BDBM50246606 CHEMBL4099486

SMILES COCCN(CC(=O)NC(C)C)C(=O)CCCCCn1ccnc1\C=N\O

InChI Key InChIKey=NKPBFOFMXJWMQV-UHFFFAOYSA-N

Data  1 IC50  2 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50246606   

TargetAcetylcholinesterase(Human)
Tno

Curated by ChEMBL
LigandPNGBDBM50246606(CHEMBL4099486)
Affinity DataKd:  1.47E+6nMAssay Description:Reactivation of cyclosarin inhibited human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated up to 60 mins followed by substr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/29/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Tno

Curated by ChEMBL
LigandPNGBDBM50246606(CHEMBL4099486)
Affinity DataKd:  3.85E+5nMAssay Description:Reactivation of sarin inhibited human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated up to 60 mins followed by substrate a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/29/2019
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Tno

Curated by ChEMBL
LigandPNGBDBM50246606(CHEMBL4099486)
Affinity DataIC50: 1.00E+6nMAssay Description:Reactivation of organophosphate inhibited human erythrocyte AChE assessed as organophosphate IC50 using acetylthiocholine iodide as substrate preincu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/29/2019
Entry Details Article
PubMed