BDBM2689 3-[1-(3-dymethylaminopropyl)-indol-3-yl]-4-(indol-3-yl)-3-pyrrolin-2-one::3-{1-[3-(dimethylamino)propyl]-1H-indol-3-yl}-4-(1H-indol-3-yl)-2,5-dihydro-1H-pyrrol-2-one::Bisindolyl deriv. 17

SMILES CN(C)CCCn1cc(C2=C(CNC2=O)c2c[nH]c3ccccc23)c2ccccc12

InChI Key InChIKey=HJPXCQGPIFXKKR-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 2689   

LigandPNGBDBM2689(3-[1-(3-dymethylaminopropyl)-indol-3-yl]-4-(indol-...)
Affinity DataIC50: 2.75E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/22/2004
Entry Details
PubMed
LigandPNGBDBM2689(3-[1-(3-dymethylaminopropyl)-indol-3-yl]-4-(indol-...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/22/2004
Entry Details
PubMed
LigandPNGBDBM2689(3-[1-(3-dymethylaminopropyl)-indol-3-yl]-4-(indol-...)
Affinity DataIC50: 2.75E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/22/2004
Entry Details
PubMed