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Compile Data Set for Download or QSAR

Found 3808 hits with Last Name = 'ahn' and Initial = 'k'   
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
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223890
PNG
((S)-3-[3'-(2-cyclopropylamino-3,4-dioxo-cyclobut-1...)
Show SMILES CC1(C)C2CC[C@@]1(C(=O)C2)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(Nc2c(NC3CC3)c(=O)c2=O)c1)C(O)=O
Show InChI InChI=1S/C31H33N3O7S/c1-30(2)20-12-13-31(30,24(35)16-20)42(40,41)34-23(29(38)39)14-17-6-8-18(9-7-17)19-4-3-5-22(15-19)33-26-25(27(36)28(26)37)32-21-10-11-21/h3-9,15,20-21,23,32-34H,10-14,16H2,1-2H3,(H,38,39)/t20?,23-,31-/m0/s1
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0.100n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
Muscarinic acetylcholine receptor M5


(Homo sapiens (Human))
BDBM50403547
PNG
(ATROPEN | ATROPINE)
Show SMILES CN1[C@H]2CC[C@@H]1C[C@@H](C2)OC(=O)C(CO)c1ccccc1
Show InChI InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3/t13-,14+,15+,16?
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0.400n/an/an/an/an/an/an/an/a



University of South Florida

Curated by ChEMBL


Assay Description
Displacement of [3H]QNB from muscarinic acetylcholine M5 receptor after 1.5 hrs by scintillation counting


Bioorg Med Chem 19: 5756-62 (2011)


Article DOI: 10.1016/j.bmc.2011.08.033
BindingDB Entry DOI: 10.7270/Q25X29BF
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223891
PNG
((S)-3-[3'-(2-cyclopropylamino-3,4-dioxo-cyclobut-1...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(Nc2c(NC3CC3)c(=O)c2=O)c1)C(O)=O
Show InChI InChI=1S/C31H31N3O6S/c1-17-13-18(2)30(19(3)14-17)41(39,40)34-25(31(37)38)15-20-7-9-21(10-8-20)22-5-4-6-24(16-22)33-27-26(28(35)29(27)36)32-23-11-12-23/h4-10,13-14,16,23,25,32-34H,11-12,15H2,1-3H3,(H,37,38)/t25-/m0/s1
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0.5n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50108482
PNG
(2-{3-[3'-((R)-2-Carboxy-1-phenyl-ethylsulfamoyl)-4...)
Show SMILES COc1ccc(cc1S(=O)(=O)N[C@H](CC(O)=O)c1ccccc1)-c1cccc(NC(=O)Nc2[nH]c3ccccc3[nH+]2)c1
Show InChI InChI=1S/C30H27N5O6S/c1-41-26-15-14-21(17-27(26)42(39,40)35-25(18-28(36)37)19-8-3-2-4-9-19)20-10-7-11-22(16-20)31-30(38)34-29-32-23-12-5-6-13-24(23)33-29/h2-17,25,35H,18H2,1H3,(H,36,37)(H3,31,32,33,34,38)/p+1/t25-/m1/s1
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0.700n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Displacement of 125-I echistatin from Vitronectin receptor (alpha v beta3)


Bioorg Med Chem Lett 12: 205-8 (2001)


