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Compile Data Set for Download or QSAR

Found 258 hits of ic50 for UniProtKB: P03372   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521421
PNG
(6-(2,4- dichlorophenyl)- 1-fluoro-5-[6- [(3S)-1-(3...)
Show SMILES Oc1ccc2c(CCCC(c3ccc(Cl)cc3Cl)=C2c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c1F |r,c:18|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.400n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521255
PNG
(3-(6-ethoxy-2- fluoro-3- pyridyl)-4-[6- [(3S)-1-(3...)
Show SMILES CCOc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)nc3)c3ccc(O)cc3SC2)c(F)n1 |r,c:7|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.5n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521262
PNG
(6-(6-ethoxy-2- fluoro-3- pyridyl)-5-[4- [[(3S)-1-(...)
Show SMILES CCOc1ccc(c(F)n1)C1=C(c2ccc(N[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2CCC1 |r,c:11|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.5n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521384
PNG
(4-(6-ethoxy-2- fluoro-3- pyridyl)-5-[6- [(3S)-1-(3...)
Show SMILES CCOc1ccc(c(F)n1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2SCC1 |r,c:11|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.600n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521413
PNG
(6-(2-fluoro-4- methyl-phenyl)- 5-[6-[(3S)-1-(3- fl...)
Show SMILES Cc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2CCC1 |r,c:9|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.600n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521382
PNG
(4-(2-chloro-4- methyl-phenyl)- 5-[6-[(3S)-1-(3- fl...)
Show SMILES Cc1ccc(c(Cl)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2SCC1 |r,c:9|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.700n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521428
PNG
(6-(6-ethoxy-2- fluoro-3- pyridyl)-1- fluoro-5-[6- ...)
Show SMILES CCOc1ccc(c(F)n1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)c(F)c2CCC1 |r,c:11|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 0.700n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521360
PNG
(4-(benzofuran- 5-yl)-5-[4-[(3S)- 1-(3- fluoropropy...)
Show SMILES Oc1ccc2c(SCCC(c3ccc4occc4c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:20|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521261
PNG
(6-(2,4- dichlorophenyl)- 5-[4-[[(3S)-1- (3- fluoro...)
Show SMILES Oc1ccc2c(CCCC(c3ccc(Cl)cc3Cl)=C2c2ccc(N[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:18|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521362
PNG
(4-(4-ethoxy-2- methyl-phenyl)- 5-[4-[(3S)-1-(3- fl...)
Show SMILES CCOc1ccc(c(C)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:11|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521369
PNG
(4-(2,2-difluoro- 1,3- benzodioxol-5- yl)-5-[4-[(3S...)
Show SMILES Oc1ccc2c(SCCC(c3ccc4OC(F)(F)Oc4c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:22|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521373
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES CC1Cc2cc(ccc2O1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:12|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521374
PNG
(4-(2,2- dimethylindolin- 5-yl)-5-[4-[(3S)- 1-(3- f...)
Show SMILES CC1(C)Cc2cc(ccc2S1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:13|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521377
PNG
(4-(2,2-dimethyl- 3H-benzofuran- 5-yl)-5-[4-[(3S)- ...)
Show SMILES CC1(C)Cc2cc(ccc2O1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:13|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521378
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES C[C@@H]1Cc2cc(ccc2O1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:12|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521381
PNG
(4-(2,4- dichlorophenyl)- 5-[(6-[(3S)-1-(3- fluorop...)
Show SMILES Oc1ccc2c(SCCC(c3ccc(Cl)cc3Cl)=C2c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c1 |r,c:18|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521394
PNG
(4-[4- (fluoromethoxy) phenyl]-5-[4- [(3S)-1-(3- fl...)
Show SMILES Oc1ccc2c(SCCC(c3ccc(OCF)cc3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:19|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521417
PNG
(6-[4- (difluoromethoxy)- 3-fluoro- phenyl]-5-[6- [...)
Show SMILES Oc1ccc2c(CCCC(c3ccc(OC(F)F)c(F)c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c1 |r,c:21|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521418
PNG
(6-(2,2- dimethylindolin- 5-yl)-5-[6-[(3S)- 1-(3- f...)
Show SMILES CC1(C)Cc2cc(ccc2N1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2CCC1 |r,c:13|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521425
PNG
(6-[4- (difluoromethoxy)- 3-fluoro- phenyl]-1- fluo...)
Show SMILES Oc1ccc2c(CCCC(c3ccc(OC(F)F)c(F)c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c1F |r,c:21|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521334
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES Oc1cccc(c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:8|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521221
PNG
(3-(2-fluoro-6- methoxy-3- pyridyl)-4-[4- [(3S)-1-(...)
Show SMILES COc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)cc3)c3ccc(O)cc3SC2)c(F)n1 |r,c:6|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521254
PNG
(3-(2-fluoro-4- methyl-phenyl)- 4-[6-[(3S)-1-(3- fl...)
Show SMILES Cc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)nc3)c3ccc(O)cc3SC2)c(F)c1 |r,c:5|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521363
PNG
(4-(6-ethoxy-2- fluoro-3- pyridyl)-5-[4- [(3S)-1-(3...)
Show SMILES CCOc1ccc(c(F)n1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:11|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 1.5n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521297
PNG
(4-(2-fluoro-4- methoxy- phenyl)-5-[4- [(3S)-1-(3- ...)
Show SMILES COc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:10|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521270
PNG
(4-(2-fluoro-4- hydroxy- phenyl)-5-[4- [(3S)-1-(3- ...)
Show SMILES Oc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:9|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521383
PNG
(4-[4- (difluoromethoxy)- 3-fluoro- phenyl]-5-[6- [...)
Show SMILES Oc1ccc2c(SCCC(c3ccc(OC(F)F)c(F)c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)nc2)c1 |r,c:21|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521385
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES COc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:10|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521399
PNG
(4-(6-amino-2- fluoro-3- pyridyl)-5-[4- [(3S)-1-(3-...)
Show SMILES Nc1ccc(c(F)n1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:9|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 2n/an/an/an/an/an/a


