Compile Data Set for Download or QSAR
Found 97 with Last Name = 'brown' and Initial = 'ce'
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442776(CHEMBL2443348)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442766(CHEMBL2443358)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360383(CHEMBL1933700)copy SMILEScopy InChI
Affinity DataKi:  50nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360381(CHEMBL1933694)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442767(CHEMBL2443357)copy SMILEScopy InChI
Affinity DataKi:  70nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360382(CHEMBL1933699)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442777(CHEMBL2443365)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442770(CHEMBL2443354)copy SMILEScopy InChI
Affinity DataKi:  90nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360380(CHEMBL1933693)copy SMILEScopy InChI
Affinity DataKi:  100nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442771(CHEMBL2443353)copy SMILEScopy InChI
Affinity DataKi:  110nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442775(CHEMBL2443349)copy SMILEScopy InChI
Affinity DataKi:  111nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442764(CHEMBL2443360)copy SMILEScopy InChI
Affinity DataKi:  130nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033887(CHEMBL3358611)copy SMILEScopy InChI
Affinity DataKi:  146nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442768(CHEMBL2443356)copy SMILEScopy InChI
Affinity DataKi:  160nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442773(CHEMBL2443351)copy SMILEScopy InChI
Affinity DataKi:  170nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442765(CHEMBL2443359)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442769(CHEMBL2443355)copy SMILEScopy InChI
Affinity DataKi:  237nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360384(CHEMBL1933701)copy SMILEScopy InChI
Affinity DataKi:  250nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442774(CHEMBL2443350)copy SMILEScopy InChI
Affinity DataKi:  330nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442762(CHEMBL2443362)copy SMILEScopy InChI
Affinity DataKi:  350nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)copy SMILEScopy InChI
Affinity DataKi:  398nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442761(CHEMBL2443364)copy SMILEScopy InChI
Affinity DataKi:  647nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360378(CHEMBL1933690)copy SMILEScopy InChI
Affinity DataKi:  790nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442772(CHEMBL2443352)copy SMILEScopy InChI
Affinity DataKi:  820nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50442763(CHEMBL2443361)copy SMILEScopy InChI
Affinity DataKi:  841nMAssay Description:Inhibition of recombinant human aromatase using O-dibenzylfluorescein benzyl ester as substrate by fluorometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QJ7JQBPubMed
TargetAromatase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360379(CHEMBL1933692)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of human recombinant aromatase assessed as conversion of O-dibenzylfluorescein benzyl ester substrate to fluorescein byproduct by fluorome...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033944(CHEMBL3358598)copy SMILEScopy InChI
Affinity DataKi:  4.77E+3nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetCytochrome P450 1A1(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360379(CHEMBL1933692)copy SMILEScopy InChI
Affinity DataKi:  5.37E+3nMAssay Description:Inhibition of CYP1A1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033946(CHEMBL3358596)copy SMILEScopy InChI
Affinity DataKi:  6.62E+3nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033888(CHEMBL3358610)copy SMILEScopy InChI
Affinity DataKi:  1.15E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033890(CHEMBL3358608)copy SMILEScopy InChI
Affinity DataKi:  1.24E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetCytochrome P450 1A1(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50360380(CHEMBL1933693)copy SMILEScopy InChI
Affinity DataKi:  3.09E+4nMAssay Description:Inhibition of CYP1A1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6KS2PubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033943(CHEMBL3358599)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033940(CHEMBL3358600)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033939(CHEMBL3358601)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033897(CHEMBL3358602)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033896(CHEMBL3358603)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033895(CHEMBL3358604)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033893(CHEMBL3358605)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033892(CHEMBL3358606)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033891(CHEMBL3358607)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033889(CHEMBL3358609)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033945(CHEMBL3358597)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033947(CHEMBL3358595)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033963(CHEMBL3358594)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50033993(CHEMBL3358593)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50034005(CHEMBL3358592)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50034006(CHEMBL3358591)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
TargetSignal transducer and activator of transcription 5B(Homo sapiens (Human))
University of Toronto Mississauga

Curated by ChEMBL
LigandPNGBDBM50034007(CHEMBL3358590)copy SMILEScopy InChI
Affinity DataKi: >6.00E+4nMAssay Description:Inhibition of STAT5B SH2 domain (unknown origin)-5-FAM-GpYLVLDKW interaction compound treated for 15 mins by fluorescent polarization assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25X2BJJPubMed
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