Article DOI: 10.1016/s0960-894x(01)00717-x
BindingDB Entry DOI: 10.7270/Q27945T7
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223897
PNG
((S)-3-{3'-[(1H-imidazole-2-carbonyl)-amino]-biphen...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(NC(=O)c2ncc[nH]2)c1)C(O)=O
Show InChI InChI=1S/C28H28N4O5S/c1-17-13-18(2)25(19(3)14-17)38(36,37)32-24(28(34)35)15-20-7-9-21(10-8-20)22-5-4-6-23(16-22)31-27(33)26-29-11-12-30-26/h4-14,16,24,32H,15H2,1-3H3,(H,29,30)(H,31,33)(H,34,35)/t24-/m0/s1
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1n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125304
PNG
((S)-2-((S)-7,7-Dimethyl-2-oxo-bicyclo[2.2.1]hept-1...)
Show SMILES CCCNC(=O)Nc1cccc(c1)-c1ccc(C[C@H](NS(=O)(=O)C[C@]23CCC(CC2=O)C3(C)C)C(O)=O)cc1
Show InChI InChI=1S/C29H37N3O6S/c1-4-14-30-27(36)31-23-7-5-6-21(16-23)20-10-8-19(9-11-20)15-24(26(34)35)32-39(37,38)18-29-13-12-22(17-25(29)33)28(29,2)3/h5-11,16,22,24,32H,4,12-15,17-18H2,1-3H3,(H,34,35)(H2,30,31,36)/t22?,24-,29+/m0/s1
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1n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223888
PNG
((S)-3-[3'-(4,5-dihydro-1H-imidazol-2-ylamino)-biph...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(c1)N=C1NCCN1)C(O)=O
Show InChI InChI=1S/C27H30N4O4S/c1-17-13-18(2)25(19(3)14-17)36(34,35)31-24(26(32)33)15-20-7-9-21(10-8-20)22-5-4-6-23(16-22)30-27-28-11-12-29-27/h4-10,13-14,16,24,31H,11-12,15H2,1-3H3,(H,32,33)(H2,28,29,30)/t24-/m0/s1
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1.30n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50108460
PNG
(2-{3-[3'-((S)-2-Carboxy-1-phenyl-ethylsulfamoyl)-4...)
Show SMILES COc1ccc(cc1S(=O)(=O)N[C@@H](CC(O)=O)c1ccccc1)-c1cccc(NC(=O)Nc2[nH]c3ccccc3[nH+]2)c1
Show InChI InChI=1S/C30H27N5O6S/c1-41-26-15-14-21(17-27(26)42(39,40)35-25(18-28(36)37)19-8-3-2-4-9-19)20-10-7-11-22(16-20)31-30(38)34-29-32-23-12-5-6-13-24(23)33-29/h2-17,25,35H,18H2,1H3,(H,36,37)(H3,31,32,33,34,38)/p+1/t25-/m0/s1
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1.40n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
In vitro activity in an vitronectin receptor (alpha v beta3) scintillation bead assay using 125-I labelled echistatin as a radioligand


Bioorg Med Chem Lett 12: 205-8 (2001)


Article DOI: 10.1016/s0960-894x(01)00717-x
BindingDB Entry DOI: 10.7270/Q27945T7
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50095296
PNG
(CHEMBL3589082 | US9278953, 1)
Show SMILES CCn1ncc2c(F)cc(cc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C20H21Cl2N5O/c1-26-5-7-27(8-6-26)20-15-9-13(28-2)3-4-14(15)19(24-25-20)10-16-17(21)11-23-12-18(16)22/h3-4,9,11-12H,5-8,10H2,1-2H3
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US Patent
2 -49.7n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125289
PNG
((S)-3-[3'-(3-Cyclopropyl-ureido)-biphenyl-4-yl]-2-...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(NC(=O)NC2CC2)c1)C(O)=O
Show InChI InChI=1S/C28H31N3O5S/c1-17-13-18(2)26(19(3)14-17)37(35,36)31-25(27(32)33)15-20-7-9-21(10-8-20)22-5-4-6-24(16-22)30-28(34)29-23-11-12-23/h4-10,13-14,16,23,25,31H,11-12,15H2,1-3H3,(H,32,33)(H2,29,30,34)/t25-/m0/s1
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2.5n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125289
PNG
((S)-3-[3'-(3-Cyclopropyl-ureido)-biphenyl-4-yl]-2-...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(NC(=O)NC2CC2)c1)C(O)=O
Show InChI InChI=1S/C28H31N3O5S/c1-17-13-18(2)26(19(3)14-17)37(35,36)31-25(27(32)33)15-20-7-9-21(10-8-20)22-5-4-6-24(16-22)30-28(34)29-23-11-12-23/h4-10,13-14,16,23,25,31H,11-12,15H2,1-3H3,(H,32,33)(H2,29,30,34)/t25-/m0/s1
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2.5n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A


(Rattus norvegicus (rat))
BDBM50077661
PNG
(2-{4-[3-(4-Chloro-phenyl)-pyrrolidin-1-yl]-butyl}-...)
Show SMILES Clc1ccc(cc1)C1CCN(CCCCN2C(=O)c3ccccc3S2(=O)=O)C1
Show InChI InChI=1S/C21H23ClN2O3S/c22-18-9-7-16(8-10-18)17-11-14-23(15-17)12-3-4-13-24-21(25)19-5-1-2-6-20(19)28(24,26)27/h1-2,5-10,17H,3-4,11-15H2
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2.60n/an/an/an/an/an/an/an/a



POSTECH

Curated by ChEMBL


Assay Description
In vitro binding affinity against 5-HT1A receptor of rat hippocampus using [3H]-8-OH-DPAT


Bioorg Med Chem Lett 9: 1379-84 (1999)


Article DOI: 10.1016/s0960-894x(99)00201-2
BindingDB Entry DOI: 10.7270/Q2862FMC
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A


