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SMILES: Oc1ccc(-c2nnc(s2)-c2ccccc2Br)c(O)c1

InChI Key: InChIKey=ABEOGPVWBZTVJD-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 2 hits for monomerid = 50429786   
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))
BDBM50429786
PNG
(CHEMBL396226)
Show SMILES Oc1ccc(-c2nnc(s2)-c2ccccc2Br)c(O)c1
Show InChI InChI=1S/C14H9BrN2O2S/c15-11-4-2-1-3-9(11)13-16-17-14(20-13)10-6-5-8(18)7-12(10)19/h1-7,18-19H
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 290n/an/an/an/an/an/a



University of Life Sciences

Curated by ChEMBL


Assay Description
Inhibition of equine serum BChE using butylthiocholine iodide as substrate after 10 mins by Ellman method


Eur J Med Chem 62: 311-9 (2013)


Article DOI: 10.1016/j.ejmech.2012.12.060
BindingDB Entry DOI: 10.7270/Q27S7Q4V
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50429786
PNG
(CHEMBL396226)
Show SMILES Oc1ccc(-c2nnc(s2)-c2ccccc2Br)c(O)c1
Show InChI InChI=1S/C14H9BrN2O2S/c15-11-4-2-1-3-9(11)13-16-17-14(20-13)10-6-5-8(18)7-12(10)19/h1-7,18-19H
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 60n/an/an/an/an/an/a



University of Life Sciences

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE using acetylcholine iodide as substrate after 10 mins by Ellman method


Eur J Med Chem 62: 311-9 (2013)


Article DOI: 10.1016/j.ejmech.2012.12.060
BindingDB Entry DOI: 10.7270/Q27S7Q4V
More data for this
Ligand-Target Pair