null

SMILES Fc1ccc(-c2ccc(CSc3nnc(o3)-c3ccc4OCCOc4c3)cc2)c(c1)C#N

InChI Key InChIKey=WYYSOGMUPDEQEM-UHFFFAOYSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50389083   

TargetProtein kinase C alpha type(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant PKCalpha by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant CDK5/p35 by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant GSK-3 beta using Ulight-CFFKNIVTPRTPPPSQGK-amide substrate incubated for 90 mins by LANCE method relative to controlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64KW5PubMed
TargetGlycogen synthase kinase-3 alpha(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibition of human recombinant GSK-3 alpha using Ulight-CFFKNIVTPRTPPPSQGK-amide substrate incubated for 60 mins by LANCE method relative to controlMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K64KW5PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21Z48DSPubMed
TargetCasein kinase I isoform epsilon(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human recombinant CK1epsilon by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 185nMAssay Description:Inhibition of human recombinant GSK3beta using pIRS-1 as substrate preincubated for 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed
TargetGlycogen synthase kinase-3 alpha(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of human recombinant GSK3alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed
TargetGlycogen synthase kinase-3 alpha(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 230nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21Z48DSPubMed
TargetAurora kinase A(Homo sapiens (Human))
Technische Universit£t Darmstadt

Curated by ChEMBL
LigandPNGBDBM50389083(CHEMBL2064535)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human recombinant AurKA by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MG7QK0PubMed