(Rattus norvegicus (rat))
BDBM50077658
PNG
(1,1-Dioxo-2-[4-(3-phenyl-pyrrolidin-1-yl)-butyl]-1...)
Show SMILES O=C1N(CCCCN2CCC(C2)c2ccccc2)S(=O)(=O)c2ccccc12
Show InChI InChI=1S/C21H24N2O3S/c24-21-19-10-4-5-11-20(19)27(25,26)23(21)14-7-6-13-22-15-12-18(16-22)17-8-2-1-3-9-17/h1-5,8-11,18H,6-7,12-16H2
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2.70n/an/an/an/an/an/an/an/a



POSTECH

Curated by ChEMBL


Assay Description
In vitro binding affinity against 5-HT1A receptor of rat hippocampus using [3H]-8-OH-DPAT


Bioorg Med Chem Lett 9: 1379-84 (1999)


Article DOI: 10.1016/s0960-894x(99)00201-2
BindingDB Entry DOI: 10.7270/Q2862FMC
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM335698
PNG
((R)-3-(3-Methyl-2-oxopiperidin-3-yl)-6-(5-methylqu...)
Show SMILES Cc1cccc2ncc(cc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C21H21N3O2/c1-13-5-3-6-18-15(13)11-14(12-23-18)17-8-7-16(19(25)24-17)21(2)9-4-10-22-20(21)26/h3,5-8,11-12H,4,9-10H2,1-2H3,(H,22,26)(H,24,25)/t21-/m1/s1
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US Patent
3.30n/an/an/an/an/an/an/an/a



Pfizer Inc

US Patent


Assay Description
To measure the ability of test compounds in the present invention to bind to the human EP3 receptor, and therefore have the potential to antagonize P...


US Patent US9738626 (2017)


BindingDB Entry DOI: 10.7270/Q2CF9S7K
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50095295
PNG
(CHEMBL3589083 | US9278953, 2)
Show SMILES Cn1ncc2c(Cl)cc(cc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C15H11Cl2N3O/c1-21-10-2-3-11-9(4-10)6-19-20-15(11)5-12-13(16)7-18-8-14(12)17/h2-4,6-8H,5H2,1H3
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US Patent
3.60 -48.2n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50108471
PNG
(3-[3'-(1H-Benzoimidazol-2-ylamino)-biphenyl-3-sulf...)
Show SMILES OC(=O)CC(NS(=O)(=O)c1cccc(c1)-c1cccc(Nc2nc3ccccc3[nH]2)c1)c1ccccc1
Show InChI InChI=1S/C28H24N4O4S/c33-27(34)18-26(19-8-2-1-3-9-19)32-37(35,36)23-13-7-11-21(17-23)20-10-6-12-22(16-20)29-28-30-24-14-4-5-15-25(24)31-28/h1-17,26,32H,18H2,(H,33,34)(H2,29,30,31)
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4n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
In vitro activity in an vitronectin receptor (alpha v beta3) scintillation bead assay using 125-I labelled echistatin as a radioligand


Bioorg Med Chem Lett 12: 205-8 (2001)


Article DOI: 10.1016/s0960-894x(01)00717-x
BindingDB Entry DOI: 10.7270/Q27945T7
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125309
PNG
((S)-3-[3'-(3-Propyl-ureido)-biphenyl-4-yloxy]-2-(2...)
Show SMILES CCCNC(=O)Nc1cccc(c1)-c1ccc(OC[C@H](NS(=O)(=O)c2c(C)cc(C)cc2C)C(O)=O)cc1
Show InChI InChI=1S/C28H33N3O6S/c1-5-13-29-28(34)30-23-8-6-7-22(16-23)21-9-11-24(12-10-21)37-17-25(27(32)33)31-38(35,36)26-19(3)14-18(2)15-20(26)4/h6-12,14-16,25,31H,5,13,17H2,1-4H3,(H,32,33)(H2,29,30,34)/t25-/m0/s1
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4n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50108454
PNG
(2-{3-[3'-(2-Carboxy-1-phenyl-ethylsulfamoyl)-biphe...)
Show SMILES OC(=O)CC(NS(=O)(=O)c1cccc(c1)-c1cccc(NC(=O)Nc2[nH]c3ccccc3[nH+]2)c1)c1ccccc1
Show InChI InChI=1S/C29H25N5O5S/c35-27(36)18-26(19-8-2-1-3-9-19)34-40(38,39)23-13-7-11-21(17-23)20-10-6-12-22(16-20)30-29(37)33-28-31-24-14-4-5-15-25(24)32-28/h1-17,26,34H,18H2,(H,35,36)(H3,30,31,32,33,37)/p+1
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4n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Displacement of 125-I echistatin from Vitronectin receptor (alpha v beta3)


Bioorg Med Chem Lett 12: 205-8 (2001)


