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Compile Data Set for Download or QSAR

Found 84 hits Enz. Inhib. hit(s) with Target = 'Advanced glycosylation end product-specific receptor'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249567
PNG
(CHEMBL4075936)
Show SMILES Clc1ccc(cc1)C(=O)N(Cc1ccccc1)C1CCCCC1
Show InChI InChI=1S/C20H22ClNO/c21-18-13-11-17(12-14-18)20(23)22(19-9-5-2-6-10-19)15-16-7-3-1-4-8-16/h1,3-4,7-8,11-14,19H,2,5-6,9-10,15H2
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25n/an/an/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))
BDBM50249567
PNG
(CHEMBL4075936)
Show SMILES Clc1ccc(cc1)C(=O)N(Cc1ccccc1)C1CCCCC1
Show InChI InChI=1S/C20H22ClNO/c21-18-13-11-17(12-14-18)20(23)22(19-9-5-2-6-10-19)15-16-7-3-1-4-8-16/h1,3-4,7-8,11-14,19H,2,5-6,9-10,15H2
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148n/an/an/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of HMGB1 binding to human RAGE domain V expressed in CHO cells


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))
BDBM50249567
PNG
(CHEMBL4075936)
Show SMILES Clc1ccc(cc1)C(=O)N(Cc1ccccc1)C1CCCCC1
Show InChI InChI=1S/C20H22ClNO/c21-18-13-11-17(12-14-18)20(23)22(19-9-5-2-6-10-19)15-16-7-3-1-4-8-16/h1,3-4,7-8,11-14,19H,2,5-6,9-10,15H2
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230n/an/an/an/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of S110B binding to human RAGE domain V expressed in CHO cells


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
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
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 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 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
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))
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
Displacement of [I125]amyloid beta (1 to 40) from human RAGE domain V expressed in CHO cells


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
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
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 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))
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
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))
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))
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))
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))
BDBM50249575
PNG
(CHEMBL4100986 | US10729695, Compound CB-10)
Show SMILES CC(C)CCC1C(C)=NN(C1=O)c1nc2ccccc2[nH]1
Show InChI InChI=1S/C16H20N4O/c1-10(2)8-9-12-11(3)19-20(15(12)21)16-17-13-6-4-5-7-14(13)18-16/h4-7,10,12H,8-9H2,1-3H3,(H,17,18)
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n/an/an/a 3n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Binding affinity to human RAGE cytoplasmic domain by tryptophan fluorescence assay


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))
BDBM50249576
PNG
(CHEMBL4075539 | US10729695, Compound CD-6)
Show SMILES Cn1c2ccccc2n(CC(O)Cn2c3ccccc3c3ccccc23)c1=O
Show InChI InChI=1S/C23H21N3O2/c1-24-21-12-6-7-13-22(21)26(23(24)28)15-16(27)14-25-19-10-4-2-8-17(19)18-9-3-5-11-20(18)25/h2-13,16,27H,14-15H2,1H3
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n/an/an/a 4n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Binding affinity to human RAGE cytoplasmic domain by tryptophan fluorescence assay


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))
BDBM50249577
PNG
(CHEMBL4072531 | US10729695, Compound CB-4)
Show SMILES OC(Cn1ccc2ccccc12)Cn1cnc2ccccc12
Show InChI InChI=1S/C18H17N3O/c22-15(11-20-10-9-14-5-1-3-7-17(14)20)12-21-13-19-16-6-2-4-8-18(16)21/h1-10,13,15,22H,11-12H2
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n/an/an/a 2n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Binding affinity to human RAGE cytoplasmic domain by tryptophan fluorescence assay


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))
BDBM50249579
PNG
(CHEMBL1477694 | US10729695, Compound CB-3)
Show SMILES Cc1nc2ccccc2n1CC(O)Cn1c2ccccc2c2ccccc12
Show InChI InChI=1S/C23H21N3O/c1-16-24-20-10-4-7-13-23(20)25(16)14-17(27)15-26-21-11-5-2-8-18(21)19-9-3-6-12-22(19)26/h2-13,17,27H,14-15H2,1H3
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n/an/an/a 1n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Binding affinity to human RAGE cytoplasmic domain by tryptophan fluorescence assay


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))
BDBM50249580
PNG
(AZELIRAGON | Azeliragon | PF-04494700 | TTP448)
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/an/a 500n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta (1 to 42) binding to RAGE domain V (unknown origin) by fluorescence polarization assay


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))
BDBM50249581
PNG
(CHEBI:6700 | MATRINE | Matrine)
Show SMILES O=C1CCC[C@@H]2[C@H]3CCCN4CCC[C@@H](CN12)[C@@H]34
Show InChI InChI=1S/C15H24N2O/c18-14-7-1-6-13-12-5-3-9-16-8-2-4-11(15(12)16)10-17(13)14/h11-13,15H,1-10H2/t11-,12+,13+,15-/m0/s1
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n/an/an/a 2.40E+7n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Inhibition of amyloid beta binding to human RAGE domain V (Met1 to Ala 344 residues) expressed in HEK293 cells after 10 mins by MST assay


