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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Acetylcholinesterase' and Ligand = 'BDBM50252271'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Acetylcholinesterase


(Anopheles gambiae)
BDBM50252271
PNG
(CHEMBL4095547)
Show SMILES COc1cc(NC(=S)NCCN2CCOCC2)ccc1Cl
Show InChI InChI=1S/C14H20ClN3O2S/c1-19-13-10-11(2-3-12(13)15)17-14(21)16-4-5-18-6-8-20-9-7-18/h2-3,10H,4-9H2,1H3,(H2,16,17,21)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>2.00E+5n/an/an/an/an/an/a



Ume£ University

Curated by ChEMBL


Assay Description
Inhibition of AChE1 in Anopheles gambiae body extract using acetylthiocholine iodide as substrate measured over 60 secs by Ellman's method


Eur J Med Chem 134: 415-427 (2017)


Article DOI: 10.1016/j.ejmech.2017.03.050
BindingDB Entry DOI: 10.7270/Q23X893Z
More data for this
Ligand-Target Pair
Acetylcholinesterase


(Homo sapiens (Human))
BDBM50252271
PNG
(CHEMBL4095547)
Show SMILES COc1cc(NC(=S)NCCN2CCOCC2)ccc1Cl
Show InChI InChI=1S/C14H20ClN3O2S/c1-19-13-10-11(2-3-12(13)15)17-14(21)16-4-5-18-6-8-20-9-7-18/h2-3,10H,4-9H2,1H3,(H2,16,17,21)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>2.00E+5n/an/an/an/an/an/a



Ume£ University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human AChE expressed in HEK293F cells using acetylthiocholine iodide as substrate measured over 60 secs by Ellman's method


Eur J Med Chem 134: 415-427 (2017)


Article DOI: 10.1016/j.ejmech.2017.03.050
BindingDB Entry DOI: 10.7270/Q23X893Z
More data for this
Ligand-Target Pair