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SMILES: Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)[N+]([O-])=O)nn1

InChI Key: InChIKey=XAIBXYLSSYRDSH-UHFFFAOYSA-N

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

Found 2 hits for monomerid = 50536288   
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
Acetylcholinesterase


(Electrophorus electricus (Electric eel))
BDBM50536288
PNG
(CHEMBL4561751)
Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)[N+]([O-])=O)nn1
Show InChI InChI=1S/C23H26N6O4/c1-17-2-5-19(14-21(17)23(30)24-8-9-27-10-12-33-13-11-27)22-16-28(26-25-22)15-18-3-6-20(7-4-18)29(31)32/h2-7,14,16H,8-13,15H2,1H3,(H,24,30)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2.05E+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
Cholinesterase


(Equus caballus (Horse))
BDBM50536288
PNG
(CHEMBL4561751)
Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)[N+]([O-])=O)nn1
Show InChI InChI=1S/C23H26N6O4/c1-17-2-5-19(14-21(17)23(30)24-8-9-27-10-12-33-13-11-27)22-16-28(26-25-22)15-18-3-6-20(7-4-18)29(31)32/h2-7,14,16H,8-13,15H2,1H3,(H,24,30)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.05E+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