Compile Data Set for Download or QSAR
Found 507 with Last Name = 'balint' and Initial = 'j'
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520160(CHEMBL4515413 | US10894784, Example 01.03)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged FLT3 (564 to end residues) expressed in sf21 cells using biotin labelled Ahx-GGEEEEYFELVKKKK pe...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520150(CHEMBL4566796)copy SMILEScopy InChI
Affinity DataIC50: 0.700nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520175(CHEMBL4451595 | US10894784, Example 135.02)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged FLT3 (564 to end residues) expressed in sf21 cells using biotin labelled Ahx-GGEEEEYFELVKKKK pe...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520142(CHEMBL4435393)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520159(CHEMBL4543618)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged FLT3 (564 to end residues) expressed in sf21 cells using biotin labelled Ahx-GGEEEEYFELVKKKK pe...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520151(CHEMBL4537673)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520150(CHEMBL4566796)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520151(CHEMBL4537673)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520159(CHEMBL4543618)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520157(CHEMBL4436188)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520148(CHEMBL4538751 | US10894784, Example 30.03.01.A)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520165(CHEMBL4454902)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367317(Methyl (6RS)-4-oxo-3-(phenylamino)-2-(pyridin-4-yl...)copy SMILES
Affinity DataIC50: 3nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367598(US10227299, Example 288)copy SMILES
Affinity DataIC50: 3nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520157(CHEMBL4436188)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520148(CHEMBL4538751 | US10894784, Example 30.03.01.A)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520165(CHEMBL4454902)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367372((6RS)-6-[(Ethylsulfanyl)methyl]-3-(phenylamino)-2-...)copy SMILES
Affinity DataIC50: 4nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367367(N-Methyl-4-oxo-3-(phenylamino)-N-propyl-2-(pyridin...)copy SMILES
Affinity DataIC50: 4nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367368(N,N-Dimethyl-4-oxo-3-(phenylamino)-2-(pyridin-4-yl...)copy SMILES
Affinity DataIC50: 4nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367593(US10227299, Example 283)copy SMILES
Affinity DataIC50: 4nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520150(CHEMBL4566796)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged FLT3 (564 to end residues) expressed in sf21 cells using biotin labelled Ahx-GGEEEEYFELVKKKK pe...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520161(CHEMBL4468020 | US10894784, Example 39.01.02)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520165(CHEMBL4454902)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetCyclin-T1/Cyclin-dependent kinase 9(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520145(CHEMBL4459120)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of recombinant full length human His-tagged CDK9/CyclinT1 expressed in baculovirus expression system using biotin-labelled Ttds-YISPLKSPYK...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367590(US10227299, Example 280)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367371((6RS)-3-(Phenylamino)-6-[(propan-2-ylsulfanyl)meth...)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367472(Methyl (6RS)-2-[3-(2-methoxyethoxy)pyridin-4-yl]-4...)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367507((6RS)-2-2-[(4-Fluorobenzoyl)amino]pyridin-4-yl-N,N...)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367412((6RS)—N-Methyl-N-(2-methylpropyl)-4-oxo-3-(ph...)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367349((6RS)-6-Ethenyl-3-(phenylamino)-2-(pyridin-4-yl)-1...)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367592(US10227299, Example 282)copy SMILES
Affinity DataIC50: 5nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520142(CHEMBL4435393)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520152(CHEMBL4594167 | US10894784, Example 150.02)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of recombinant human N-terminal GST-tagged FLT3 (564 to end residues) expressed in sf21 cells using biotin labelled Ahx-GGEEEEYFELVKKKK pe...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367391((6RS)-6-[(Ethylsulfonyl)methyl]-3-(phenylamino)-2-...)copy SMILES
Affinity DataIC50: 6nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367454(Methyl (6RS)-2-2-[(4-fluorobenzoyl)amino]pyridin-4...)copy SMILES
Affinity DataIC50: 6nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520157(CHEMBL4436188)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520150(CHEMBL4566796)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of recombinant full length human N-terminal His-tagged TBK1 using biotin-labelled Ahx-GDEDFSSFAEPG peptide as substrate preincubated with ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367357(N-[(6RS)-4-Oxo-3-(phenylamino)-2-(pyridin-4-yl)-4,...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Homo sapiens (Human))
Bayer AG

Curated by ChEMBL
LigandPNGBDBM50520161(CHEMBL4468020 | US10894784, Example 39.01.02)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of recombinant full length human C-terminal GST-tagged IKKepsilon expressed in baculovirus expression system using biotin-labelled Ahx-GDE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7795PubMed
LigandPNGBDBM367595(US10227299, Example 285)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367597(US10227299, Example 287)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367455(Methyl (6RS)-4-oxo-3-(phenylamino)-2-2-[(1,3-thiaz...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367463(N-4-[(6RS)-6-(Azidomethyl)-4-oxo-3-(phenylamino)-4...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367469(Methyl (6RS)-3-anilino-2-[3-(cyclopropylmethoxy)py...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367509((6RS)—N,N-Dimethyl-4-oxo-3-(phenylamino)-2-2-...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367515((6RS)-3-Anilino-N,N-dlisopropyl-4-oxo-2-(pyridin-4...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367384(N-(2-Hydroxyethyl)-N-methyl-4-oxo-3-(phenylamino)-...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367386((6RS)-2-(3-Fluoropyridin-4-yl)-N,N-dimethyl-4-oxo-...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
LigandPNGBDBM367432((6RS)—N,N-Diethyl-4-oxo-3-(phenylamino)-2-(py...)copy SMILES
Affinity DataIC50: 7nMAssay Description:Bub1-inhibitory activities of compounds described in the present invention were quantified using a time-resolved fluorescence energy transfer (TR-FRE...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QN6931US Patent
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