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BDBM50399419 CHEMBL2178337

SMILES: CCNC(=O)OCCc1cc(on1)-c1cncc(OC[C@@H]2CCCN2)c1

InChI Key: InChIKey=WYJACLVBUWRJLU-HNNXBMFYSA-N

Data: 1 IC50  2 EC50

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 3 hits for monomerid = 50399419   
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
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50399419
PNG
(CHEMBL2178337)
Show SMILES CCNC(=O)OCCc1cc(on1)-c1cncc(OC[C@@H]2CCCN2)c1 |r|
Show InChI InChI=1S/C18H24N4O4/c1-2-20-18(23)24-7-5-14-9-17(26-22-14)13-8-16(11-19-10-13)25-12-15-4-3-6-21-15/h8-11,15,21H,2-7,12H2,1H3,(H,20,23)/t15-/m0/s1
PDB
MMDB

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KEGG

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PC cid
PC sid
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Similars

Article
PubMed
n/an/a>100n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at human alpha4beta2 nAChR expressed in human SH-EP1 cells assessed as inhibition of 86Rb+ efflux preincubated for 10 mins by liq...


J Med Chem 55: 9998-10009 (2012)


Article DOI: 10.1021/jm301177j
BindingDB Entry DOI: 10.7270/Q2CJ8FM1
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50399419
PNG
(CHEMBL2178337)
Show SMILES CCNC(=O)OCCc1cc(on1)-c1cncc(OC[C@@H]2CCCN2)c1 |r|
Show InChI InChI=1S/C18H24N4O4/c1-2-20-18(23)24-7-5-14-9-17(26-22-14)13-8-16(11-19-10-13)25-12-15-4-3-6-21-15/h8-11,15,21H,2-7,12H2,1H3,(H,20,23)/t15-/m0/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/an/an/a>100n/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Agonist activity at human alpha4beta2 nAChR expressed in human SH-EP1 cells assessed as stimulation of 86Rb+ efflux preincubated for 10 mins by liqui...


J Med Chem 55: 9998-10009 (2012)


Article DOI: 10.1021/jm301177j
BindingDB Entry DOI: 10.7270/Q2CJ8FM1
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50399419
PNG
(CHEMBL2178337)
Show SMILES CCNC(=O)OCCc1cc(on1)-c1cncc(OC[C@@H]2CCCN2)c1 |r|
Show InChI InChI=1S/C18H24N4O4/c1-2-20-18(23)24-7-5-14-9-17(26-22-14)13-8-16(11-19-10-13)25-12-15-4-3-6-21-15/h8-11,15,21H,2-7,12H2,1H3,(H,20,23)/t15-/m0/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/an/an/a>100n/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Agonist activity at human alpha4beta2 nAChR expressed in human SH-EP1 cells assessed as stimulation of 86Rb+ efflux preincubated for 10 mins by liqui...


J Med Chem 55: 9998-10009 (2012)


Article DOI: 10.1021/jm301177j
BindingDB Entry DOI: 10.7270/Q2CJ8FM1
More data for this
Ligand-Target Pair