Article DOI: 10.1016/s0960-894x(01)00717-x
BindingDB Entry DOI: 10.7270/Q27945T7
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125305
PNG
((S)-3-[3'-(3-Propyl-ureido)-biphenyl-4-yl]-2-(2,4,...)
Show SMILES CCCNC(=O)Nc1cccc(c1)-c1ccc(C[C@H](NS(=O)(=O)c2c(C)cc(C)cc2C)C(O)=O)cc1
Show InChI InChI=1S/C28H33N3O5S/c1-5-13-29-28(34)30-24-8-6-7-23(17-24)22-11-9-21(10-12-22)16-25(27(32)33)31-37(35,36)26-19(3)14-18(2)15-20(26)4/h6-12,14-15,17,25,31H,5,13,16H2,1-4H3,(H,32,33)(H2,29,30,34)/t25-/m0/s1
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4n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A


(Rattus norvegicus (rat))
BDBM50077664
PNG
(2-{4-[3-(4-Fluoro-phenyl)-pyrrolidin-1-yl]-butyl}-...)
Show SMILES Fc1ccc(cc1)C1CCN(CCCCN2C(=O)c3ccccc3S2(=O)=O)C1
Show InChI InChI=1S/C21H23FN2O3S/c22-18-9-7-16(8-10-18)17-11-14-23(15-17)12-3-4-13-24-21(25)19-5-1-2-6-20(19)28(24,26)27/h1-2,5-10,17H,3-4,11-15H2
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4.20n/an/an/an/an/an/an/an/a



POSTECH

Curated by ChEMBL


Assay Description
In vitro binding affinity against 5-HT1A receptor of rat hippocampus using [3H]-8-OH-DPAT


Bioorg Med Chem Lett 9: 1379-84 (1999)


Article DOI: 10.1016/s0960-894x(99)00201-2
BindingDB Entry DOI: 10.7270/Q2862FMC
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50414549
PNG
(CHEMBL563480)
Show SMILES CCN1CCOc2ccc(cc12)C(=O)Nc1nnc(s1)-c1c(Cl)cccc1Cl
Show InChI InChI=1S/C19H16Cl2N4O2S/c1-2-25-8-9-27-15-7-6-11(10-14(15)25)17(26)22-19-24-23-18(28-19)16-12(20)4-3-5-13(16)21/h3-7,10H,2,8-9H2,1H3,(H,22,24,26)
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4.40n/an/an/an/an/an/an/an/a



Pfizer Inc

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human recombinant EP3 receptor expressed in human Chem1 cell membrane by scintillation proximity assay


Bioorg Med Chem Lett 26: 2670-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.04.009
BindingDB Entry DOI: 10.7270/Q2CJ8GDR
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM335700
PNG
((R)-6-(5-Ethylquinolin-7-yl)-3-(3-methyl-2-oxopipe...)
Show SMILES CCc1cc(cc2ncccc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C22H23N3O2/c1-3-14-12-15(13-19-16(14)6-4-10-23-19)18-8-7-17(20(26)25-18)22(2)9-5-11-24-21(22)27/h4,6-8,10,12-13H,3,5,9,11H2,1-2H3,(H,24,27)(H,25,26)/t22-/m1/s1
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4.60n/an/an/an/an/an/an/an/a



Pfizer Inc

US Patent


Assay Description
To measure the ability of test compounds in the present invention to bind to the human EP3 receptor, and therefore have the potential to antagonize P...


US Patent US9738626 (2017)


BindingDB Entry DOI: 10.7270/Q2CF9S7K
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1D


(Homo sapiens (Human))
BDBM50027065
PNG
((5'alpha)-12'-hydroxy-2'-methyl-5'-(phenylmethyl)e...)
Show SMILES CN1C[C@@H](C=C2[C@H]1Cc1c[nH]c3cccc2c13)C(=O)N[C@]1(C)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O
Show InChI InChI=1S/C33H35N5O5/c1-32(35-29(39)21-15-23-22-10-6-11-24-28(22)20(17-34-24)16-25(23)36(2)18-21)31(41)38-26(14-19-8-4-3-5-9-19)30(40)37-13-7-12-27(37)33(38,42)43-32/h3-6,8-11,15,17,21,25-27,34,42H,7,12-14,16,18H2,1-2H3,(H,35,39)/t21-,25-,26+,27+,32-,33+/m1/s1
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6n/an/an/an/an/an/an/an/a



University of South Florida

Curated by ChEMBL


Assay Description
Displacement of [3H]5-carboximidotryptamine from 5-HT1D receptor after 1.5 hrs by scintillation counting


Bioorg Med Chem 19: 5756-62 (2011)


Article DOI: 10.1016/j.bmc.2011.08.033
BindingDB Entry DOI: 10.7270/Q25X29BF
More data for this
Ligand-Target Pair
G-protein coupled receptor 119 (GPR119)


(Homo sapiens (Human))
BDBM50424575
PNG
(CHEMBL2312159)
Show SMILES Cc1c(Oc2ccc(cc2F)-n2cnnn2)ncnc1N1C2CC3CC1CC(C2)N3C(=O)OC(C)(C)C
Show InChI InChI=1S/C25H29FN8O3/c1-14-22(27-12-28-23(14)36-21-6-5-15(11-20(21)26)32-13-29-30-31-32)33-16-7-18-9-17(33)10-19(8-16)34(18)24(35)37-25(2,3)4/h5-6,11-13,16-19H,7-10H2,1-4H3
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7n/an/an/an/an/an/an/an/a



Pfizer Inc

Curated by ChEMBL


Assay Description
Binding affinity to human GPR119 in HEK293FT cell membrane by radioligand binding assay


J Med Chem 56: 301-19 (2013)


Article DOI: 10.1021/jm301626p
BindingDB Entry DOI: 10.7270/Q2BG2Q91
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM335699
PNG
((R)-3-(3-Methyl-2-oxopiperidin-3-yl)-6-(5-methylqu...)
Show SMILES Cc1cc(cc2ncccc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C21H21N3O2/c1-13-11-14(12-18-15(13)5-3-9-22-18)17-7-6-16(19(25)24-17)21(2)8-4-10-23-20(21)26/h3,5-7,9,11-12H,4,8,10H2,1-2H3,(H,23,26)(H,24,25)/t21-/m1/s1
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7.20n/an/an/an/an/an/an/an/a



Pfizer Inc

US Patent


Assay Description
To measure the ability of test compounds in the present invention to bind to the human EP3 receptor, and therefore have the potential to antagonize P...


US Patent US9738626 (2017)


BindingDB Entry DOI: 10.7270/Q2CF9S7K
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM335702
PNG
((R)-6-(5-Cyclopropylquinolin-7-yl)-3-(3-methyl-2-o...)
Show SMILES C[C@@]1(CCCNC1=O)c1ccc([nH]c1=O)-c1cc(C2CC2)c2cccnc2c1
Show InChI InChI=1S/C23H23N3O2/c1-23(9-3-11-25-22(23)28)18-7-8-19(26-21(18)27)15-12-17(14-5-6-14)16-4-2-10-24-20(16)13-15/h2,4,7-8,10,12-14H,3,5-6,9,11H2,1H3,(H,25,28)(H,26,27)/t23-/m1/s1
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7.30n/an/an/an/an/an/an/an/a



Pfizer Inc

US Patent


Assay Description
To measure the ability of test compounds in the present invention to bind to the human EP3 receptor, and therefore have the potential to antagonize P...


US Patent US9738626 (2017)


BindingDB Entry DOI: 10.7270/Q2CF9S7K
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50095294
PNG
(CHEMBL3589084 | US9278953, 7)
Show SMILES Cn1cnc2cc(cc(Cl)c12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
Show InChI InChI=1S/C17H16Cl2N4O/c1-23(2)17-12-6-10(24-3)4-5-11(12)16(21-22-17)7-13-14(18)8-20-9-15(13)19/h4-6,8-9H,7H2,1-3H3
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7.80 -46.3n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125312
PNG
((S)-3-{3'-[3-(2-Trifluoromethylsulfanyl-ethyl)-ure...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(NC(=O)NCCSC(F)(F)F)c1)C(O)=O
Show InChI InChI=1S/C28H30F3N3O5S2/c1-17-13-18(2)25(19(3)14-17)41(38,39)34-24(26(35)36)15-20-7-9-21(10-8-20)22-5-4-6-23(16-22)33-27(37)32-11-12-40-28(29,30)31/h4-10,13-14,16,24,34H,11-12,15H2,1-3H3,(H,35,36)(H2,32,33,37)/t24-/m0/s1
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8n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor EP3 subtype


(Homo sapiens (Human))
BDBM335701
PNG
((R)-6-(5-Chloroquinolin-7-yl)-3-(3-methyl-2-oxopip...)
Show SMILES C[C@@]1(CCCNC1=O)c1ccc([nH]c1=O)-c1cc(Cl)c2cccnc2c1
Show InChI InChI=1S/C20H18ClN3O2/c1-20(7-3-9-23-19(20)26)14-5-6-16(24-18(14)25)12-10-15(21)13-4-2-8-22-17(13)11-12/h2,4-6,8,10-11H,3,7,9H2,1H3,(H,23,26)(H,24,25)/t20-/m1/s1
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8.90n/an/an/an/an/an/an/an/a



Pfizer Inc

US Patent


Assay Description
To measure the ability of test compounds in the present invention to bind to the human EP3 receptor, and therefore have the potential to antagonize P...


