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Compile Data Set for Download or QSAR

Found 43 hits with Last Name = 'lasek' and Initial = 'aw'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Estrogen receptor


(Homo sapiens (Human))
BDBM50514279
PNG
(CHEMBL4527655)
Show SMILES CC1CN(CCOc2ccc(Oc3c(sc4cc(O)ccc34)C(=O)c3ccccc3C)cc2)C1
Show InChI InChI=1S/C28H27NO4S/c1-18-16-29(17-18)13-14-32-21-8-10-22(11-9-21)33-27-24-12-7-20(30)15-25(24)34-28(27)26(31)23-6-4-3-5-19(23)2/h3-12,15,18,30H,13-14,16-17H2,1-2H3
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n/an/a 0.257n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514280
PNG
(CHEMBL4586663)
Show SMILES Oc1ccc2c(Oc3ccc(OC4CN(CCCF)C4)cc3)c(sc2c1)C(=O)c1ccccc1
Show InChI InChI=1S/C27H24FNO4S/c28-13-4-14-29-16-22(17-29)32-20-8-10-21(11-9-20)33-26-23-12-7-19(30)15-24(23)34-27(26)25(31)18-5-2-1-3-6-18/h1-3,5-12,15,22,30H,4,13-14,16-17H2
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n/an/a 0.5n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514280
PNG
(CHEMBL4586663)
Show SMILES Oc1ccc2c(Oc3ccc(OC4CN(CCCF)C4)cc3)c(sc2c1)C(=O)c1ccccc1
Show InChI InChI=1S/C27H24FNO4S/c28-13-4-14-29-16-22(17-29)32-20-8-10-21(11-9-20)33-26-23-12-7-19(30)15-24(23)34-27(26)25(31)18-5-2-1-3-6-18/h1-3,5-12,15,22,30H,4,13-14,16-17H2
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n/an/a 0.708n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514287
PNG
(CHEMBL4532671)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H26FNO4S/c1-18-4-2-3-5-23(18)26(32)28-27(24-11-6-20(31)14-25(24)35-28)34-22-9-7-21(8-10-22)33-13-12-30-16-19(15-29)17-30/h2-11,14,19,31H,12-13,15-17H2,1H3
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n/an/a 0.955n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514293
PNG
(CHEMBL4515212)
Show SMILES Oc1ccc2c(Oc3ccc(OCCN4CC(CF)C4)cc3)c(sc2c1)C(=O)c1ccccc1
Show InChI InChI=1S/C27H24FNO4S/c28-15-18-16-29(17-18)12-13-32-21-7-9-22(10-8-21)33-26-23-11-6-20(30)14-24(23)34-27(26)25(31)19-4-2-1-3-5-19/h1-11,14,18,30H,12-13,15-17H2
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n/an/a 1n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514292
PNG
(CHEMBL4533964)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C29H27F2NO4S/c1-17-12-19(31)13-18(2)26(17)27(34)29-28(24-9-4-20(33)14-25(24)37-29)36-22-7-5-21(6-8-22)35-23-15-32(16-23)11-3-10-30/h4-9,12-14,23,33H,3,10-11,15-16H2,1-2H3
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n/an/a 1n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514283
PNG
(CHEMBL4524872)
Show SMILES Oc1ccc2c(Oc3ccc(OCCN4CC(CF)C4)cc3)c(sc2c1)C(=O)c1ccc(F)cc1
Show InChI InChI=1S/C27H23F2NO4S/c28-14-17-15-30(16-17)11-12-33-21-6-8-22(9-7-21)34-26-23-10-5-20(31)13-24(23)35-27(26)25(32)18-1-3-19(29)4-2-18/h1-10,13,17,31H,11-12,14-16H2
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n/an/a 1.20n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514282
PNG
(CHEMBL4543096)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C29H27F2NO4S/c1-17-11-20(31)12-18(2)26(17)27(34)29-28(24-8-3-21(33)13-25(24)37-29)36-23-6-4-22(5-7-23)35-10-9-32-15-19(14-30)16-32/h3-8,11-13,19,33H,9-10,14-16H2,1-2H3
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n/an/a 1.40n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514284
PNG
(CHEMBL4483006)
Show SMILES Cc1ccc(C(=O)c2sc3cc(O)ccc3c2Oc2ccc(OCCN3CC(CF)C3)cc2)c(C)c1
Show InChI InChI=1S/C29H28FNO4S/c1-18-3-9-24(19(2)13-18)27(33)29-28(25-10-4-21(32)14-26(25)36-29)35-23-7-5-22(6-8-23)34-12-11-31-16-20(15-30)17-31/h3-10,13-14,20,32H,11-12,15-17H2,1-2H3
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n/an/a 1.40n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514287
PNG
(CHEMBL4532671)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H26FNO4S/c1-18-4-2-3-5-23(18)26(32)28-27(24-11-6-20(31)14-25(24)35-28)34-22-9-7-21(8-10-22)33-13-12-30-16-19(15-29)17-30/h2-11,14,19,31H,12-13,15-17H2,1H3
