BDBM50145371 2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinoline-7-carboxylic acid::2-(2,4-dihydroxybenzylcarbamoyl)-8-hydroxyquinoline-7-carboxylic acid::CHEMBL81714

SMILES OC(=O)c1ccc2ccc(nc2c1O)C(=O)NCc1ccc(O)cc1O

InChI Key InChIKey=XCUIQBHAIMNBMZ-UHFFFAOYSA-N

Data  9 IC50

  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 9 hits for monomerid = 50145371   

TargetIntegrase(Human immunodeficiency virus type 1)
Cnrs Umr 8076

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 5.00E+3nMAssay Description:In vitro inhibition of recombinant integrase activity in a standard 3'-processing assay.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCyclin-dependent kinase 5 activator 1(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CDK5/P25More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CDK1/cyclin BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetGlycogen synthase kinase-3(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of GSK3alpha/betaMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetSerine/threonine-protein kinase pim-1(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 200nMAssay Description:Inhibition of PIM1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetCasein kinase I isoform alpha(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CK1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 4.50E+3nMAssay Description:Inhibition of mouse DYRK1A expressed in Escherichia coli after 20 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 2(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibition of DYRK2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetDual specificity protein kinase CLK1(Human)
Paris-Sud University

Curated by ChEMBL
LigandPNGBDBM50145371(2-(2,4-Dihydroxy-benzylcarbamoyl)-8-hydroxy-quinol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of CLK1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed