InChI=1/C21H21N9O3/c31-21(7-14-1-4-20(22-9-14)30-13-23-26-27-30)29-6-5-28-11-19(32-12-16(28)10-29)15-2-3-17-18(8-15)25-33-24-17/h1-4,8-9,13,16,19H,5-7,10-12H2/t16-,19-/s2
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 45n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human ROMK expressed in CHO cells after 6 mins at -70 mV holding potential by electrophysiology method


Bioorg Med Chem Lett 26: 5695-5702 (2016)


Article DOI: 10.1016/j.bmcl.2016.10.064
BindingDB Entry DOI: 10.7270/Q2F191PS
More data for this
Ligand-Target Pair