BDBM50392999 CHEMBL2152545

SMILES CCCCCCCNC(=O)Oc1ccc2N(C)C3N(CCc4ccccc34)Cc2c1

InChI Key InChIKey=NRSCUZWEMZYPRV-UHFFFAOYSA-N

Data  1 KI  14 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 15 hits for monomerid = 50392999   

TargetCholinesterase(Equus caballus (Horse))
TBA

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataKi:  12.7nMAssay Description:Time dependent inhibition of equine serum BChE assessed as stability constants of inhibitor-enzyme complex using acetylthiocholine as substrate after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
TBA

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  60nMAssay Description:Inhibition of equine serum BChE using acetylthiocholine as substrate after 2 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  6.5nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human erythrocyte AChE at 10 uM using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition and...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human erythrocyte AChE at 10 uM using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition and...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  6.40nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition and measured afte...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  6.5nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine iodide as substrate incubated for 30 mins followed by substrate addition and measured after 2...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  6.40nMAssay Description:Inhibition of human serum BChE using butyrylthiocholine iodide as substrate incubated for 30 mins followed by substrate addition and measured after 2...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate incubated for 30 mins followed by substrate addition and measured after 2.5 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  3.80E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate incubated for 30 mins followed by substrate addition and measured after 2.5 mins...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  48nMAssay Description:Inhibition of human BChE using butyrylthiocholineiodide as substrate preincubated for 20 mins followed by substrate addition and measured every 30 se...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  50nMAssay Description:Inhibition of human BChE using butyrylthiocholineiodide as substrate preincubated for 20 mins followed by substrate addition and measured every 30 se...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  6.40nMAssay Description:Pseduo-irreversible inhibition of human BChE using butyrylthiocholineiodide as substrate preincubated for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Julius Maximilian University W£Rzburg

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  3.80E+3nMAssay Description:Pseudo-irreversible inhibition of human AChE using acetylthiocholineiodide as substrate preincubated for 30 mins followed by substrate addition and m...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetCholinesterase(Equus caballus (Horse))
TBA

Curated by ChEMBL
LigandPNGBDBM50392999(CHEMBL2152545)
Affinity DataIC50:  58.9nMAssay Description:Inhibition of equine serum BChE using acetylthiocholine as substrate after 2 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed