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BDBM50397913 CHEMBL2179516

SMILES: Cc1ncoc1C(=O)N1CC2CNCC2C1

InChI Key: InChIKey=ILRKKMGSYJDPCB-UHFFFAOYSA-N

Data: 5 KI  1 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 6 hits for monomerid = 50397913   
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))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
PDB
MMDB

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PC cid
PC sid
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Article
PubMed
8n/an/an/an/an/an/an/an/a



Targacept, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]nicotine from alpha4beta2 nAChR in human SH-EP1 cells after 2 hrs by liquid scintillation assay


J Med Chem 55: 9181-94 (2012)


Article DOI: 10.1021/jm3006542
BindingDB Entry DOI: 10.7270/Q2W0972W
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor subunit alpha-4


(Homo sapiens (Human))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
PDB

KEGG

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antibodypedia
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US Patent
9.20 -10.8n/an/an/an/an/an/a21



Targacept, Inc.

US Patent


Assay Description
The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=...


US Patent US8921410 (2014)


BindingDB Entry DOI: 10.7270/Q2QZ28PT
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor


(Rattus norvegicus (Rat))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
PDB

KEGG

UniProtKB/SwissProt

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PC sid
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US Patent
15 -10.5n/an/an/an/an/an/a21



Targacept, Inc.

US Patent


Assay Description
The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=...


US Patent US8921410 (2014)


BindingDB Entry DOI: 10.7270/Q2QZ28PT
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor protein alpha-7 subunit


(Homo sapiens (Human))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
PDB

KEGG

UniProtKB/SwissProt

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

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Article
PubMed
5.90E+3n/an/an/an/an/an/an/an/a



Targacept, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]epibatidine from human alpha7 nAChR expressed in CHO cells after 2 hrs by liquid scintillation counting


J Med Chem 55: 9181-94 (2012)


Article DOI: 10.1021/jm3006542
BindingDB Entry DOI: 10.7270/Q2W0972W
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor


(Rattus norvegicus (Rat))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
PDB

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UniChem

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US Patent
2.10E+5 -4.95n/an/an/an/an/an/a21



Targacept, Inc.

US Patent


Assay Description
The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=...


US Patent US8921410 (2014)


BindingDB Entry DOI: 10.7270/Q2QZ28PT
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50397913
PNG
(CHEMBL2179516)
Show SMILES Cc1ncoc1C(=O)N1CC2CNCC2C1
Show InChI InChI=1S/C11H15N3O2/c1-7-10(16-6-13-7)11(15)14-4-8-2-12-3-9(8)5-14/h6,8-9,12H,2-5H2,1H3
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 6.80E+3n/an/an/an/a



Targacept, Inc.

Curated by ChEMBL


Assay Description
Agonist activity at alpha4beta2 nAChR in human SH-EP1 cells assessed as calcium flux by calcium4-based FLIPR assay


J Med Chem 55: 9181-94 (2012)


Article DOI: 10.1021/jm3006542
BindingDB Entry DOI: 10.7270/Q2W0972W
More data for this
Ligand-Target Pair