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))
BDBM50249582
PNG
(CHEMBL1547178 | US10729695, Compound CB-13)
Show SMILES Cc1c(Cl)cccc1NC(=O)CNC(=O)c1ccccc1F
Show InChI InChI=1S/C16H14ClFN2O2/c1-10-12(17)6-4-8-14(10)20-15(21)9-19-16(22)11-5-2-3-7-13(11)18/h2-8H,9H2,1H3,(H,19,22)(H,20,21)
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n/an/an/a 32n/an/an/an/an/a



King's College London

Curated by ChEMBL


Assay Description
Binding affinity to human RAGE cytoplasmic domain by tryptophan fluorescence assay


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))
BDBM453304
PNG
(US10729695, Compound CD-29)
Show SMILES Cc1nccn1CC(O)Cn1c2ccccc2c2ccccc12
Show InChI InChI=1S/C19H19N3O/c1-14-20-10-11-21(14)12-15(23)13-22-18-8-4-2-6-16(18)17-7-3-5-9-19(17)22/h2-11,15,23H,12-13H2,1H3
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US Patent
n/an/an/a 78n/an/an/an/an/a



The Research Foundation for the State University of New York; New York University

US Patent


Assay Description
Day 1Step 1. Add 50 μl anti-mDial (1:160 dilution in 0.1M NaHCO3 pH 9.6)/well. Incubate overnight at 4 C.Day 2Step 2. Use the plate washer to a...


US Patent US10729695 (2020)

More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249574
PNG
(CHEMBL4077165 | US10729695, Compound CB-5)
Show SMILES Oc1cccc(Nc2nc(cs2)-c2ccc(F)cc2F)c1
Show InChI InChI=1S/C15H10F2N2OS/c16-9-4-5-12(13(17)6-9)14-8-21-15(19-14)18-10-2-1-3-11(20)7-10/h1-8,20H,(H,18,19)
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n/an/an/a 1.10n/an/an/an/an/a



The Research Foundation for the State University of New York; New York University

US Patent


Assay Description
Day 1Step 1. Add 50 μl anti-mDial (1:160 dilution in 0.1M NaHCO3 pH 9.6)/well. Incubate overnight at 4 C.Day 2Step 2. Use the plate washer to a...


US Patent US10729695 (2020)

More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM50249571
PNG
(CHEMBL4101927 | US10729695, Compound CB-6)
Show SMILES COc1cc(NC(C)=O)c(Cl)cc1C(=O)Nc1nccs1
Show InChI InChI=1S/C13H12ClN3O3S/c1-7(18)16-10-6-11(20-2)8(5-9(10)14)12(19)17-13-15-3-4-21-13/h3-6H,1-2H3,(H,16,18)(H,15,17,19)
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US Patent
n/an/an/a 0.100n/an/an/an/an/a



The Research Foundation for the State University of New York; New York University

US Patent


Assay Description
Day 1Step 1. Add 50 μl anti-mDial (1:160 dilution in 0.1M NaHCO3 pH 9.6)/well. Incubate overnight at 4 C.Day 2Step 2. Use the plate washer to a...


US Patent US10729695 (2020)

More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM95323
PNG
(4-[4-(2-methoxyphenyl)-6-(trifluoromethyl)-2-pyrim...)
Show SMILES COc1ccccc1-c1cc(nc(n1)N1CCOCC1)C(F)(F)F
Show InChI InChI=1S/C16H16F3N3O2/c1-23-13-5-3-2-4-11(13)12-10-14(16(17,18)19)21-15(20-12)22-6-8-24-9-7-22/h2-5,10H,6-9H2,1H3
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US Patent
n/an/an/a 0.550n/an/an/an/an/a



The Research Foundation for the State University of New York; New York University

US Patent


Assay Description
Day 1Step 1. Add 50 μl anti-mDial (1:160 dilution in 0.1M NaHCO3 pH 9.6)/well. Incubate overnight at 4 C.Day 2Step 2. Use the plate washer to a...


US Patent US10729695 (2020)

More data for this
Ligand-Target Pair
Advanced glycosylation end product-specific receptor


(Homo sapiens (Human))
BDBM453279
PNG
(US10729695, Compound CB-8)
Show SMILES COC(=O)c1cc(OC)c(OC)cc1NC(=O)C1Oc2ccccc2OC1C
Show InChI InChI=1S/C20H21NO7/c1-11-18(28-15-8-6-5-7-14(15)27-11)19(22)21-13-10-17(25-3)16(24-2)9-12(13)20(23)26-4/h5-11,18H,1-4H3,(H,21,22)
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US Patent
n/an/an/a 2n/an/an/an/an/a



The Research Foundation for the State University of New York; New York University

US Patent


Assay Description
Day 1Step 1. Add 50 μl anti-mDial (1:160 dilution in 0.1M NaHCO3 pH 9.6)/well. Incubate overnight at 4 C.Day 2Step 2. Use the plate washer to a...


US Patent US10729695 (2020)

More data for this
Ligand-Target Pair
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