US Patent US9738626 (2017)


BindingDB Entry DOI: 10.7270/Q2CF9S7K
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM212596
PNG
(US9278953, 3)
Show SMILES CCn1ncc2c(C)cc(cc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
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9.5 -45.8n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333259
PNG
((2S,3R,4S)-2-(8-(2-(3-chlorophenyl)hydrazinyl)-[1,...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NNc3cccc(Cl)c3)nccn12
Show InChI InChI=1S/C15H15ClN6O2S/c16-8-2-1-3-9(6-8)18-19-13-15-21-20-14(22(15)5-4-17-13)12-11(24)10(23)7-25-12/h1-6,10-12,18,23-24H,7H2,(H,17,19)/t10-,11-,12-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333246
PNG
((2S,3R,4S)-2-(8-((4-methylpiperazin-1-yl)amino)-[1...)
Show SMILES CN1CCN(CC1)Nc1nccn2c(nnc12)[C@@H]1SC[C@@H](O)[C@H]1O
Show InChI InChI=1S/C14H21N7O2S/c1-19-4-6-20(7-5-19)18-12-14-17-16-13(21(14)3-2-15-12)11-10(23)9(22)8-24-11/h2-3,9-11,22-23H,4-8H2,1H3,(H,15,18)/t9-,10-,11-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333228
PNG
((2S,3R,4S)-2-(8-((furan-3-ylmethyl)amino)-[1,2,4]t...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NCc3ccoc3)nccn12
Show InChI InChI=1S/C14H15N5O3S/c20-9-7-23-11(10(9)21)13-17-18-14-12(15-2-3-19(13)14)16-5-8-1-4-22-6-8/h1-4,6,9-11,20-21H,5,7H2,(H,15,16)/t9-,10-,11-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50166587
PNG
(CHEMBL3799530)
Show SMILES CCn1ncc2c(F)cc(cc12)C(=O)Nc1nnc(s1)C1(C)CCN(CC1)C(=O)C(C)(C)O
Show InChI InChI=1S/C22H27FN6O3S/c1-5-29-16-11-13(10-15(23)14(16)12-24-29)17(30)25-20-27-26-18(33-20)22(4)6-8-28(9-7-22)19(31)21(2,3)32/h10-12,32H,5-9H2,1-4H3,(H,25,27,30)
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10n/an/an/an/an/an/an/an/a



Pfizer Inc

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human recombinant EP3 receptor expressed in human Chem1 cell membrane by scintillation proximity assay


Bioorg Med Chem Lett 26: 2670-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.04.009
BindingDB Entry DOI: 10.7270/Q2CJ8GDR
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223896
PNG
((S)-3-[3'-(2-cyclopropylamino-3,4-dioxo-cyclobut-1...)
Show SMILES CS(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(Nc2c(NC3CC3)c(=O)c2=O)c1)C(O)=O
Show InChI InChI=1S/C23H23N3O6S/c1-33(31,32)26-18(23(29)30)11-13-5-7-14(8-6-13)15-3-2-4-17(12-15)25-20-19(21(27)22(20)28)24-16-9-10-16/h2-8,12,16,18,24-26H,9-11H2,1H3,(H,29,30)/t18-/m0/s1
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10n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333260
PNG
((2S,3R,4S)-2-(8-((3,5-dichlorobenzyl)amino)-[1,2,4...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NCc3cc(Cl)cc(Cl)c3)nccn12
Show InChI InChI=1S/C16H15Cl2N5O2S/c17-9-3-8(4-10(18)5-9)6-20-14-16-22-21-15(23(16)2-1-19-14)13-12(25)11(24)7-26-13/h1-5,11-13,24-25H,6-7H2,(H,19,20)/t11-,12-,13-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333261
PNG
((2S,3R,4S)-2-(8-((2,5-dichlorobenzyl)amino)-[1,2,4...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NCc3cc(Cl)ccc3Cl)nccn12
Show InChI InChI=1S/C16H15Cl2N5O2S/c17-9-1-2-10(18)8(5-9)6-20-14-16-22-21-15(23(16)4-3-19-14)13-12(25)11(24)7-26-13/h1-5,11-13,24-25H,6-7H2,(H,19,20)/t11-,12-,13-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333227
PNG
((2S,3R,4S)-2-(8-((pyridin-4-ylmethyl)amino)-[1,2,4...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NCc3ccncc3)nccn12
Show InChI InChI=1S/C15H16N6O2S/c22-10-8-24-12(11(10)23)14-19-20-15-13(17-5-6-21(14)15)18-7-9-1-3-16-4-2-9/h1-6,10-12,22-23H,7-8H2,(H,17,18)/t10-,11-,12-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333214
PNG
((2S,3R,4S)-2-(8-((3-(trifluoromethyl)benzyl)amino)...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(NCc3cccc(c3)C(F)(F)F)nccn12
Show InChI InChI=1S/C17H16F3N5O2S/c18-17(19,20)10-3-1-2-9(6-10)7-22-14-16-24-23-15(25(16)5-4-21-14)13-12(27)11(26)8-28-13/h1-6,11-13,26-27H,7-8H2,(H,21,22)/t11-,12-,13-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
Adenosine receptor A3


