Compile Data Set for Download or QSAR
Found 136 with Last Name = 'de castro vasconcelos goncalves' and Initial = 'mb'
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM323588(Retinoic Acid | US10188615, at-RA | US10752616, Co...)copy SMILEScopy InChI
Affinity DataEC50:  1.88nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM323588(Retinoic Acid | US10188615, at-RA | US10752616, Co...)copy SMILEScopy InChI
Affinity DataEC50:  1.20nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM323588(Retinoic Acid | US10188615, at-RA | US10752616, Co...)copy SMILEScopy InChI
Affinity DataEC50:  0.900nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526314(CHEMBL4459692 | US10752616, Code No. BHBA-001)copy SMILEScopy InChI
Affinity DataEC50:  1.94nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526314(CHEMBL4459692 | US10752616, Code No. BHBA-001)copy SMILEScopy InChI
Affinity DataEC50:  26nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526314(CHEMBL4459692 | US10752616, Code No. BHBA-001)copy SMILEScopy InChI
Affinity DataEC50:  11nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458121(US10752616, Code No. BHBA-002)copy SMILEScopy InChI
Affinity DataEC50:  11.4nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458121(US10752616, Code No. BHBA-002)copy SMILEScopy InChI
Affinity DataEC50:  136nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458121(US10752616, Code No. BHBA-002)copy SMILEScopy InChI
Affinity DataEC50:  29nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458124(US10752616, Code No. BHBA-003)copy SMILEScopy InChI
Affinity DataEC50:  16nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458124(US10752616, Code No. BHBA-003)copy SMILEScopy InChI
Affinity DataEC50:  160nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458124(US10752616, Code No. BHBA-003)copy SMILEScopy InChI
Affinity DataEC50:  36nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458127(US10752616, Code No. BHBA-004)copy SMILEScopy InChI
Affinity DataEC50:  10nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458133(US10752616, Code No. BHBA-005)copy SMILEScopy InChI
Affinity DataEC50:  23nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458133(US10752616, Code No. BHBA-005)copy SMILEScopy InChI
Affinity DataEC50:  130nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458133(US10752616, Code No. BHBA-005)copy SMILEScopy InChI
Affinity DataEC50:  55nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526313(CHEMBL4469143 | US10752616, Code No. BHBA-006)copy SMILEScopy InChI
Affinity DataEC50:  14nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526313(CHEMBL4469143 | US10752616, Code No. BHBA-006)copy SMILEScopy InChI
Affinity DataEC50:  89nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526313(CHEMBL4469143 | US10752616, Code No. BHBA-006)copy SMILEScopy InChI
Affinity DataEC50:  25nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526312(CHEMBL4449668 | US10752616, Code No. BHBA-007)copy SMILEScopy InChI
Affinity DataEC50:  2.20nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526312(CHEMBL4449668 | US10752616, Code No. BHBA-007)copy SMILEScopy InChI
Affinity DataEC50:  16nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM50526312(CHEMBL4449668 | US10752616, Code No. BHBA-007)copy SMILEScopy InChI
Affinity DataEC50:  8.40nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458145(US10752616, Code No. BHBA-008)copy SMILEScopy InChI
Affinity DataEC50:  1.90nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458145(US10752616, Code No. BHBA-008)copy SMILEScopy InChI
Affinity DataEC50:  17nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458145(US10752616, Code No. BHBA-008)copy SMILEScopy InChI
Affinity DataEC50:  6.80nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458150(US10752616, Code No. BHBA-009)copy SMILEScopy InChI
Affinity DataEC50:  4.20nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458150(US10752616, Code No. BHBA-009)copy SMILEScopy InChI
Affinity DataEC50:  32nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458150(US10752616, Code No. BHBA-009)copy SMILEScopy InChI
Affinity DataEC50:  11nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458152(US10752616, Code No. BHBA-010)copy SMILEScopy InChI
Affinity DataEC50:  2.90nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458152(US10752616, Code No. BHBA-010)copy SMILEScopy InChI
Affinity DataEC50:  25nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458152(US10752616, Code No. BHBA-010)copy SMILEScopy InChI
Affinity DataEC50:  0.530nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458158(US10752616, Code No. BHBA-011)copy SMILEScopy InChI
Affinity DataEC50:  4.30nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458158(US10752616, Code No. BHBA-011)copy SMILEScopy InChI
Affinity DataEC50:  26nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458158(US10752616, Code No. BHBA-011)copy SMILEScopy InChI
Affinity DataEC50:  14nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458165(US10752616, Code No. BHBA-012)copy SMILEScopy InChI
Affinity DataEC50:  17nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458165(US10752616, Code No. BHBA-012)copy SMILEScopy InChI
Affinity DataEC50:  67nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458165(US10752616, Code No. BHBA-012)copy SMILEScopy InChI
Affinity DataEC50:  17nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458201(US10752616, Code No. BHBA-013)copy SMILEScopy InChI
Affinity DataEC50:  16nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458201(US10752616, Code No. BHBA-013)copy SMILEScopy InChI
Affinity DataEC50:  140nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458201(US10752616, Code No. BHBA-013)copy SMILEScopy InChI
Affinity DataEC50:  110nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458233(US10752616, Code No. BHBA-014)copy SMILEScopy InChI
Affinity DataEC50:  2nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458233(US10752616, Code No. BHBA-014)copy SMILEScopy InChI
Affinity DataEC50:  12nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458233(US10752616, Code No. BHBA-014)copy SMILEScopy InChI
Affinity DataEC50:  11nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458240(US10752616, Code No. BHBA-015)copy SMILEScopy InChI
Affinity DataEC50:  2.90nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458240(US10752616, Code No. BHBA-015)copy SMILEScopy InChI
Affinity DataEC50:  23nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458240(US10752616, Code No. BHBA-015)copy SMILEScopy InChI
Affinity DataEC50:  12nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458251(US10752616, Code No. BHBA-016)copy SMILEScopy InChI
Affinity DataEC50:  2.70nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458251(US10752616, Code No. BHBA-016)copy SMILEScopy InChI
Affinity DataEC50:  18nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458251(US10752616, Code No. BHBA-016)copy SMILEScopy InChI
Affinity DataEC50:  6nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
TargetRetinoic acid receptor beta(Homo sapiens (Human))
King''s College London

US Patent
LigandPNGBDBM458259(US10752616, Code No. BHBA-017)copy SMILEScopy InChI
Affinity DataEC50:  7.40nMAssay Description:Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B85C6MUS Patent
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