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n/an/a 1.5n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50238741
PNG
(CHEBI:31638 | Faslodex | Fulvestrant | ICI-182780 ...)
Show SMILES [H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])c3ccc(O)cc3C[C@@H](CCCCCCCCC[S+]([O-])CCCC(F)(F)C(F)(F)F)[C@@]21[H]
Show InChI InChI=1S/C32H47F5O3S/c1-30-17-15-26-25-12-11-24(38)21-23(25)20-22(29(26)27(30)13-14-28(30)39)10-7-5-3-2-4-6-8-18-41(40)19-9-16-31(33,34)32(35,36)37/h11-12,21-22,26-29,38-39H,2-10,13-20H2,1H3/t22-,26-,27+,28+,29-,30+,41?/m1/s1
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n/an/a 1.60n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514281
PNG
(CHEMBL4516021)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CCC2)cc1
Show InChI InChI=1S/C27H25NO4S/c1-18-5-2-3-6-22(18)25(30)27-26(23-12-7-19(29)17-24(23)33-27)32-21-10-8-20(9-11-21)31-16-15-28-13-4-14-28/h2-3,5-12,17,29H,4,13-16H2,1H3
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n/an/a 1.90n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514279
PNG
(CHEMBL4527655)
Show SMILES CC1CN(CCOc2ccc(Oc3c(sc4cc(O)ccc34)C(=O)c3ccccc3C)cc2)C1
Show InChI InChI=1S/C28H27NO4S/c1-18-16-29(17-18)13-14-32-21-8-10-22(11-9-21)33-27-24-12-7-20(30)15-25(24)34-28(27)26(31)23-6-4-3-5-19(23)2/h3-12,15,18,30H,13-14,16-17H2,1-2H3
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n/an/a 1.90n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514286
PNG
(CHEMBL4448178)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C28H26FNO4S/c1-18-5-2-3-6-23(18)26(32)28-27(24-12-7-19(31)15-25(24)35-28)34-21-10-8-20(9-11-21)33-22-16-30(17-22)14-4-13-29/h2-3,5-12,15,22,31H,4,13-14,16-17H2,1H3
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n/an/a 2.10n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514286
PNG
(CHEMBL4448178)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C28H26FNO4S/c1-18-5-2-3-6-23(18)26(32)28-27(24-12-7-19(31)15-25(24)35-28)34-21-10-8-20(9-11-21)33-22-16-30(17-22)14-4-13-29/h2-3,5-12,15,22,31H,4,13-14,16-17H2,1H3
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n/an/a 2.60n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514290
PNG
(CHEMBL4578883)
Show SMILES Cc1cc(F)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H25F2NO4S/c1-17-12-19(30)2-8-23(17)26(33)28-27(24-9-3-20(32)13-25(24)36-28)35-22-6-4-21(5-7-22)34-11-10-31-15-18(14-29)16-31/h2-9,12-13,18,32H,10-11,14-16H2,1H3
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n/an/a 2.70n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514285
PNG
(CHEMBL4436707)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC[C@H](CF)C2)cc1 |r|
Show InChI InChI=1S/C30H29F2NO4S/c1-18-13-21(32)14-19(2)27(18)28(35)30-29(25-8-3-22(34)15-26(25)38-30)37-24-6-4-23(5-7-24)36-12-11-33-10-9-20(16-31)17-33/h3-8,13-15,20,34H,9-12,16-17H2,1-2H3/t20-/m1/s1
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n/an/a 3n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514292
PNG
(CHEMBL4533964)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C29H27F2NO4S/c1-17-12-19(31)13-18(2)26(17)27(34)29-28(24-9-4-20(33)14-25(24)37-29)36-22-7-5-21(6-8-22)35-23-15-32(16-23)11-3-10-30/h4-9,12-14,23,33H,3,10-11,15-16H2,1-2H3
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n/an/a 3.10n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514282
PNG
(CHEMBL4543096)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C29H27F2NO4S/c1-17-11-20(31)12-18(2)26(17)27(34)29-28(24-8-3-21(33)13-25(24)37-29)36-23-6-4-22(5-7-23)35-10-9-32-15-19(14-30)16-32/h3-8,11-13,19,33H,9-10,14-16H2,1-2H3
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n/an/a 3.5n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514290
PNG
(CHEMBL4578883)
Show SMILES Cc1cc(F)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H25F2NO4S/c1-17-12-19(30)2-8-23(17)26(33)28-27(24-9-3-20(32)13-25(24)36-28)35-22-6-4-21(5-7-22)34-11-10-31-15-18(14-29)16-31/h2-9,12-13,18,32H,10-11,14-16H2,1H3
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n/an/a 3.60n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514293
PNG
(CHEMBL4515212)
Show SMILES Oc1ccc2c(Oc3ccc(OCCN4CC(CF)C4)cc3)c(sc2c1)C(=O)c1ccccc1
Show InChI InChI=1S/C27H24FNO4S/c28-15-18-16-29(17-18)12-13-32-21-7-9-22(10-8-21)33-26-23-11-6-20(30)14-24(23)34-27(26)25(31)19-4-2-1-3-5-19/h1-11,14,18,30H,12-13,15-17H2
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n/an/a 4.30n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514294
PNG
(CHEMBL4564385)
Show SMILES Cc1cc(O)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H26FNO5S/c1-17-12-19(31)2-8-23(17)26(33)28-27(24-9-3-20(32)13-25(24)36-28)35-22-6-4-21(5-7-22)34-11-10-30-15-18(14-29)16-30/h2-9,12-13,18,31-32H,10-11,14-16H2,1H3
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n/an/a 5.10n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514289
PNG
(CHEMBL4538085)
Show SMILES Cc1cc(F)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C28H25F2NO4S/c1-17-13-18(30)3-9-23(17)26(33)28-27(24-10-4-19(32)14-25(24)36-28)35-21-7-5-20(6-8-21)34-22-15-31(16-22)12-2-11-29/h3-10,13-14,22,32H,2,11-12,15-16H2,1H3
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n/an/a 5.20n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514295
PNG
(CHEMBL4440649)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC[C@@H](CF)C2)cc1 |r|
Show InChI InChI=1S/C30H29F2NO4S/c1-18-13-21(32)14-19(2)27(18)28(35)30-29(25-8-3-22(34)15-26(25)38-30)37-24-6-4-23(5-7-24)36-12-11-33-10-9-20(16-31)17-33/h3-8,13-15,20,34H,9-12,16-17H2,1-2H3/t20-/m0/s1
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n/an/a 5.90n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514278
PNG
(CHEMBL4436415)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(C2)C2CC2)cc1
Show InChI InChI=1S/C29H26FNO4S/c1-16-11-18(30)12-17(2)26(16)27(33)29-28(24-10-5-20(32)13-25(24)36-29)35-22-8-6-21(7-9-22)34-23-14-31(15-23)19-3-4-19/h5-13,19,23,32H,3-4,14-15H2,1-2H3
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n/an/a 5.90n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514284
PNG
(CHEMBL4483006)
Show SMILES Cc1ccc(C(=O)c2sc3cc(O)ccc3c2Oc2ccc(OCCN3CC(CF)C3)cc2)c(C)c1
Show InChI InChI=1S/C29H28FNO4S/c1-18-3-9-24(19(2)13-18)27(33)29-28(25-10-4-21(32)14-26(25)36-29)35-23-7-5-22(6-8-23)34-12-11-31-16-20(15-30)17-31/h3-10,13-14,20,32H,11-12,15-17H2,1-2H3
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n/an/a 7.40n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514288
PNG
(CHEMBL4464171)
Show SMILES Oc1ccc(cc1)C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C27H24FNO5S/c28-14-17-15-29(16-17)11-12-33-21-6-8-22(9-7-21)34-26-23-10-5-20(31)13-24(23)35-27(26)25(32)18-1-3-19(30)4-2-18/h1-10,13,17,30-31H,11-12,14-16H2
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n/an/a 8.10n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514289
PNG
(CHEMBL4538085)
Show SMILES Cc1cc(F)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(CCCF)C2)cc1
Show InChI InChI=1S/C28H25F2NO4S/c1-17-13-18(30)3-9-23(17)26(33)28-27(24-10-4-19(32)14-25(24)36-28)35-21-7-5-20(6-8-21)34-22-15-31(16-22)12-2-11-29/h3-10,13-14,22,32H,2,11-12,15-16H2,1H3
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n/an/a 9.30n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514291
PNG
(CHEMBL4447374)
Show SMILES Cc1ccccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC[C@@H](CF)C2)cc1 |r|
Show InChI InChI=1S/C29H28FNO4S/c1-19-4-2-3-5-24(19)27(33)29-28(25-11-6-21(32)16-26(25)36-29)35-23-9-7-22(8-10-23)34-15-14-31-13-12-20(17-30)18-31/h2-11,16,20,32H,12-15,17-18H2,1H3/t20-/m0/s1
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n/an/a 10n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Inhibition of ERalpha in human MCF7:WS8 cells assessed as increase in degradation of ERalpha incubated for 24 hrs by In-Cell Western assay