(Homo sapiens (Human))
BDBM333208
PNG
((2S,3R,4S)-2-(8-(piperidin-1-yl)-[1,2,4]triazolo[4...)
Show SMILES O[C@@H]1CS[C@H]([C@@H]1O)c1nnc2c(nccn12)N1CCCCC1
Show InChI InChI=1S/C14H19N5O2S/c20-9-8-22-11(10(9)21)12-16-17-14-13(15-4-7-19(12)14)18-5-2-1-3-6-18/h4,7,9-11,20-21H,1-3,5-6,8H2/t9-,10-,11-/m1/s1
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<10n/an/an/an/an/an/an/an/a



HANDOK INC.

US Patent


Assay Description
HEK-293 cell membrane homogenates (32 μg protein), in which A3 adenosine receptors were expressed, are incubated for 120 min at 22 C. with 0.15...


US Patent US10196396 (2019)


BindingDB Entry DOI: 10.7270/Q2DJ5HQC
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125310
PNG
((S)-3-[3'-(3-Isobutyl-ureido)-biphenyl-4-yl]-2-(2,...)
Show SMILES CC(C)CNC(=O)Nc1cccc(c1)-c1ccc(C[C@H](NS(=O)(=O)c2c(C)cc(C)cc2C)C(O)=O)cc1
Show InChI InChI=1S/C29H35N3O5S/c1-18(2)17-30-29(35)31-25-8-6-7-24(16-25)23-11-9-22(10-12-23)15-26(28(33)34)32-38(36,37)27-20(4)13-19(3)14-21(27)5/h6-14,16,18,26,32H,15,17H2,1-5H3,(H,33,34)(H2,30,31,35)/t26-/m0/s1
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10n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125298
PNG
((S)-3-[3'-(3-Cyclopropyl-ureido)-4'-methyl-bipheny...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1ccc(C)c(NC(=O)NC2CC2)c1)C(O)=O
Show InChI InChI=1S/C29H33N3O5S/c1-17-13-19(3)27(20(4)14-17)38(36,37)32-26(28(33)34)15-21-6-9-22(10-7-21)23-8-5-18(2)25(16-23)31-29(35)30-24-11-12-24/h5-10,13-14,16,24,26,32H,11-12,15H2,1-4H3,(H,33,34)(H2,30,31,35)/t26-/m0/s1
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10n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125297
PNG
((S)-3-(3'-Guanidino-biphenyl-4-yl)-2-(2,4,6-trimet...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(c1)N=C(N)N)C(O)=O
Show InChI InChI=1S/C25H28N4O4S/c1-15-11-16(2)23(17(3)12-15)34(32,33)29-22(24(30)31)13-18-7-9-19(10-8-18)20-5-4-6-21(14-20)28-25(26)27/h4-12,14,22,29H,13H2,1-3H3,(H,30,31)(H4,26,27,28)/t22-/m0/s1
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11n/an/an/an/an/an/an/an/a



Bayer AG

Curated by ChEMBL


Assay Description
Binding affinity towards vitronectin receptor (alpha V-beta3) was determined


Bioorg Med Chem Lett 13: 1071-4 (2003)


Article DOI: 10.1016/s0960-894x(03)00023-4
BindingDB Entry DOI: 10.7270/Q2S46T44
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50125297
PNG
((S)-3-(3'-Guanidino-biphenyl-4-yl)-2-(2,4,6-trimet...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(c1)N=C(N)N)C(O)=O
Show InChI InChI=1S/C25H28N4O4S/c1-15-11-16(2)23(17(3)12-15)34(32,33)29-22(24(30)31)13-18-7-9-19(10-8-18)20-5-4-6-21(14-20)28-25(26)27/h4-12,14,22,29H,13H2,1-3H3,(H,30,31)(H4,26,27,28)/t22-/m0/s1
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11n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50223887
PNG
((S)-3-(3'-{3,4-dioxo-2-[(pyridin-2-ylmethyl)-amino...)
Show SMILES Cc1cc(C)c(c(C)c1)S(=O)(=O)N[C@@H](Cc1ccc(cc1)-c1cccc(Nc2c(NCc3ccccn3)c(=O)c2=O)c1)C(O)=O
Show InChI InChI=1S/C34H32N4O6S/c1-20-15-21(2)33(22(3)16-20)45(43,44)38-28(34(41)42)17-23-10-12-24(13-11-23)25-7-6-9-26(18-25)37-30-29(31(39)32(30)40)36-19-27-8-4-5-14-35-27/h4-16,18,28,36-38H,17,19H2,1-3H3,(H,41,42)/t28-/m0/s1
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11n/an/an/an/an/an/an/an/a



