Compile Data Set for Download or QSAR
Report error Found 20 Enz. Inhib. hit(s) with all data for entry = 5965
TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102984BDBM102984(US8546451, II)
Affinity DataKi:  3.75nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102985BDBM102985(US8546451, III)
Affinity DataKi:  3.81nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102989BDBM102989(US8546451, VII)
Affinity DataKi:  6.06nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102985BDBM102985(US8546451, III)
Affinity DataKi:  6.44nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102987BDBM102987(US8546451, V)
Affinity DataKi:  7.13nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102988BDBM102988(US8546451, VI)
Affinity DataKi:  9nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102990BDBM102990(US8546451, VIII)
Affinity DataKi:  13nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102991BDBM102991(US8546451, IX (or X))
Affinity DataKi:  14.8nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102992BDBM102992(US8546451, XI)
Affinity DataKi:  15nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102993BDBM102993(US8546451, XII)
Affinity DataKi:  15.1nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102986BDBM102986(US8546451, IV)
Affinity DataKi:  15.2nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102990BDBM102990(US8546451, VIII)
Affinity DataKi:  19nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102986BDBM102986(US8546451, IV)
Affinity DataKi:  21.7nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102993BDBM102993(US8546451, XII)
Affinity DataKi:  25.0nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102987BDBM102987(US8546451, V)
Affinity DataKi:  35.9nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102992BDBM102992(US8546451, XI)
Affinity DataKi:  57nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102988BDBM102988(US8546451, VI)
Affinity DataKi:  72nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102989BDBM102989(US8546451, VII)
Affinity DataKi:  76.9nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102984BDBM102984(US8546451, II)
Affinity DataKi:  81.6nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent

TargetEstrogen receptor beta(Human)
Gtx

US Patent
LigandChemical structure of BindingDB Monomer ID 102991BDBM102991(US8546451, IX (or X))
Affinity DataKi:  646nMAssay Description:The ER binding affinity of the compounds was determined using an in vitro competitive radioligand binding assay was [2,4,6,7-3H(N)]-Estradiol ([3H]E2...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2013
Entry Details
US Patent