Found 50 hits with Last Name = 'redden' and Initial = 'pr' Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM20608
(4-Hydroxytamoxifen | 4-Hydroxytamoxifen (9) | 4-[(...)Show SMILES CC\C(=C(/c1ccc(O)cc1)c1ccc(OCCN(C)C)cc1)c1ccccc1 Show InChI InChI=1S/C26H29NO2/c1-4-25(20-8-6-5-7-9-20)26(21-10-14-23(28)15-11-21)22-12-16-24(17-13-22)29-19-18-27(2)3/h5-17,28H,4,18-19H2,1-3H3/b26-25- | PDB
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| PDB
Article
PubMed
| 0.160 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Estrogen receptor
(Homo sapiens (Human)) | BDBM20608
(4-Hydroxytamoxifen | 4-Hydroxytamoxifen (9) | 4-[(...)Show SMILES CC\C(=C(/c1ccc(O)cc1)c1ccc(OCCN(C)C)cc1)c1ccccc1 Show InChI InChI=1S/C26H29NO2/c1-4-25(20-8-6-5-7-9-20)26(21-10-14-23(28)15-11-21)22-12-16-24(17-13-22)29-19-18-27(2)3/h5-17,28H,4,18-19H2,1-3H3/b26-25- | PDB
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Article
PubMed
| 0.25 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Estrogen receptor
(Homo sapiens (Human)) | BDBM20625
(4-[(3E)-4-(4-hydroxyphenyl)hex-3-en-3-yl]phenol | ...)Show InChI InChI=1S/C18H20O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,19-20H,3-4H2,1-2H3/b18-17+ | PDB
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| 0.490 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM20625
(4-[(3E)-4-(4-hydroxyphenyl)hex-3-en-3-yl]phenol | ...)Show InChI InChI=1S/C18H20O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,19-20H,3-4H2,1-2H3/b18-17+ | PDB
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| 0.630 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50169743
((13S,17S)-13-Methyl-7-[9-(4,4,5,5,5-pentafluoro-pe...)Show SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)[C@H](CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F)Cc1cc(O)ccc31 |r| 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 | PDB
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| 1.04 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50169743
((13S,17S)-13-Methyl-7-[9-(4,4,5,5,5-pentafluoro-pe...)Show SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)[C@H](CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F)Cc1cc(O)ccc31 |r| 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 | PDB
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| 1.39 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126767
(7-Ethyl-4-methyl-9-[4-(2-piperidin-1-yl-ethoxy)-ph...)Show SMILES CCc1ccc-2c(c1)C(Cc1cc(O)cc(C)c-21)c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H35NO2/c1-3-22-7-12-27-29(18-22)28(20-24-19-25(32)17-21(2)30(24)27)23-8-10-26(11-9-23)33-16-15-31-13-5-4-6-14-31/h7-12,17-19,28,32H,3-6,13-16,20H2,1-2H3 | PDB
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PC sid
UniChem
| Article
PubMed
| 8.69 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126766
(7-(1-Hydroxy-ethyl)-4-methyl-9-[4-(2-piperidin-1-y...)Show SMILES CC(O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H33NO3/c1-20-16-25(33)17-24-19-28(29-18-23(21(2)32)8-11-27(29)30(20)24)22-6-9-26(10-7-22)34-15-14-31-12-4-3-5-13-31/h6-11,16-19,21,32-33H,3-5,12-15H2,1-2H3 | PDB
UniProtKB/SwissProt
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PC sid
UniChem
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| Article
PubMed
| 120 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126772
(7-Isopropenyl-4-methyl-9-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(=C)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C31H33NO2/c1-21(2)24-9-12-28-30(19-24)29(20-25-18-26(33)17-22(3)31(25)28)23-7-10-27(11-8-23)34-16-15-32-13-5-4-6-14-32/h7-12,17-20,33H,1,4-6,13-16H2,2-3H3 | PDB
UniProtKB/SwissProt
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| CHEMBL
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PC sid
UniChem
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| Article
PubMed
| 180 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126767
(7-Ethyl-4-methyl-9-[4-(2-piperidin-1-yl-ethoxy)-ph...)Show SMILES CCc1ccc-2c(c1)C(Cc1cc(O)cc(C)c-21)c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H35NO2/c1-3-22-7-12-27-29(18-22)28(20-24-19-25(32)17-21(2)30(24)27)23-8-10-26(11-9-23)33-16-15-31-13-5-4-6-14-31/h7-12,17-19,28,32H,3-6,13-16,20H2,1-2H3 | PDB
UniProtKB/SwissProt
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| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| 190 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126766
(7-(1-Hydroxy-ethyl)-4-methyl-9-[4-(2-piperidin-1-y...)Show SMILES CC(O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H33NO3/c1-20-16-25(33)17-24-19-28(29-18-23(21(2)32)8-11-27(29)30(20)24)22-6-9-26(10-7-22)34-15-14-31-12-4-3-5-13-31/h6-11,16-19,21,32-33H,3-5,12-15H2,1-2H3 | PDB
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PubMed
| 190 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126770
(7-(1,2-Dimethyl-propenyl)-4-methyl-9-[4-(2-piperid...)Show SMILES [#6]\[#6](-[#6])=[#6](\[#6])-c1ccc2c(c1)c(cc1cc(-[#8])cc(-[#6])c21)-c1ccc(-[#8]-[#6]-[#6]-[#7]-2-[#6]-[#6]-[#6]-[#6]-[#6]-2)cc1 Show InChI InChI=1S/C33H37NO2/c1-22(2)24(4)26-10-13-30-32(20-26)31(21-27-19-28(35)18-23(3)33(27)30)25-8-11-29(12-9-25)36-17-16-34-14-6-5-7-15-34/h8-13,18-21,35H,5-7,14-17H2,1-4H3 | PDB
UniProtKB/SwissProt
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GoogleScholar
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| CHEMBL
PC cid
PC sid
UniChem
Patents
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| Article
PubMed
| 200 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126770
(7-(1,2-Dimethyl-propenyl)-4-methyl-9-[4-(2-piperid...)Show SMILES [#6]\[#6](-[#6])=[#6](\[#6])-c1ccc2c(c1)c(cc1cc(-[#8])cc(-[#6])c21)-c1ccc(-[#8]-[#6]-[#6]-[#7]-2-[#6]-[#6]-[#6]-[#6]-[#6]-2)cc1 Show InChI InChI=1S/C33H37NO2/c1-22(2)24(4)26-10-13-30-32(20-26)31(21-27-19-28(35)18-23(3)33(27)30)25-8-11-29(12-9-25)36-17-16-34-14-6-5-7-15-34/h8-13,18-21,35H,5-7,14-17H2,1-4H3 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| 210 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126772
(7-Isopropenyl-4-methyl-9-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(=C)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C31H33NO2/c1-21(2)24-9-12-28-30(19-24)29(20-25-18-26(33)17-22(3)31(25)28)23-7-10-27(11-8-23)34-16-15-32-13-5-4-6-14-32/h7-12,17-20,33H,1,4-6,13-16H2,2-3H3 | PDB
UniProtKB/SwissProt
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GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
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| Article
PubMed
| 290 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126768
(1-{7-Hydroxy-5-methyl-10-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(C)C(=O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C32H35NO3/c1-21(2)32(35)24-9-12-28-30(19-24)29(20-25-18-26(34)17-22(3)31(25)28)23-7-10-27(11-8-23)36-16-15-33-13-5-4-6-14-33/h7-12,17-21,34H,4-6,13-16H2,1-3H3 | PDB
UniProtKB/SwissProt
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GoogleScholar
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| CHEMBL
PC cid
PC sid
UniChem
Patents
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| Article
PubMed
| 490 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126771
(1-{7-Hydroxy-5-methyl-10-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(=O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H31NO3/c1-20-16-25(33)17-24-19-28(29-18-23(21(2)32)8-11-27(29)30(20)24)22-6-9-26(10-7-22)34-15-14-31-12-4-3-5-13-31/h6-11,16-19,33H,3-5,12-15H2,1-2H3 | PDB
UniProtKB/SwissProt
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GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
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| Article
PubMed
| 630 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor
(Homo sapiens (Human)) | BDBM50126771
(1-{7-Hydroxy-5-methyl-10-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(=O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C30H31NO3/c1-20-16-25(33)17-24-19-28(29-18-23(21(2)32)8-11-27(29)30(20)24)22-6-9-26(10-7-22)34-15-14-31-12-4-3-5-13-31/h6-11,16-19,33H,3-5,12-15H2,1-2H3 | PDB
UniProtKB/SwissProt
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AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor alpha |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Estrogen receptor beta
(Homo sapiens (Human)) | BDBM50126768
(1-{7-Hydroxy-5-methyl-10-[4-(2-piperidin-1-yl-etho...)Show SMILES CC(C)C(=O)c1ccc2c(c1)c(cc1cc(O)cc(C)c21)-c1ccc(OCCN2CCCCC2)cc1 Show InChI InChI=1S/C32H35NO3/c1-21(2)32(35)24-9-12-28-30(19-24)29(20-25-18-26(34)17-22(3)31(25)28)23-7-10-27(11-8-23)36-16-15-33-13-5-4-6-14-33/h7-12,17-21,34H,4-6,13-16H2,1-3H3 | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
SignalGene Inc.
Curated by ChEMBL
| Assay Description
In vitro displacement of 0.5 nM [3H]17-beta-estradiol from human Estrogen receptor beta |
J Med Chem 46: 1408-18 (2003)
Article DOI: 10.1021/jm020536q
BindingDB Entry DOI: 10.7270/Q20R9Q5J |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM4622
(3-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol | An...)Show InChI InChI=1S/C16H15N3O3/c1-21-14-7-12-13(8-15(14)22-2)17-9-18-16(12)19-10-4-3-5-11(20)6-10/h3-9,20H,1-2H3,(H,17,18,19) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM39299
(3-imidazol-1-ylpropyl(7H-purin-6-yl)amine | CHEMBL...)Show InChI InChI=1S/C11H13N7/c1(4-18-5-3-12-8-18)2-13-10-9-11(15-6-14-9)17-7-16-10/h3,5-8H,1-2,4H2,(H2,13,14,15,16,17) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 5.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM13336
(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1 Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 7.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM4621
(Anilinoquinazoline deriv. 4 | CHEMBL150315 | N-(4-...)Show InChI InChI=1S/C16H13ClFN3O2/c1-22-14-6-10-13(7-15(14)23-2)19-8-20-16(10)21-12-4-3-9(17)5-11(12)18/h3-8H,1-2H3,(H,19,20,21) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 8.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3032
(CHEMBL1204168 | CHEMBL29197 | N-(3-bromophenyl)-6,...)Show InChI InChI=1S/C16H14BrN3O2/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-4-10(17)6-11/h3-9H,1-2H3,(H,18,19,20) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.02E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3570
(8-[(3-Bromophenyl)amino]-1H-imidazo[4,5-g]quinazol...)Show InChI InChI=1S/C15H10BrN5/c16-9-2-1-3-10(4-9)21-15-11-5-13-14(19-7-18-13)6-12(11)17-8-20-15/h1-8H,(H,18,19)(H,17,20,21) | PDB
MMDB
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KEGG
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| Article
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| n/a | n/a | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50111603
(3-(4-(dimethylamino)benzylidene)indolin-2-one | 3-...)Show InChI InChI=1S/C17H16N2O/c1-19(2)13-9-7-12(8-10-13)11-15-14-5-3-4-6-16(14)18-17(15)20/h3-11H,1-2H3,(H,18,20)/b15-11+ | PDB
MMDB
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KEGG
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| Article
PubMed
| n/a | n/a | 2.75E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3540
(4-N-(3-bromophenyl)-7-N-methylquinazoline-4,7-diam...)Show InChI InChI=1S/C15H13BrN4/c1-17-11-5-6-13-14(8-11)18-9-19-15(13)20-12-4-2-3-10(16)7-12/h2-9,17H,1H3,(H,18,19,20) | PDB
MMDB
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KEGG
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GoogleScholar
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| CHEMBL
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UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166041
(2-(4-Hydroxy-phenylamino)-[1,4]naphthoquinone | CH...)Show InChI InChI=1S/C16H11NO3/c18-11-7-5-10(6-8-11)17-14-9-15(19)12-3-1-2-4-13(12)16(14)20/h1-8,18H,9H2 | PDB
MMDB
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| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50142887
(1-(tert-butyl)-3-(4-chlorophenyl)-4-aminopyrazolo[...)Show InChI InChI=1S/C15H16ClN5/c1-15(2,3)21-14-11(13(17)18-8-19-14)12(20-21)9-4-6-10(16)7-5-9/h4-8H,1-3H3,(H2,17,18,19) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 5.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166045
(3-(4-Chloro-phenyl)-1-[2-(5-fluoro-2-methyl-1H-ind...)Show SMILES Cc1[nH]c2ccc(F)cc2c1CCN(Cc1ccncc1)C(=S)Nc1ccc(Cl)cc1 Show InChI InChI=1S/C24H22ClFN4S/c1-16-21(22-14-19(26)4-7-23(22)28-16)10-13-30(15-17-8-11-27-12-9-17)24(31)29-20-5-2-18(25)3-6-20/h2-9,11-12,14,28H,10,13,15H2,1H3,(H,29,31) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 6.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50095227
((6,7-Dimethoxy-quinazolin-4-yl)-(4-phenoxy-phenyl)...)Show InChI InChI=1S/C22H19N3O3/c1-26-20-12-18-19(13-21(20)27-2)23-14-24-22(18)25-15-8-10-17(11-9-15)28-16-6-4-3-5-7-16/h3-14H,1-2H3,(H,23,24,25) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 8.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166044
(4-Chloro-N-(2-phenyl-imidazo[1,2-a]pyrimidin-3-yl)...)Show InChI InChI=1S/C19H13ClN4O/c20-15-9-7-14(8-10-15)18(25)23-17-16(13-5-2-1-3-6-13)22-19-21-11-4-12-24(17)19/h1-12H,(H,23,25) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 8.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166036
(CHEMBL192044 | N-{5-[1-(2-Amino-4-methyl-thiazol-5...)Show SMILES CC(=NNC(=O)c1sc(NS(=O)(=O)c2ccccc2)nc1C)c1sc(N)nc1C |w:2.2| Show InChI InChI=1S/C17H18N6O3S3/c1-9-13(27-16(18)19-9)11(3)21-22-15(24)14-10(2)20-17(28-14)23-29(25,26)12-7-5-4-6-8-12/h4-8H,1-3H3,(H2,18,19)(H,20,23)(H,22,24) | PDB
MMDB
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KEGG
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| Article
PubMed
| n/a | n/a | 9.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166038
(3-(4-Fluoro-phenyl)-1-[2-(2-methyl-1H-indol-3-yl)-...)Show SMILES Cc1[nH]c2ccccc2c1CCN(Cc1ccncc1)C(=S)Nc1ccc(F)cc1 Show InChI InChI=1S/C24H23FN4S/c1-17-21(22-4-2-3-5-23(22)27-17)12-15-29(16-18-10-13-26-14-11-18)24(30)28-20-8-6-19(25)7-9-20/h2-11,13-14,27H,12,15-16H2,1H3,(H,28,30) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.04E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166039
((9H-Purin-6-yl)-pyridin-2-ylmethyl-amine | CHEMBL3...)Show InChI InChI=1S/C11H10N6/c1-2-4-12-8(3-1)5-13-10-9-11(15-6-14-9)17-7-16-10/h1-4,6-7H,5H2,(H2,13,14,15,16,17) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.06E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50154227
(6,7-Dimethoxy-2-phenyl-quinoxaline | 6,7-dimethoxy...)Show InChI InChI=1S/C16H14N2O2/c1-19-15-8-12-13(9-16(15)20-2)18-14(10-17-12)11-6-4-3-5-7-11/h3-10H,1-2H3 | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.10E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166046
(CHEMBL191636 | N-(2-Methoxy-phenyl)-2-(5-methyl-5H...)Show InChI InChI=1S/C19H17N5O2S/c1-24-14-9-5-3-7-12(14)17-18(24)21-19(23-22-17)27-11-16(25)20-13-8-4-6-10-15(13)26-2/h3-10H,11H2,1-2H3,(H,20,25) | PDB
MMDB
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| Article
PubMed
| n/a | n/a | 1.36E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM31826
(4-aminoquinazoline, 2a | BMC163482 Compound 3 | CH...)Show InChI InChI=1S/C17H15BrN4O/c1-2-16(23)21-13-6-7-15-14(9-13)17(20-10-19-15)22-12-5-3-4-11(18)8-12/h3-10H,2H2,1H3,(H,21,23)(H,19,20,22) | PDB
MMDB
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KEGG
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| Article
PubMed
| n/a | n/a | 1.80E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166047
(3-[3-(2-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-N-(3...)Show InChI InChI=1S/C17H22FN3O3/c1-12(2)23-11-5-10-19-15(22)8-9-16-20-17(21-24-16)13-6-3-4-7-14(13)18/h3-4,6-7,12H,5,8-11H2,1-2H3,(H,19,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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| Article
PubMed
| n/a | n/a | 2.01E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166042
(5-[1-(3,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-2-(4...)Show SMILES COc1ccc(C=C2SC(Nc3ccc(O)cc3)=NC2=O)cc1OC |w:6.5,c:18| Show InChI InChI=1S/C18H16N2O4S/c1-23-14-8-3-11(9-15(14)24-2)10-16-17(22)20-18(25-16)19-12-4-6-13(21)7-5-12/h3-10,21H,1-2H3,(H,19,20,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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GoogleScholar
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| CHEMBL
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PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.20E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166037
(5-[1-Furan-2-yl-meth-(Z)-ylidene]-2-(4-methoxy-phe...)Show SMILES COc1ccc(NC2=NC(=O)C(S2)=Cc2ccco2)cc1 |w:13.14,t:7| Show InChI InChI=1S/C15H12N2O3S/c1-19-11-6-4-10(5-7-11)16-15-17-14(18)13(21-15)9-12-3-2-8-20-12/h2-9H,1H3,(H,16,17,18) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.30E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50166043
(3-(4-Methoxy-phenyl)-1-[2-(2-methyl-1H-indol-3-yl)...)Show SMILES COc1ccc(NC(=S)N(CCc2c(C)[nH]c3ccccc23)Cc2ccncc2)cc1 Show InChI InChI=1S/C25H26N4OS/c1-18-22(23-5-3-4-6-24(23)27-18)13-16-29(17-19-11-14-26-15-12-19)25(31)28-20-7-9-21(30-2)10-8-20/h3-12,14-15,27H,13,16-17H2,1-2H3,(H,28,31) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Inhibition of EPH receptor B2 using ELISA |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3540
(4-N-(3-bromophenyl)-7-N-methylquinazoline-4,7-diam...)Show InChI InChI=1S/C15H13BrN4/c1-17-11-5-6-13-14(8-11)18-9-19-15(13)20-12-4-2-3-10(16)7-12/h2-9,17H,1H3,(H,18,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | 2.19E+4 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM13336
(4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-...)Show SMILES CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1 Show InChI InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 6.80E+3 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM4622
(3-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol | An...)Show InChI InChI=1S/C16H15N3O3/c1-21-14-7-12-13(8-15(14)22-2)17-9-18-16(12)19-10-4-3-5-11(20)6-10/h3-9,20H,1-2H3,(H,17,18,19) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 2.40E+3 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50142887
(1-(tert-butyl)-3-(4-chlorophenyl)-4-aminopyrazolo[...)Show InChI InChI=1S/C15H16ClN5/c1-15(2,3)21-14-11(13(17)18-8-19-14)12(20-21)9-4-6-10(16)7-5-9/h4-8H,1-3H3,(H2,17,18,19) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 3.65E+4 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3570
(8-[(3-Bromophenyl)amino]-1H-imidazo[4,5-g]quinazol...)Show InChI InChI=1S/C15H10BrN5/c16-9-2-1-3-10(4-9)21-15-11-5-13-14(19-7-18-13)6-12(11)17-8-20-15/h1-8H,(H,18,19)(H,17,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 1.52E+4 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50111603
(3-(4-(dimethylamino)benzylidene)indolin-2-one | 3-...)Show InChI InChI=1S/C17H16N2O/c1-19(2)13-9-7-12(8-10-13)11-15-14-5-3-4-6-16(14)18-17(15)20/h3-11H,1-2H3,(H,18,20)/b15-11+ | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 1.95E+4 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM3032
(CHEMBL1204168 | CHEMBL29197 | N-(3-bromophenyl)-6,...)Show InChI InChI=1S/C16H14BrN3O2/c1-21-14-7-12-13(8-15(14)22-2)18-9-19-16(12)20-11-5-3-4-10(17)6-11/h3-9H,1-2H3,(H,18,19,20) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 8.10E+3 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM4621
(Anilinoquinazoline deriv. 4 | CHEMBL150315 | N-(4-...)Show InChI InChI=1S/C16H13ClFN3O2/c1-22-14-6-10-13(7-15(14)23-2)19-8-20-16(10)21-12-4-3-9(17)5-11(12)18/h3-8H,1-2H3,(H,19,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 6.20E+3 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
Ephrin type-B receptor 2
(Homo sapiens (Human)) | BDBM50095227
((6,7-Dimethoxy-quinazolin-4-yl)-(4-phenoxy-phenyl)...)Show InChI InChI=1S/C22H19N3O3/c1-26-20-12-18-19(13-21(20)27-2)23-14-24-22(18)25-15-8-10-17(11-9-15)28-16-6-4-3-5-7-16/h3-14H,1-2H3,(H,23,24,25) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | n/a | 5.84E+4 | n/a | n/a | n/a | n/a | n/a |
Protana Inc.
Curated by ChEMBL
| Assay Description
Equilibrium binding constant for EPH receptor B2 |
J Med Chem 48: 3221-30 (2005)
Article DOI: 10.1021/jm0492204
BindingDB Entry DOI: 10.7270/Q2DF6QRN |
More data for this
Ligand-Target Pair | |
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