Bayer HealthCare AG

Curated by ChEMBL


Assay Description
Binding affinity to integrin alphavbeta3 receptor


Bioorg Med Chem Lett 17: 6151-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.039
BindingDB Entry DOI: 10.7270/Q2KS6R8S
More data for this
Ligand-Target Pair
Adrenergic receptor alpha-2


(RAT-NEONATAL RAT-Rattus norvegicus (rat))
BDBM50077662
PNG
(2-[4-(3-Phenyl-pyrrolidin-1-yl)-butyl]-2,3-dihydro...)
Show SMILES O=C1N(CCCCN2CCC(C2)c2ccccc2)Cc2ccccc12
Show InChI InChI=1S/C22H26N2O/c25-22-21-11-5-4-10-20(21)17-24(22)14-7-6-13-23-15-12-19(16-23)18-8-2-1-3-9-18/h1-5,8-11,19H,6-7,12-17H2
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11n/an/an/an/an/an/an/an/a



POSTECH

Curated by ChEMBL


Assay Description
In vitro binding affinity against Alpha-2 adrenergic receptor of rat cerebral cortex using [3H]RX-821002


Bioorg Med Chem Lett 9: 1379-84 (1999)


Article DOI: 10.1016/s0960-894x(99)00201-2
BindingDB Entry DOI: 10.7270/Q2862FMC
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM212598
PNG
(US9278953, 4)
Show SMILES Cn1ccc2ccc(cc12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCCNC1=O
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11.2 -45.4n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM212605
PNG
(US9278953, 9)
Show SMILES Cn1ccc2cc(cc(F)c12)-c1ccc(c(=O)[nH]1)[C@@]1(C)CCNC1=O
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11.9 -45.2n/an/an/an/an/a7.425



Pfizer Inc

US Patent


Assay Description
Test compounds were half log serially diluted in 100% DMSO (J. T. Baker #922401). 1 uL of each compound was added to appropriate wells of a 384-well ...


US Patent US9278953 (2016)


BindingDB Entry DOI: 10.7270/Q2W37V5Z
More data for this
Ligand-Target Pair
Prostaglandin E2 receptor


(Homo sapiens (Human))
BDBM50166584
PNG
(CHEMBL3797819)
Show SMILES CCn1ncc2c(F)cc(cc12)C(=O)Nc1nnc(s1)C1(C)CCN(CC1)C(C)=O
Show InChI InChI=1S/C20H23FN6O2S/c1-4-27-16-10-13(9-15(21)14(16)11-22-27)17(29)23-19-25-24-18(30-19)20(3)5-7-26(8-6-20)12(2)28/h9-11H,4-8H2,1-3H3,(H,23,25,29)
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12n/an/an/an/an/an/an/an/a



Pfizer Inc

Curated by ChEMBL


Assay Description
Displacement of [3H]PGE2 from human recombinant EP3 receptor expressed in human Chem1 cell membrane by scintillation proximity assay


Bioorg Med Chem Lett 26: 2670-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.04.009
BindingDB Entry DOI: 10.7270/Q2CJ8GDR
More data for this
Ligand-Target Pair
Adrenergic receptor alpha-2


(RAT-NEONATAL RAT-Rattus norvegicus (rat))
BDBM50077660
PNG
(2-{4-[3-(4-Chloro-phenyl)-pyrrolidin-1-yl]-butyl}-...)
Show SMILES Clc1ccc(cc1)C1CCN(CCCCN2Cc3ccccc3C2=O)C1
Show InChI InChI=1S/C22H25ClN2O/c23-20-9-7-17(8-10-20)18-11-14-24(15-18)12-3-4-13-25-16-19-5-1-2-6-21(19)22(25)26/h1-2,5-10,18H,3-4,11-16H2
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12n/an/an/an/an/an/an/an/a



POSTECH

Curated by ChEMBL


Assay Description
In vitro binding affinity against Alpha-2 adrenergic receptor of rat cerebral cortex using [3H]RX-821002


Bioorg Med Chem Lett 9: 1379-84 (1999)


Article DOI: 10.1016/s0960-894x(99)00201-2
BindingDB Entry DOI: 10.7270/Q2862FMC
More data for this
Ligand-Target Pair
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