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BDBM50379611 CHEMBL2013045

SMILES: CS(=O)(=O)N1CCC(CC1)Oc1ccc2OC3(CCN(CC3)C3CCC3)CCc2c1

InChI Key: InChIKey=BFKPZXXQVYWHKU-UHFFFAOYSA-N

Data: 2 KI  5 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50379611   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Cytochrome P450 1A2


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Histamine H3 receptor


(Human)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
7n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Histamine H3 receptor


(Rat)
BDBM50379611
PNG
(CHEMBL2013045)
GoogleScholar
UniChem
17n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair