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SMILES: Clc1ccc2c(NCCCCCCNC3CCc4[nH]c(=O)ccc4C3)c3CCCCc3nc2c1

InChI Key:

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 = 50582082   
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
Carboxylic ester hydrolase


(Rattus norvegicus (rat))
BDBM50582082
PNG
(CHEMBL5084050)
Show SMILES Clc1ccc2c(NCCCCCCNC3CCc4[nH]c(=O)ccc4C3)c3CCCCc3nc2c1
Reactome pathway
KEGG

UniProtKB/TrEMBL

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 574n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of rat serum BChE using butyrylthiocholine iodide as substrate by Ellman's method


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113827
BindingDB Entry DOI: 10.7270/Q2222ZP7
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50582082
PNG
(CHEMBL5084050)
Show SMILES Clc1ccc2c(NCCCCCCNC3CCc4[nH]c(=O)ccc4C3)c3CCCCc3nc2c1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.16E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of hERG expressed in CHO-K1 cells assessed as reduction in thallium influx incubated for 30 minutes by FLIPR


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113827
BindingDB Entry DOI: 10.7270/Q2222ZP7
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Rattus norvegicus (rat))
BDBM50582082
PNG
(CHEMBL5084050)
Show SMILES Clc1ccc2c(NCCCCCCNC3CCc4[nH]c(=O)ccc4C3)c3CCCCc3nc2c1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of rat cortex AChE using acetylthiocholine iodide as substrate by Ellman's method


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113827
BindingDB Entry DOI: 10.7270/Q2222ZP7
More data for this
Ligand-Target Pair