BindingDB logo
myBDB logout

BDBM50360974 CHEMBL1935426

SMILES: O=S1(=O)CCC(COc2ccc3OC4(CCN(CC4)C4CCC4)CCc3c2)CC1

InChI Key: InChIKey=BITWXVYTBYRISR-UHFFFAOYSA-N

Data: 5 KI  2 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 = 50360974   
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
Potassium voltage-gated channel subfamily H member 2


(Human)
BDBM50360974
PNG
(CHEMBL1935426)
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)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
n/an/a 1.10E+4n/an/an/an/an/an/a


TBA



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


(Human)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
4n/an/an/an/an/an/an/an/a


TBA



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


(Rat)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
9n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Histamine H1 receptor


(Human)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
>1.00E+4n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Histamine H2 receptor


(Human)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
>1.00E+4n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Histamine H4 receptor


(Human)
BDBM50360974
PNG
(CHEMBL1935426)
GoogleScholar
UniChem
>1.00E+4n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair