Compile Data Set for Download or QSAR
Report error Found 78 Enz. Inhib. hit(s) with all data for entry = 50048976
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 11682BDBM11682(2,3-dihydroxybutanedioic acid; 3-[(1S)-1-(dimethyl...)
Affinity DataIC50: 260nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232245BDBM50232245(CHEMBL4080105)
Affinity DataKi:  480nMAssay Description:Competitive inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate by Michaelis-Menten plot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232245BDBM50232245(CHEMBL4080105)
Affinity DataIC50: 710nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232245BDBM50232245(CHEMBL4080105)
Affinity DataKi:  920nMAssay Description:Noncompetitive inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate by Michaelis-Menten plot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232315BDBM50232315(CHEMBL4072258)
Affinity DataIC50: 1.11E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232310BDBM50232310(CHEMBL4105158)
Affinity DataIC50: 1.36E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232311BDBM50232311(CHEMBL4087978)
Affinity DataIC50: 1.56E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232226BDBM50232226(CHEMBL4094981)
Affinity DataIC50: 1.83E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232229BDBM50232229(CHEMBL4072405)
Affinity DataIC50: 1.94E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232315BDBM50232315(CHEMBL4072258)
Affinity DataIC50: 2.23E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232236BDBM50232236(CHEMBL4095695)
Affinity DataIC50: 2.34E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232247BDBM50232247(CHEMBL4094761)
Affinity DataIC50: 2.65E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232231BDBM50232231(CHEMBL4099340)
Affinity DataIC50: 2.67E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232304BDBM50232304(CHEMBL4100736)
Affinity DataIC50: 2.91E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232305BDBM50232305(CHEMBL4082739)
Affinity DataIC50: 2.99E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232234BDBM50232234(CHEMBL4059684)
Affinity DataIC50: 3.18E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232302BDBM50232302(CHEMBL4063663)
Affinity DataIC50: 3.83E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232310BDBM50232310(CHEMBL4105158)
Affinity DataIC50: 3.98E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232304BDBM50232304(CHEMBL4100736)
Affinity DataIC50: 4.03E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232246BDBM50232246(CHEMBL4098132)
Affinity DataIC50: 4.12E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232303BDBM50232303(CHEMBL4093019)
Affinity DataIC50: 4.78E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232243BDBM50232243(CHEMBL4068340)
Affinity DataIC50: 4.78E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232244BDBM50232244(CHEMBL4090413)
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232313BDBM50232313(CHEMBL4074258)
Affinity DataIC50: 4.84E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232226BDBM50232226(CHEMBL4094981)
Affinity DataIC50: 4.86E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232306BDBM50232306(CHEMBL4062593)
Affinity DataIC50: 5.05E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232246BDBM50232246(CHEMBL4098132)
Affinity DataIC50: 5.45E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232312BDBM50232312(CHEMBL4069385)
Affinity DataIC50: 5.69E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232244BDBM50232244(CHEMBL4090413)
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232303BDBM50232303(CHEMBL4093019)
Affinity DataIC50: 6.21E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232220BDBM50232220(CHEMBL4063045)
Affinity DataIC50: 6.72E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232312BDBM50232312(CHEMBL4069385)
Affinity DataIC50: 7.14E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232220BDBM50232220(CHEMBL4063045)
Affinity DataIC50: 8.40E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232228BDBM50232228(CHEMBL4087300)
Affinity DataIC50: 8.47E+3nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232221BDBM50232221(CHEMBL4084714)
Affinity DataIC50: 8.95E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232309BDBM50232309(CHEMBL4086323)
Affinity DataIC50: 9.93E+3nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232221BDBM50232221(CHEMBL4084714)
Affinity DataIC50: 1.04E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 11682BDBM11682(2,3-dihydroxybutanedioic acid; 3-[(1S)-1-(dimethyl...)
Affinity DataIC50: 1.05E+4nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232313BDBM50232313(CHEMBL4074258)
Affinity DataIC50: 1.11E+4nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232229BDBM50232229(CHEMBL4072405)
Affinity DataIC50: 1.13E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232222BDBM50232222(CHEMBL4064846)
Affinity DataIC50: 1.14E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232219BDBM50232219(CHEMBL4103604)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232314BDBM50232314(CHEMBL4101703)
Affinity DataIC50: 1.26E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232245BDBM50232245(CHEMBL4080105)
Affinity DataIC50: 1.29E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232311BDBM50232311(CHEMBL4087978)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232305BDBM50232305(CHEMBL4082739)
Affinity DataIC50: 1.35E+4nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232301BDBM50232301(CHEMBL4085283)
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232243BDBM50232243(CHEMBL4068340)
Affinity DataIC50: 1.44E+4nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232228BDBM50232228(CHEMBL4087300)
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) using acetylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
TargetCholinesterase(Human)
Hu'Nan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50232223BDBM50232223(CHEMBL4078463)
Affinity DataIC50: 1.68E+4nMAssay Description:Inhibition of butyrylcholinesterase (unknown origin) using butyrylthiocholine iodide as substrate after 25 mins by Ellmann methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/11/2019
Entry Details Article
PubMed
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