TBA

Assay Description
Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521422
PNG
(6-(4-ethoxy- 2,3-difluoro- phenyl)-5-[2- [(3S)-1-(...)
Show SMILES CCOc1ccc(c(F)c1F)C1=C(c2cnc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2CCC1 |r,c:12|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521295
PNG
(4-(4-ethoxy-2- methyl-phenyl)- 5-[4-[(3S)-1-(3- fl...)
Show SMILES CCOc1ccc(c(C)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:11|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521296
PNG
(4-(benzofuran- 5-yl)-5-[4-[(3S)- 1-(3- fluoropropy...)
Show SMILES Oc1ccc2c(OCCC(c3ccc4occc4c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:20|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521297
PNG
(4-(2-fluoro-4- methoxy- phenyl)-5-[4- [(3S)-1-(3- ...)
Show SMILES COc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:10|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521333
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES COc1ccc(c(C)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:10|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521345
PNG
(4-(2-fluoro-4- hydroxy- phenyl)-5-[4- [(3S)-1-(3- ...)
Show SMILES Oc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:9|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521354
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES Oc1ccc2c(SCCC(c3cccc4[nH]ccc34)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:20|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521182
PNG
(7-(2-fluoro-4- hydroxy- phenyl)-8-[4- [(3S)-1-(3- ...)
Show SMILES Oc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)cc3)c3cc(O)ccc3CC2)c(F)c1 |r,c:5|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521203
PNG
(3-(6-ethoxy-2- fluoro-3- pyridyl)-4-[4- [(3S)-1-(3...)
Show SMILES CCOc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)cc3)c3ccc(O)cc3SC2)c(F)n1 |r,c:7|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521229
PNG
(3-(3-chloro-2- ethoxy-4- pyridyl)-4-[4- [(3S)-1-(3...)
Show SMILES CCOc1nccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)cc3)c3ccc(O)cc3SC2)c1Cl |r,c:8|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521267
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES Oc1cccc(c1)C1=C(c2ccc(N[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:8|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521361
PNG
(4-(4-ethoxy-3- fluoro-phenyl)- 5-[4-[(3S)-1-(3- fl...)
Show SMILES CCOc1ccc(cc1F)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:11|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521367
PNG
(4-[4- (difluoromethoxy)- 3-fluoro- phenyl]-5-[4- [...)
Show SMILES Oc1ccc2c(SCCC(c3ccc(OC(F)F)c(F)c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:21|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521372
PNG
(4-(4-ethoxy-2- fluoro-phenyl)- 5-[4-[(3S)-1-(3- fl...)
Show SMILES CCOc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:11|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521376
PNG
(4-[4- (ethylamino)-2- fluoro-phenyl]- 5-[4-[(3S)-...)
Show SMILES CCNc1ccc(c(F)c1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2SCC1 |r,c:11|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521414
PNG
(6-(2,4- dichlorophenyl)- 5-[2-[(3S)-1-(3- fluoropr...)
Show SMILES Oc1ccc2c(CCCC(c3ccc(Cl)cc3Cl)=C2c2cnc(O[C@H]3CCN(CCCF)C3)nc2)c1 |r,c:18|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521420
PNG
(6-(2-fluoro-4- methyl-phenyl)- 5-[2-[(3S)-1-(3- fl...)
Show SMILES Cc1ccc(c(F)c1)C1=C(c2cnc(O[C@H]3CCN(CCCF)C3)nc2)c2ccc(O)cc2CCC1 |r,c:9|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521298
PNG
(4-(2,3- dimethylphenyl)- 5-[4-[(3S)-1-(3- fluoropr...)
Show SMILES Cc1cccc(c1C)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(O)cc2OCC1 |r,c:9|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521202
PNG
(3-(4-ethoxy-2- fluoro-phenyl)- 4-[4-[(3S)-1-(3- fl...)
Show SMILES CCOc1ccc(C2=C(c3ccc(O[C@H]4CCN(CCCF)C4)cc3)c3ccc(O)cc3SC2)c(F)c1 |r,c:7|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521335
PNG
(4-(2-chloro-4- fluoro-phenyl)- 5-[4-[(3S)-1-(3- fl...)
Show SMILES Oc1ccc2c(SCCC(c3ccc(F)cc3Cl)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:18|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
Estrogen receptor [298-554]


(Homo sapiens (Human))
BDBM521336
PNG
(5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]o...)
Show SMILES Oc1ccc2c(SCCC(c3ccc4[nH]ccc4c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:20|
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Antagonistic potency of compounds was evaluated using LanthaScreenŽ TR-FRET ERα Coactivator Assay (ThermoFisher) with modifications. It is a com...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2NZ8BT3
More data for this
Ligand-Target Pair
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