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SMILES: Cc1cc(C)cc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1

InChI Key: InChIKey=WEDFGVTXHPXYPZ-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50536301   
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))
BDBM50536301
PNG
(CHEMBL4547644)
Show SMILES Cc1cc(C)cc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1
Show InChI InChI=1S/C25H31N5O2/c1-18-12-19(2)14-21(13-18)16-30-17-24(27-28-30)22-5-4-20(3)23(15-22)25(31)26-6-7-29-8-10-32-11-9-29/h4-5,12-15,17H,6-11,16H2,1-3H3,(H,26,31)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 5.62E+4n/an/an/an/an/an/a



University of Jinan

Curated by ChEMBL


Assay Description
Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method


Bioorg Med Chem Lett 26: 3881-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.07.017
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50536301
PNG
(CHEMBL4547644)
Show SMILES Cc1cc(C)cc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1
Show InChI InChI=1S/C25H31N5O2/c1-18-12-19(2)14-21(13-18)16-30-17-24(27-28-30)22-5-4-20(3)23(15-22)25(31)26-6-7-29-8-10-32-11-9-29/h4-5,12-15,17H,6-11,16H2,1-3H3,(H,26,31)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.42E+4n/an/an/an/an/an/a



University of Jinan

Curated by ChEMBL


Assay Description
Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method


Bioorg Med Chem Lett 26: 3881-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.07.017
More data for this
Ligand-Target Pair