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514278
PNG
(CHEMBL4436415)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OC2CN(C2)C2CC2)cc1
Show InChI InChI=1S/C29H26FNO4S/c1-16-11-18(30)12-17(2)26(16)27(33)29-28(24-10-5-20(32)13-25(24)36-29)35-22-8-6-21(7-9-22)34-23-14-31(15-23)19-3-4-19/h5-13,19,23,32H,3-4,14-15H2,1-2H3
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n/an/a 11n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514295
PNG
(CHEMBL4440649)
Show SMILES Cc1cc(F)cc(C)c1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC[C@@H](CF)C2)cc1 |r|
Show InChI InChI=1S/C30H29F2NO4S/c1-18-13-21(32)14-19(2)27(18)28(35)30-29(25-8-3-22(34)15-26(25)38-30)37-24-6-4-23(5-7-24)36-12-11-33-10-9-20(16-31)17-33/h3-8,13-15,20,34H,9-12,16-17H2,1-2H3/t20-/m0/s1
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n/an/a 12n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514294
PNG
(CHEMBL4564385)
Show SMILES Cc1cc(O)ccc1C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C28H26FNO5S/c1-17-12-19(31)2-8-23(17)26(33)28-27(24-9-3-20(32)13-25(24)36-28)35-22-6-4-21(5-7-22)34-11-10-30-15-18(14-29)16-30/h2-9,12-13,18,31-32H,10-11,14-16H2,1H3
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n/an/a 14n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514283
PNG
(CHEMBL4524872)
Show SMILES Oc1ccc2c(Oc3ccc(OCCN4CC(CF)C4)cc3)c(sc2c1)C(=O)c1ccc(F)cc1
Show InChI InChI=1S/C27H23F2NO4S/c28-14-17-15-30(16-17)11-12-33-21-6-8-22(9-7-21)34-26-23-10-5-20(31)13-24(23)35-27(26)25(32)18-1-3-19(29)4-2-18/h1-10,13,17,31H,11-12,14-16H2
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n/an/a 28n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50514288
PNG
(CHEMBL4464171)
Show SMILES Oc1ccc(cc1)C(=O)c1sc2cc(O)ccc2c1Oc1ccc(OCCN2CC(CF)C2)cc1
Show InChI InChI=1S/C27H24FNO5S/c28-14-17-15-29(16-17)11-12-33-21-6-8-22(9-7-21)34-26-23-10-5-20(31)13-24(23)35-27(26)25(32)18-1-3-19(30)4-2-18/h1-10,13,17,30-31H,11-12,14-16H2
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n/an/a 64n/an/an/an/an/an/a



