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SMILES: [Br-].C(C[n+]1cc2ccccc2c2ccccc12)c1ccccc1

InChI Key: InChIKey=QDRIDOYDSLXOIK-UHFFFAOYSA-M

Find this compound or compounds like it in BindingDB or PDB:
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50016828   
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


(Equus caballus (Horse))
BDBM50016828
PNG
(CHEMBL3276418)
Show SMILES [Br-].C(C[n+]1cc2ccccc2c2ccccc12)c1ccccc1
Show InChI InChI=1S/C21H18N.BrH/c1-2-8-17(9-3-1)14-15-22-16-18-10-4-5-11-19(18)20-12-6-7-13-21(20)22;/h1-13,16H,14-15H2;1H/q+1;/p-1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
54n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Reversible mixed-type inhibition of horse serum butyrylcholinesterase using acetylcholine bromide as substrate assessed as free enzyme-inhibitor comp...


J Med Chem 20: 1617-23 (1978)


BindingDB Entry DOI: 10.7270/Q29025BQ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50016828
PNG
(CHEMBL3276418)
Show SMILES [Br-].C(C[n+]1cc2ccccc2c2ccccc12)c1ccccc1
Show InChI InChI=1S/C21H18N.BrH/c1-2-8-17(9-3-1)14-15-22-16-18-10-4-5-11-19(18)20-12-6-7-13-21(20)22;/h1-13,16H,14-15H2;1H/q+1;/p-1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
280n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Reversible mixed-type inhibition of electric eel acetylcholinesterase using acetylcholine bromide as substrate assessed as free enzyme-inhibitor comp...


J Med Chem 20: 1617-23 (1978)


BindingDB Entry DOI: 10.7270/Q29025BQ
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Equus caballus (Horse))
BDBM50016828
PNG
(CHEMBL3276418)
Show SMILES [Br-].C(C[n+]1cc2ccccc2c2ccccc12)c1ccccc1
Show InChI InChI=1S/C21H18N.BrH/c1-2-8-17(9-3-1)14-15-22-16-18-10-4-5-11-19(18)20-12-6-7-13-21(20)22;/h1-13,16H,14-15H2;1H/q+1;/p-1
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
310n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Reversible mixed-type inhibition of horse serum butyrylcholinesterase using acetylcholine bromide as substrate by Lineweaver-Burk plot analysis


J Med Chem 20: 1617-23 (1978)


BindingDB Entry DOI: 10.7270/Q29025BQ
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50016828
PNG
(CHEMBL3276418)
Show SMILES [Br-].C(C[n+]1cc2ccccc2c2ccccc12)c1ccccc1
Show InChI InChI=1S/C21H18N.BrH/c1-2-8-17(9-3-1)14-15-22-16-18-10-4-5-11-19(18)20-12-6-7-13-21(20)22;/h1-13,16H,14-15H2;1H/q+1;/p-1
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
780n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Reversible mixed-type inhibition of electric eel acetylcholinesterase using acetylcholine bromide as substrate by Lineweaver-Burk plot analysis


J Med Chem 20: 1617-23 (1978)


BindingDB Entry DOI: 10.7270/Q29025BQ
More data for this
Ligand-Target Pair