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SMILES: NCCCCNc1c2CCCCc2nc2ccccc12

InChI Key: InChIKey=IRDRWZMLBBBOJK-UHFFFAOYSA-N

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 4 hits for monomerid = 50377433   
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
Cholinesterase


(Equus caballus (Horse))
BDBM50377433
PNG
(CHEMBL258926)
Show SMILES NCCCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C17H23N3/c18-11-5-6-12-19-17-13-7-1-3-9-15(13)20-16-10-4-2-8-14(16)17/h1,3,7,9H,2,4-6,8,10-12,18H2,(H,19,20)
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PubMed
n/an/a 22.9n/an/an/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's method


J Med Chem 55: 4309-21 (2012)


Article DOI: 10.1021/jm300106z
BindingDB Entry DOI: 10.7270/Q21837N7
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50377433
PNG
(CHEMBL258926)
Show SMILES NCCCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C17H23N3/c18-11-5-6-12-19-17-13-7-1-3-9-15(13)20-16-10-4-2-8-14(16)17/h1,3,7,9H,2,4-6,8,10-12,18H2,(H,19,20)
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n/an/a 23.6n/an/an/an/an/an/a



Friedrich-Schiller-Universit£t Jena

Curated by ChEMBL


Assay Description
Inhibition of electric eel AchE by Ellman's assay


Bioorg Med Chem Lett 18: 2905-9 (2008)


Article DOI: 10.1016/j.bmcl.2008.03.073
BindingDB Entry DOI: 10.7270/Q2M909KN
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50377433
PNG
(CHEMBL258926)
Show SMILES NCCCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C17H23N3/c18-11-5-6-12-19-17-13-7-1-3-9-15(13)20-16-10-4-2-8-14(16)17/h1,3,7,9H,2,4-6,8,10-12,18H2,(H,19,20)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
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n/an/a 7.10n/an/an/an/an/an/a



Friedrich-Schiller-Universit£t Jena

Curated by ChEMBL


Assay Description
Inhibition of equine BChE by Ellman's assay


Bioorg Med Chem Lett 18: 2905-9 (2008)


Article DOI: 10.1016/j.bmcl.2008.03.073
BindingDB Entry DOI: 10.7270/Q2M909KN
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50377433
PNG
(CHEMBL258926)
Show SMILES NCCCCNc1c2CCCCc2nc2ccccc12
Show InChI InChI=1S/C17H23N3/c18-11-5-6-12-19-17-13-7-1-3-9-15(13)20-16-10-4-2-8-14(16)17/h1,3,7,9H,2,4-6,8,10-12,18H2,(H,19,20)
UniProtKB/SwissProt

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CHEMBL
PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 39.3n/an/an/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Inhibition of eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's method


J Med Chem 55: 4309-21 (2012)


Article DOI: 10.1021/jm300106z
BindingDB Entry DOI: 10.7270/Q21837N7
More data for this
Ligand-Target Pair