University of Illinois at Chicago

Curated by ChEMBL


Assay Description
Antagonist activity at ERalpha in human MCF7:WS8 cells incubated for 18 hrs by dual luciferase reporter gene assay relative to control


J Med Chem 62: 11301-11323 (2019)


Article DOI: 10.1021/acs.jmedchem.9b01580
BindingDB Entry DOI: 10.7270/Q2K64NDQ
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464775
PNG
(CHEMBL4278170)
Show SMILES FC(F)(F)Sc1ccc(CNCc2ccc(SC(F)(F)F)cc2)cc1
Show InChI InChI=1S/C16H13F6NS2/c17-15(18,19)24-13-5-1-11(2-6-13)9-23-10-12-3-7-14(8-4-12)25-16(20,21)22/h1-8,23H,9-10H2
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n/an/a 100n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464778
PNG
(CHEMBL4285054)
Show SMILES FC(F)(F)Sc1ccc(COc2ccc(SC(F)(F)F)cc2)cc1
Show InChI InChI=1S/C15H10F6OS2/c16-14(17,18)23-12-5-1-10(2-6-12)9-22-11-3-7-13(8-4-11)24-15(19,20)21/h1-8H,9H2
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n/an/a 100n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1


(Homo sapiens (Human))
BDBM50464775
PNG
(CHEMBL4278170)
Show SMILES FC(F)(F)Sc1ccc(CNCc2ccc(SC(F)(F)F)cc2)cc1
Show InChI InChI=1S/C16H13F6NS2/c17-15(18,19)24-13-5-1-11(2-6-13)9-23-10-12-3-7-14(8-4-12)25-16(20,21)22/h1-8,23H,9-10H2
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n/an/a 700n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTP1B using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464773
PNG
(CHEMBL4286807)
Show SMILES FC(F)(F)Sc1ccc(CNC(=O)Cc2ccc(SC(F)(F)F)cc2)cc1
Show InChI InChI=1S/C17H13F6NOS2/c18-16(19,20)26-13-5-1-11(2-6-13)9-15(25)24-10-12-3-7-14(8-4-12)27-17(21,22)23/h1-8H,9-10H2,(H,24,25)
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n/an/a 800n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1


(Homo sapiens (Human))
BDBM50464772
PNG
(CHEMBL4293314)
Show SMILES FC(F)(F)Sc1ccc(NCc2ccccc2)cc1
Show InChI InChI=1S/C14H12F3NS/c15-14(16,17)19-13-8-6-12(7-9-13)18-10-11-4-2-1-3-5-11/h1-9,18H,10H2
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n/an/a 1.00E+3n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTP1B using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464777
PNG
(CHEMBL4286401)
Show SMILES FC(F)(F)S(=O)(=O)c1ccc(COc2ccc(cc2)S(=O)(=O)C(F)(F)F)cc1
Show InChI InChI=1S/C15H10F6O5S2/c16-14(17,18)27(22,23)12-5-1-10(2-6-12)9-26-11-3-7-13(8-4-11)28(24,25)15(19,20)21/h1-8H,9H2
PDB

UniProtKB/SwissProt

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3.50E+3n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of PTPRZ1 (unknown origin) using pNPP as substrate preincubated for 15 mins followed by substrate addition measured after 10 mins by spect...


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464772
PNG
(CHEMBL4293314)
Show SMILES FC(F)(F)Sc1ccc(NCc2ccccc2)cc1
Show InChI InChI=1S/C14H12F3NS/c15-14(16,17)19-13-8-6-12(7-9-13)18-10-11-4-2-1-3-5-11/h1-9,18H,10H2
PDB

UniProtKB/SwissProt

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UniChem
Article
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n/an/a 5.00E+3n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464774
PNG
(CHEMBL4285322)
Show SMILES FC(F)(F)S(=O)(=O)c1ccc(CC(=O)Nc2ccc(cc2)S(=O)(=O)C(F)(F)F)cc1
Show InChI InChI=1S/C16H11F6NO5S2/c17-15(18,19)29(25,26)12-5-1-10(2-6-12)9-14(24)23-11-3-7-13(8-4-11)30(27,28)16(20,21)22/h1-8H,9H2,(H,23,24)
PDB

UniProtKB/SwissProt

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PC cid
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UniChem
Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase zeta


(Homo sapiens)
BDBM50464776
PNG
(CHEMBL4279566)
Show SMILES FC(F)(F)Sc1ccc(CNC(=O)c2ccc(SC(F)(F)F)cc2)cc1
Show InChI InChI=1S/C16H11F6NOS2/c17-15(18,19)25-12-5-1-10(2-6-12)9-23-14(24)11-3-7-13(8-4-11)26-16(20,21)22/h1-8H,9H2,(H,23,24)
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Universidad San Pablo-CEU

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PTPRZ1 using pNPP as substrate by fluorescence spectrometric analysis


Eur J Med Chem 144: 318-329 (2018)


Article DOI: 10.1016/j.ejmech.2017.11.080
BindingDB Entry DOI: 10.7270/Q2C53PHW
More data for this
Ligand-Target Pair