Compile Data Set for Download or QSAR
Report error Found 32 Enz. Inhib. hit(s) with all data for entry = 50042967
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433917BDBM50433917(CHEMBL2380611)
Affinity DataIC50: 3.90nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433925BDBM50433925(CHEMBL2380603)
Affinity DataIC50: 7.60nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433918BDBM50433918(CHEMBL2380610)
Affinity DataIC50: 7.70nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433922BDBM50433922(CHEMBL2380606)
Affinity DataIC50: 7.90nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433921BDBM50433921(CHEMBL2380607)
Affinity DataIC50: 8.10nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433924BDBM50433924(CHEMBL2380604)
Affinity DataIC50: 8.10nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433923BDBM50433923(CHEMBL2380605)
Affinity DataIC50: 8.60nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433928BDBM50433928(CHEMBL2380615)
Affinity DataIC50: 9.90nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433926BDBM50433926(CHEMBL2380602)
Affinity DataIC50: 10nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433927BDBM50433927(CHEMBL2380601)
Affinity DataIC50: 10nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433919BDBM50433919(CHEMBL2380609)
Affinity DataIC50: 11nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433929BDBM50433929(CHEMBL2380614)
Affinity DataIC50: 11nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 8961BDBM8961(CHEMBL95 | Cognex | cid_1935 | CHEMBL1337960 | 1,2...)
Affinity DataIC50: 11nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433920BDBM50433920(CHEMBL2380608)
Affinity DataIC50: 14nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433930BDBM50433930(CHEMBL2380613)
Affinity DataIC50: 14nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433931BDBM50433931(CHEMBL2380612)
Affinity DataIC50: 59nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 8961BDBM8961(CHEMBL95 | Cognex | cid_1935 | CHEMBL1337960 | 1,2...)
Affinity DataIC50: 70nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433924BDBM50433924(CHEMBL2380604)
Affinity DataIC50: 112nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433928BDBM50433928(CHEMBL2380615)
Affinity DataIC50: 183nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433923BDBM50433923(CHEMBL2380605)
Affinity DataIC50: 189nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433929BDBM50433929(CHEMBL2380614)
Affinity DataIC50: 193nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433920BDBM50433920(CHEMBL2380608)
Affinity DataIC50: 227nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433919BDBM50433919(CHEMBL2380609)
Affinity DataIC50: 261nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433927BDBM50433927(CHEMBL2380601)
Affinity DataIC50: 341nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433930BDBM50433930(CHEMBL2380613)
Affinity DataIC50: 345nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433922BDBM50433922(CHEMBL2380606)
Affinity DataIC50: 357nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433918BDBM50433918(CHEMBL2380610)
Affinity DataIC50: 641nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433931BDBM50433931(CHEMBL2380612)
Affinity DataIC50: 715nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433921BDBM50433921(CHEMBL2380607)
Affinity DataIC50: 1.01E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433926BDBM50433926(CHEMBL2380602)
Affinity DataIC50: 1.35E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433917BDBM50433917(CHEMBL2380611)
Affinity DataIC50: 1.46E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50433925BDBM50433925(CHEMBL2380603)
Affinity DataIC50: 4.31E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed