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Compile Data Set for Download or QSAR

Found 72 hits of ic50 data for polymerid = 50006195   
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
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249568
PNG
(CHEMBL4068269)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)C(CC1CCN(Cc2ccccc2)CC1)NC(=O)OCC1c2ccccc2-c2ccccc12
Show InChI InChI=1S/C47H60N4O5/c1-4-7-29-55-45-32-37(54-30-15-26-50(5-2)6-3)22-23-43(45)48-46(52)44(31-35-24-27-51(28-25-35)33-36-16-9-8-10-17-36)49-47(53)56-34-42-40-20-13-11-18-38(40)39-19-12-14-21-41(39)42/h8-14,16-23,32,35,42,44H,4-7,15,24-31,33-34H2,1-3H3,(H,48,52)(H,49,53)
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of CML binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249569
PNG
(CHEMBL4063487)
Show SMILES CCCCn1c(nc2cc(OCCCN(CC)CC)ccc12)[C@@H](Cc1ccc(OCCc2ccc(Cl)cc2)cc1)NC(=O)OC(C)(C)C |r|
Show InChI InChI=1S/C39H53ClN4O4/c1-7-10-24-44-36-21-20-33(46-25-11-23-43(8-2)9-3)28-34(36)41-37(44)35(42-38(45)48-39(4,5)6)27-30-14-18-32(19-15-30)47-26-22-29-12-16-31(40)17-13-29/h12-21,28,35H,7-11,22-27H2,1-6H3,(H,42,45)/t35-/m1/s1
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of S110B binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249569
PNG
(CHEMBL4063487)
Show SMILES CCCCn1c(nc2cc(OCCCN(CC)CC)ccc12)[C@@H](Cc1ccc(OCCc2ccc(Cl)cc2)cc1)NC(=O)OC(C)(C)C |r|
Show InChI InChI=1S/C39H53ClN4O4/c1-7-10-24-44-36-21-20-33(46-25-11-23-43(8-2)9-3)28-34(36)41-37(44)35(42-38(45)48-39(4,5)6)27-30-14-18-32(19-15-30)47-26-22-29-12-16-31(40)17-13-29/h12-21,28,35H,7-11,22-27H2,1-6H3,(H,42,45)/t35-/m1/s1
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249569
PNG
(CHEMBL4063487)
Show SMILES CCCCn1c(nc2cc(OCCCN(CC)CC)ccc12)[C@@H](Cc1ccc(OCCc2ccc(Cl)cc2)cc1)NC(=O)OC(C)(C)C |r|
Show InChI InChI=1S/C39H53ClN4O4/c1-7-10-24-44-36-21-20-33(46-25-11-23-43(8-2)9-3)28-34(36)41-37(44)35(42-38(45)48-39(4,5)6)27-30-14-18-32(19-15-30)47-26-22-29-12-16-31(40)17-13-29/h12-21,28,35H,7-11,22-27H2,1-6H3,(H,42,45)/t35-/m1/s1
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of CML binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249568
PNG
(CHEMBL4068269)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)C(CC1CCN(Cc2ccccc2)CC1)NC(=O)OCC1c2ccccc2-c2ccccc12
Show InChI InChI=1S/C47H60N4O5/c1-4-7-29-55-45-32-37(54-30-15-26-50(5-2)6-3)22-23-43(45)48-46(52)44(31-35-24-27-51(28-25-35)33-36-16-9-8-10-17-36)49-47(53)56-34-42-40-20-13-11-18-38(40)39-19-12-14-21-41(39)42/h8-14,16-23,32,35,42,44H,4-7,15,24-31,33-34H2,1-3H3,(H,48,52)(H,49,53)
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249568
PNG
(CHEMBL4068269)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)C(CC1CCN(Cc2ccccc2)CC1)NC(=O)OCC1c2ccccc2-c2ccccc12
Show InChI InChI=1S/C47H60N4O5/c1-4-7-29-55-45-32-37(54-30-15-26-50(5-2)6-3)22-23-43(45)48-46(52)44(31-35-24-27-51(28-25-35)33-36-16-9-8-10-17-36)49-47(53)56-34-42-40-20-13-11-18-38(40)39-19-12-14-21-41(39)42/h8-14,16-23,32,35,42,44H,4-7,15,24-31,33-34H2,1-3H3,(H,48,52)(H,49,53)
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n/an/a<500n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of S110B binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402568
PNG
(CHEMBL2205566)
Show SMILES CCCCc1sc(Nc2ccc(OCCCN(CC)CC)cc2)nc1-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C32H38ClN3O2S/c1-4-7-9-30-31(24-10-16-28(17-11-24)38-29-18-12-25(33)13-19-29)35-32(39-30)34-26-14-20-27(21-15-26)37-23-8-22-36(5-2)6-3/h10-21H,4-9,22-23H2,1-3H3,(H,34,35)
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n/an/a 550n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402572
PNG
(CHEMBL2205559)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCC2CCCN(CC)C2)cc1
Show InChI InChI=1S/C33H37ClN2O2S/c1-3-5-8-31-32(25-9-17-29(18-10-25)38-30-19-13-27(34)14-20-30)35-33(39-31)26-11-15-28(16-12-26)37-23-24-7-6-21-36(4-2)22-24/h9-20,24H,3-8,21-23H2,1-2H3
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n/an/a 660n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402565
PNG
(CHEMBL2205572)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCN2CCCC2)cc1
Show InChI InChI=1S/C31H33ClN2O2S/c1-2-3-6-29-30(23-7-15-27(16-8-23)36-28-17-11-25(32)12-18-28)33-31(37-29)24-9-13-26(14-10-24)35-22-21-34-19-4-5-20-34/h7-18H,2-6,19-22H2,1H3
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n/an/a 910n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402564
PNG
(CHEMBL2205549)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCN2CCCCC2)cc1
Show InChI InChI=1S/C32H35ClN2O2S/c1-2-3-7-30-31(24-8-16-28(17-9-24)37-29-18-12-26(33)13-19-29)34-32(38-30)25-10-14-27(15-11-25)36-23-22-35-20-5-4-6-21-35/h8-19H,2-7,20-23H2,1H3
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n/an/a 1.04E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402575
PNG
(CHEMBL2205556)
Show SMILES CCCCc1sc(nc1-c1ccc(OCCCN(CC)CC)cc1)-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C32H37ClN2O2S/c1-4-7-9-30-31(24-10-16-27(17-11-24)36-23-8-22-35(5-2)6-3)34-32(38-30)25-12-18-28(19-13-25)37-29-20-14-26(33)15-21-29/h10-21H,4-9,22-23H2,1-3H3
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n/an/a 1.12E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402570
PNG
(CHEMBL2205561)
Show SMILES CCCCc1nc(sc1-c1ccc(OCC2CCCN(CC)C2)cc1)-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C33H37ClN2O2S/c1-3-5-8-31-32(25-9-15-28(16-10-25)37-23-24-7-6-21-36(4-2)22-24)39-33(35-31)26-11-17-29(18-12-26)38-30-19-13-27(34)14-20-30/h9-20,24H,3-8,21-23H2,1-2H3
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n/an/a 1.14E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402563
PNG
(CHEMBL2205550)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCN2CCN(C)CC2)cc1
Show InChI InChI=1S/C32H36ClN3O2S/c1-3-4-5-30-31(24-6-14-28(15-7-24)38-29-16-10-26(33)11-17-29)34-32(39-30)25-8-12-27(13-9-25)37-23-22-36-20-18-35(2)19-21-36/h6-17H,3-5,18-23H2,1-2H3
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n/an/a 1.21E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402566
PNG
(CHEMBL2205569)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCCN2CCN(C)CC2)cc1
Show InChI InChI=1S/C33H38ClN3O2S/c1-3-4-6-31-32(25-7-15-29(16-8-25)39-30-17-11-27(34)12-18-30)35-33(40-31)26-9-13-28(14-10-26)38-24-5-19-37-22-20-36(2)21-23-37/h7-18H,3-6,19-24H2,1-2H3
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n/an/a 1.24E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402561
PNG
(CHEMBL2205553)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCN(CC)CC)cc1
Show InChI InChI=1S/C31H35ClN2O2S/c1-4-7-8-29-30(23-9-17-27(18-10-23)36-28-19-13-25(32)14-20-28)33-31(37-29)24-11-15-26(16-12-24)35-22-21-34(5-2)6-3/h9-20H,4-8,21-22H2,1-3H3
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n/an/a 1.58E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402573
PNG
(CHEMBL2205558)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCCN(CC)CC)cc1
Show InChI InChI=1S/C32H37ClN2O2S/c1-4-7-9-30-31(24-10-18-28(19-11-24)37-29-20-14-26(33)15-21-29)34-32(38-30)25-12-16-27(17-13-25)36-23-8-22-35(5-2)6-3/h10-21H,4-9,22-23H2,1-3H3
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n/an/a 1.72E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249578
PNG
(CHEMBL4095634)
Show SMILES CCCCOc1cc(ccc1NC(=O)[C@H](N)Cc1ccc2ccccc2c1)C(=O)OCCN(CC)CC |r|
Show InChI InChI=1S/C30H39N3O4/c1-4-7-17-36-28-21-25(30(35)37-18-16-33(5-2)6-3)14-15-27(28)32-29(34)26(31)20-22-12-13-23-10-8-9-11-24(23)19-22/h8-15,19,21,26H,4-7,16-18,20,31H2,1-3H3,(H,32,34)/t26-/m1/s1
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n/an/a 1.75E+3n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of S110B binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402567
PNG
(CHEMBL2205568)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCCN2CCCCC2)cc1
Show InChI InChI=1S/C33H37ClN2O2S/c1-2-3-8-31-32(25-9-17-29(18-10-25)38-30-19-13-27(34)14-20-30)35-33(39-31)26-11-15-28(16-12-26)37-24-7-23-36-21-5-4-6-22-36/h9-20H,2-8,21-24H2,1H3
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n/an/a 1.84E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005634
PNG
(CHEMBL3235375)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccc(F)cc2)cc1
Show InChI InChI=1S/C34H41FN4O4/c1-5-8-21-42-33-23-29(41-22-9-20-39(6-2)7-3)18-19-30(33)36-34(40)32-24-31(37-38(32)4)25-10-14-27(15-11-25)43-28-16-12-26(35)13-17-28/h10-19,23-24H,5-9,20-22H2,1-4H3,(H,36,40)
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n/an/a 1.90E+3n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to biotin-labeled human RAGE domain V after 60 mins by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005633
PNG
(CHEMBL3235374)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccc(cc2)C(F)(F)F)cc1
Show InChI InChI=1S/C35H41F3N4O4/c1-5-8-21-45-33-23-29(44-22-9-20-42(6-2)7-3)18-19-30(33)39-34(43)32-24-31(40-41(32)4)25-10-14-27(15-11-25)46-28-16-12-26(13-17-28)35(36,37)38/h10-19,23-24H,5-9,20-22H2,1-4H3,(H,39,43)
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n/an/a 1.90E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005634
PNG
(CHEMBL3235375)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccc(F)cc2)cc1
Show InChI InChI=1S/C34H41FN4O4/c1-5-8-21-42-33-23-29(41-22-9-20-39(6-2)7-3)18-19-30(33)36-34(40)32-24-31(37-38(32)4)25-10-14-27(15-11-25)43-28-16-12-26(35)13-17-28/h10-19,23-24H,5-9,20-22H2,1-4H3,(H,36,40)
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n/an/a 1.90E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402574
PNG
(CHEMBL2205557)
Show SMILES CCCCc1sc(nc1-c1ccc(OCC2CCCN(CC)C2)cc1)-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C33H37ClN2O2S/c1-3-5-8-31-32(25-9-15-28(16-10-25)37-23-24-7-6-21-36(4-2)22-24)35-33(39-31)26-11-17-29(18-12-26)38-30-19-13-27(34)14-20-30/h9-20,24H,3-8,21-23H2,1-2H3
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n/an/a 1.91E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402571
PNG
(CHEMBL2205560)
Show SMILES CCCCc1nc(sc1-c1ccc(OCCCN(CC)CC)cc1)-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C32H37ClN2O2S/c1-4-7-9-30-31(24-10-16-27(17-11-24)36-23-8-22-35(5-2)6-3)38-32(34-30)25-12-18-28(19-13-25)37-29-20-14-26(33)15-21-29/h10-21H,4-9,22-23H2,1-3H3
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n/an/a 2.01E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249578
PNG
(CHEMBL4095634)
Show SMILES CCCCOc1cc(ccc1NC(=O)[C@H](N)Cc1ccc2ccccc2c1)C(=O)OCCN(CC)CC |r|
Show InChI InChI=1S/C30H39N3O4/c1-4-7-17-36-28-21-25(30(35)37-18-16-33(5-2)6-3)14-15-27(28)32-29(34)26(31)20-22-12-13-23-10-8-9-11-24(23)19-22/h8-15,19,21,26H,4-7,16-18,20,31H2,1-3H3,(H,32,34)/t26-/m1/s1
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n/an/a 2.29E+3n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of CML binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005629
PNG
(CHEMBL3235049)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(OC2CCCCC2)cc1
Show InChI InChI=1S/C34H48N4O4/c1-5-8-22-41-33-24-29(40-23-12-21-38(6-2)7-3)19-20-30(33)35-34(39)32-25-31(36-37(32)4)26-15-17-28(18-16-26)42-27-13-10-9-11-14-27/h15-20,24-25,27H,5-14,21-23H2,1-4H3,(H,35,39)
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n/an/a 2.50E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402562
PNG
(CHEMBL2205552)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCN(C)C)cc1
Show InChI InChI=1S/C29H31ClN2O2S/c1-4-5-6-27-28(21-7-15-25(16-8-21)34-26-17-11-23(30)12-18-26)31-29(35-27)22-9-13-24(14-10-22)33-20-19-32(2)3/h7-18H,4-6,19-20H2,1-3H3
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n/an/a 3.18E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249578
PNG
(CHEMBL4095634)
Show SMILES CCCCOc1cc(ccc1NC(=O)[C@H](N)Cc1ccc2ccccc2c1)C(=O)OCCN(CC)CC |r|
Show InChI InChI=1S/C30H39N3O4/c1-4-7-17-36-28-21-25(30(35)37-18-16-33(5-2)6-3)14-15-27(28)32-29(34)26(31)20-22-12-13-23-10-8-9-11-24(23)19-22/h8-15,19,21,26H,4-7,16-18,20,31H2,1-3H3,(H,32,34)/t26-/m1/s1
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n/an/a 3.40E+3n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to RAGE (unknown origin) by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605302
PNG
(CHEMBL5191418)
Show SMILES CCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 3.49E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605310
PNG
(CHEMBL5194592)
Show SMILES CCCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(Cc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 4.04E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605284
PNG
(CHEMBL5170867)
Show SMILES CCCCn1nc(cc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 4.15E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50397837
PNG
(CHEMBL2179074)
Show SMILES CCN(CC)CCOc1ccccc1Nc1nc(cc(n1)-c1ccc(Cl)cc1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C28H28Cl2N4O/c1-3-34(4-2)17-18-35-27-8-6-5-7-24(27)31-28-32-25(20-9-13-22(29)14-10-20)19-26(33-28)21-11-15-23(30)16-12-21/h5-16,19H,3-4,17-18H2,1-2H3,(H,31,32,33)
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n/an/a 4.60E+3n/an/an/an/an/an/a



Seoul National University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant biotinylated receptor for advanced glycation end product expressed in Escherichia coli DE3 assessed as inhibition of ...


J Med Chem 55: 9120-35 (2012)


Article DOI: 10.1021/jm300172z
BindingDB Entry DOI: 10.7270/Q289170G
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005635
PNG
(CHEMBL3235378)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccc(Cl)c(OC)c2)cc1
Show InChI InChI=1S/C35H43ClN4O5/c1-6-9-20-44-34-22-27(43-21-10-19-40(7-2)8-3)16-18-30(34)37-35(41)32-24-31(38-39(32)4)25-11-13-26(14-12-25)45-28-15-17-29(36)33(23-28)42-5/h11-18,22-24H,6-10,19-21H2,1-5H3,(H,37,41)
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n/an/a 5.30E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005630
PNG
(CHEMBL3235050)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccccc2)cc1
Show InChI InChI=1S/C34H42N4O4/c1-5-8-22-41-33-24-29(40-23-12-21-38(6-2)7-3)19-20-30(33)35-34(39)32-25-31(36-37(32)4)26-15-17-28(18-16-26)42-27-13-10-9-11-14-27/h9-11,13-20,24-25H,5-8,12,21-23H2,1-4H3,(H,35,39)
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n/an/a 5.40E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50402569
PNG
(CHEMBL2205565)
Show SMILES CCCCc1sc(NC(=O)c2ccc(OCCCN(CC)CC)cc2)nc1-c1ccc(Oc2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C33H38ClN3O3S/c1-4-7-9-30-31(24-10-18-28(19-11-24)40-29-20-14-26(34)15-21-29)35-33(41-30)36-32(38)25-12-16-27(17-13-25)39-23-8-22-37(5-2)6-3/h10-21H,4-9,22-23H2,1-3H3,(H,35,36,38)
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n/an/a 5.59E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Antagonist activity at human biotinylated RAGE assessed as inhibition of amyloid beta binding after 60 mins by ELISA


Bioorg Med Chem Lett 22: 7555-61 (2012)


Article DOI: 10.1016/j.bmcl.2012.10.022
BindingDB Entry DOI: 10.7270/Q2XG9S9S
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605313
PNG
(CHEMBL5180815)
Show SMILES CCCCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2cn(C)c3ccc(cc23)C#N)CC1
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n/an/a 6.03E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005632
PNG
(CHEMBL3235052)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccc(OC)cc2)cc1
Show InChI InChI=1S/C35H44N4O5/c1-6-9-22-43-34-24-30(42-23-10-21-39(7-2)8-3)19-20-31(34)36-35(40)33-25-32(37-38(33)4)26-11-13-28(14-12-26)44-29-17-15-27(41-5)16-18-29/h11-20,24-25H,6-10,21-23H2,1-5H3,(H,36,40)
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n/an/a 7.80E+3n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605294
PNG
(CHEMBL5203206)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2cn(C)c3ccc(cc23)C#N)CC1
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n/an/a 8.26E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605307
PNG
(CHEMBL5175011)
Show SMILES Clc1ccc(Oc2ccc(cc2)-n2cc(nc2C2CCC2)C2CCN(CCCCc3c[nH]c4ccc(cc34)C#N)CC2)cc1
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n/an/a 8.29E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50397836
PNG
(CHEMBL2179073)
Show SMILES CCN(CC)CCOc1cccc(Nc2nc(cc(n2)-c2ccc(Cl)cc2)-c2ccc(Cl)cc2)c1
Show InChI InChI=1S/C28H28Cl2N4O/c1-3-34(4-2)16-17-35-25-7-5-6-24(18-25)31-28-32-26(20-8-12-22(29)13-9-20)19-27(33-28)21-10-14-23(30)15-11-21/h5-15,18-19H,3-4,16-17H2,1-2H3,(H,31,32,33)
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n/an/a 1.05E+4n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605303
PNG
(CHEMBL5208902)
Show SMILES CCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 1.25E+4n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605283
PNG
(CHEMBL5188606)
Show SMILES CCCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 1.29E+4n/an/an/an/an/an/a


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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249580
PNG
(Azeliragon | PF-04494700 | TTP448 | US11524942, Co...)
Show SMILES CCCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)-c1ccc(OCCCN(CC)CC)cc1
Show InChI InChI=1S/C32H38ClN3O2/c1-4-7-9-32-34-31(25-10-16-28(17-11-25)37-23-8-22-35(5-2)6-3)24-36(32)27-14-20-30(21-15-27)38-29-18-12-26(33)13-19-29/h10-21,24H,4-9,22-23H2,1-3H3
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n/an/a 1.35E+4n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605286
PNG
(CHEMBL5192104)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 1.43E+4n/an/an/an/an/an/a


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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605291
PNG
(CHEMBL5170035)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(Cc2c[nH]c3ccc(cc23)C#N)CC1
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n/an/a 1.61E+4n/an/an/an/an/an/a


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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50397836
PNG
(CHEMBL2179073)
Show SMILES CCN(CC)CCOc1cccc(Nc2nc(cc(n2)-c2ccc(Cl)cc2)-c2ccc(Cl)cc2)c1
Show InChI InChI=1S/C28H28Cl2N4O/c1-3-34(4-2)16-17-35-25-7-5-6-24(18-25)31-28-32-26(20-8-12-22(29)13-9-20)19-27(33-28)21-10-14-23(30)15-11-21/h5-15,18-19H,3-4,16-17H2,1-2H3,(H,31,32,33)
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n/an/a 1.65E+4n/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to biotin-labeled human RAGE domain V after 60 mins by ELISA


J Med Chem 60: 7213-7232 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00058
BindingDB Entry DOI: 10.7270/Q2KD21BP
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50397836
PNG
(CHEMBL2179073)
Show SMILES CCN(CC)CCOc1cccc(Nc2nc(cc(n2)-c2ccc(Cl)cc2)-c2ccc(Cl)cc2)c1
Show InChI InChI=1S/C28H28Cl2N4O/c1-3-34(4-2)16-17-35-25-7-5-6-24(18-25)31-28-32-26(20-8-12-22(29)13-9-20)19-27(33-28)21-10-14-23(30)15-11-21/h5-15,18-19H,3-4,16-17H2,1-2H3,(H,31,32,33)
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n/an/a 1.65E+4n/an/an/an/an/an/a



Seoul National University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant biotinylated receptor for advanced glycation end product expressed in Escherichia coli DE3 assessed as inhibition of ...


J Med Chem 55: 9120-35 (2012)


Article DOI: 10.1021/jm300172z
BindingDB Entry DOI: 10.7270/Q289170G
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50005631
PNG
(CHEMBL3235051)
Show SMILES CCCCOc1cc(OCCCN(CC)CC)ccc1NC(=O)c1cc(nn1C)-c1ccc(Oc2ccccn2)cc1
Show InChI InChI=1S/C33H41N5O4/c1-5-8-21-41-31-23-27(40-22-11-20-38(6-2)7-3)17-18-28(31)35-33(39)30-24-29(36-37(30)4)25-13-15-26(16-14-25)42-32-12-9-10-19-34-32/h9-10,12-19,23-24H,5-8,11,20-22H2,1-4H3,(H,35,39)
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n/an/a 1.89E+4n/an/an/an/an/an/a



Woosuk University

Curated by ChEMBL


Assay Description
Inhibition of biotinylated human RAGE assessed as bound amyloid beta level after 60 mins by ELISA


Eur J Med Chem 79: 128-42 (2014)


Article DOI: 10.1016/j.ejmech.2014.03.072
BindingDB Entry DOI: 10.7270/Q2C82BTF
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605316
PNG
(CHEMBL5178292)
Show SMILES CCCCCc1nc(cn1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2cn(C(C)C)c3ccc(cc23)C#N)CC1
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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605297
PNG
(CHEMBL5172417)
Show SMILES CCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2cn(C)c3ccc(cc23)C#N)CC1
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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50605298
PNG
(CHEMBL5174761)
Show SMILES CCCCc1sc(nc1-c1ccc(Oc2ccc(Cl)cc2)cc1)C1CCN(CCCCc2cn(CC)c3ccc(cc23)C#N)CC1
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Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114347
BindingDB Entry DOI: 10.7270/Q2PG1WTJ
More data for this
Ligand-Target Pair
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