Compile Data Set for Download or QSAR
Report error Found 136 Enz. Inhib. hit(s) with all data for entry = 9322
TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458152BDBM458152(US10752616, Code No. BHBA-010)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 323588BDBM323588(Retinoic Acid | all-trans-retinoic acid | at-RA | ...)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor alpha(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 323588BDBM323588(Retinoic Acid | all-trans-retinoic acid | at-RA | ...)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 323588BDBM323588(Retinoic Acid | all-trans-retinoic acid | at-RA | ...)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458145BDBM458145(US10752616, Code No. BHBA-008)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526314BDBM50526314(CHEMBL4459692 | US10752616, Code No. BHBA-001)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458233BDBM458233(US10752616, Code No. BHBA-014)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458286BDBM458286(US10752616, Code No. BHBA-044)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526312BDBM50526312(CHEMBL4449668 | US10752616, Code No. BHBA-007)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458284BDBM458284(US10752616, Code No. BHBA-042)
Affinity DataEC50:  2.30nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526315BDBM50526315(CHEMBL4439399 | US10752616, Code No. BHBA-019)
Affinity DataEC50:  2.5nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458251BDBM458251(US10752616, Code No. BHBA-016)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458152BDBM458152(US10752616, Code No. BHBA-010)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458240BDBM458240(US10752616, Code No. BHBA-015)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458284BDBM458284(US10752616, Code No. BHBA-042)
Affinity DataEC50:  3.10nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526325BDBM50526325(CHEMBL4438880 | US10752616, Code No. BHBA-021)
Affinity DataEC50:  3.40nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458286BDBM458286(US10752616, Code No. BHBA-044)
Affinity DataEC50:  3.40nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458281BDBM458281(US10752616, Code No. BHBA-039)
Affinity DataEC50:  3.60nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458287BDBM458287(US10752616, Code No. BHBA-045)
Affinity DataEC50:  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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458150BDBM458150(US10752616, Code No. BHBA-009)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458283BDBM458283(US10752616, Code No. BHBA-041)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458158BDBM458158(US10752616, Code No. BHBA-011)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458283BDBM458283(US10752616, Code No. BHBA-041)
Affinity DataEC50:  4.70nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458280BDBM458280(US10752616, Code No. BHBA-038)
Affinity DataEC50:  5.10nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458285BDBM458285(US10752616, Code No. BHBA-043)
Affinity DataEC50:  5.20nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526315BDBM50526315(CHEMBL4439399 | US10752616, Code No. BHBA-019)
Affinity DataEC50:  5.30nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458251BDBM458251(US10752616, Code No. BHBA-016)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458280BDBM458280(US10752616, Code No. BHBA-038)
Affinity DataEC50:  6.10nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526325BDBM50526325(CHEMBL4438880 | US10752616, Code No. BHBA-021)
Affinity DataEC50:  6.30nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458145BDBM458145(US10752616, Code No. BHBA-008)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458259BDBM458259(US10752616, Code No. BHBA-017)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458262BDBM458262(US10752616, Code No. BHBA-020)
Affinity DataEC50:  8nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458274BDBM458274(US10752616, Code No. BHBA-032)
Affinity DataEC50:  8.10nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458270BDBM458270(US10752616, Code No. BHBA-028)
Affinity DataEC50:  8.20nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458270BDBM458270(US10752616, Code No. BHBA-028)
Affinity DataEC50:  8.30nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526312BDBM50526312(CHEMBL4449668 | US10752616, Code No. BHBA-007)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458269BDBM458269(US10752616, Code No. BHBA-027)
Affinity DataEC50:  9nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor alpha(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458284BDBM458284(US10752616, Code No. BHBA-042)
Affinity DataEC50:  9.40nMAssay 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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458127BDBM458127(US10752616, Code No. BHBA-004)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458272BDBM458272(US10752616, Code No. BHBA-030)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458233BDBM458233(US10752616, Code No. BHBA-014)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458150BDBM458150(US10752616, Code No. BHBA-009)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458282BDBM458282(US10752616, Code No. BHBA-040)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526314BDBM50526314(CHEMBL4459692 | US10752616, Code No. BHBA-001)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 50526327BDBM50526327(CHEMBL4562084 | US10752616, Code No. BHBA-023)
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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458121BDBM458121(US10752616, Code No. BHBA-002)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458240BDBM458240(US10752616, Code No. BHBA-015)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor alpha(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458233BDBM458233(US10752616, Code No. BHBA-014)
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
In Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor beta(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458268BDBM458268(US10752616, Code No. BHBA-026)
Affinity DataEC50:  13nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

TargetRetinoic acid receptor gamma(Human)
King''S College London

US Patent
LigandChemical structure of BindingDB Monomer ID 458281BDBM458281(US10752616, Code No. BHBA-039)
Affinity DataEC50:  13nMAssay 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 Depth
Date in BDB:
4/11/2021
Entry Details
US Patent

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