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BDBM50388679 CHEMBL2059315

SMILES: O=C1COc2ccccc2N1CCCN1CCC(CC1)n1c2ccncc2[nH]c1=O

InChI Key: InChIKey=PIZNIEUZHRJIAB-UHFFFAOYSA-N

Data: 1 KI  1 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 2 hits for monomerid = 50388679   
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
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50388679
PNG
(CHEMBL2059315)
Show SMILES O=C1COc2ccccc2N1CCCN1CCC(CC1)n1c2ccncc2[nH]c1=O
Show InChI InChI=1S/C22H25N5O3/c28-21-15-30-20-5-2-1-4-19(20)26(21)11-3-10-25-12-7-16(8-13-25)27-18-6-9-23-14-17(18)24-22(27)29/h1-2,4-6,9,14,16H,3,7-8,10-13,15H2,(H,24,29)
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PC cid
PC sid
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Similars

Article
PubMed
1.35E+3n/an/an/an/an/an/an/an/a



H. Lundbeck A/S

Curated by ChEMBL


Assay Description
Displacement of [3H]raclopride from human D2L receptor expressed in CHO cells after 60 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5134-40 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.048
BindingDB Entry DOI: 10.7270/Q24M95MM
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50388679
PNG
(CHEMBL2059315)
Show SMILES O=C1COc2ccccc2N1CCCN1CCC(CC1)n1c2ccncc2[nH]c1=O
Show InChI InChI=1S/C22H25N5O3/c28-21-15-30-20-5-2-1-4-19(20)26(21)11-3-10-25-12-7-16(8-13-25)27-18-6-9-23-14-17(18)24-22(27)29/h1-2,4-6,9,14,16H,3,7-8,10-13,15H2,(H,24,29)
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antibodypedia
GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 4.60E+4n/an/an/an/an/an/a



H. Lundbeck A/S

Curated by ChEMBL


Assay Description
Inhibition of human ERG expressed in CHO cells after 30 mins by Rb+ flux assay


Bioorg Med Chem Lett 22: 5134-40 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.048
BindingDB Entry DOI: 10.7270/Q24M95MM
More data for this
Ligand-Target Pair