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BDBM50007234 7-Fluoro-1,3-dihydro-imidazo[4,5-b]quinolin-2-one::CHEMBL323071

SMILES: Fc1ccc2nc3[nH]c(=O)[nH]c3cc2c1

InChI Key: InChIKey=XTXHKKBSLRGOJD-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50007234   
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
Phosphodiesterase 3


(Homo sapiens (Human))
BDBM50007234
PNG
(7-Fluoro-1,3-dihydro-imidazo[4,5-b]quinolin-2-one ...)
Show SMILES Fc1ccc2nc3[nH]c(=O)[nH]c3cc2c1
Show InChI InChI=1S/C10H6FN3O/c11-6-1-2-7-5(3-6)4-8-9(12-7)14-10(15)13-8/h1-4H,(H2,12,13,14,15)
PDB
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 300n/an/an/an/an/an/a



Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibition of hydrolysis of c-AMP phosphodiesterase in human platelets


J Med Chem 34: 2906-16 (1991)


BindingDB Entry DOI: 10.7270/Q20P0Z03
More data for this
Ligand-Target Pair
Homo sapiens phosphodiesterase 2A (PDE2A)


(Homo sapiens (Human))
BDBM50007234
PNG
(7-Fluoro-1,3-dihydro-imidazo[4,5-b]quinolin-2-one ...)
Show SMILES Fc1ccc2nc3[nH]c(=O)[nH]c3cc2c1
Show InChI InChI=1S/C10H6FN3O/c11-6-1-2-7-5(3-6)4-8-9(12-7)14-10(15)13-8/h1-4H,(H2,12,13,14,15)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL


Assay Description
Inhibition of cGMP hydrolysis by human platelet phosphodiesterase


J Med Chem 34: 2906-16 (1991)


BindingDB Entry DOI: 10.7270/Q20P0Z03
More data for this
Ligand-Target Pair