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Compile Data Set for Download or QSAR

Found 94 hits with Last Name = 'sherbukhin' and Initial = 'v'   
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
Protein M2-1


(Human respiratory syncytial virus A (strain A2))
BDBM50256886
PNG
(CHEMBL4091425)
Show SMILES Cc1cnc(N2CC3(C2)CCOCC3)c(c1)C(=O)Nc1ccc(cc1)C(=O)N1CCc2cc(sc2-c2ccccc12)-c1nc2cccc(F)c2[nH]1
Show InChI InChI=1S/C40H35FN6O3S/c1-24-19-29(37(42-21-24)46-22-40(23-46)14-17-50-18-15-40)38(48)43-27-11-9-25(10-12-27)39(49)47-16-13-26-20-33(51-35(26)28-5-2-3-8-32(28)47)36-44-31-7-4-6-30(41)34(31)45-36/h2-12,19-21H,13-18,22-23H2,1H3,(H,43,48)(H,44,45)
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n/an/a 2n/an/an/an/an/an/a



Sygnature Discovery Ltd., BioCity, Nottingham NG1 1GF, United Kingdom. Electronic address: e.fordyce@sygnaturediscovery.com.

Curated by ChEMBL


Assay Description
Inhibition of Respiratory syncytial virus A2 M2-1 by luciferase reporter-based RSV minigenome assay


Bioorg Med Chem Lett 27: 2201-2206 (2017)


Article DOI: 10.1016/j.bmcl.2017.03.053
BindingDB Entry DOI: 10.7270/Q29Z97BV
More data for this
Ligand-Target Pair
Phosphoprotein


(Human respiratory syncytial virus A (strain A2))
BDBM50256886
PNG
(CHEMBL4091425)
Show SMILES Cc1cnc(N2CC3(C2)CCOCC3)c(c1)C(=O)Nc1ccc(cc1)C(=O)N1CCc2cc(sc2-c2ccccc12)-c1nc2cccc(F)c2[nH]1
Show InChI InChI=1S/C40H35FN6O3S/c1-24-19-29(37(42-21-24)46-22-40(23-46)14-17-50-18-15-40)38(48)43-27-11-9-25(10-12-27)39(49)47-16-13-26-20-33(51-35(26)28-5-2-3-8-32(28)47)36-44-31-7-4-6-30(41)34(31)45-36/h2-12,19-21H,13-18,22-23H2,1H3,(H,43,48)(H,44,45)
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n/an/a 2n/an/an/an/an/an/a



Sygnature Discovery Ltd., BioCity, Nottingham NG1 1GF, United Kingdom. Electronic address: e.fordyce@sygnaturediscovery.com.

Curated by ChEMBL


Assay Description
Inhibition of Respiratory syncytial virus A2 protein P by luciferase reporter-based RSV minigenome assay


Bioorg Med Chem Lett 27: 2201-2206 (2017)


Article DOI: 10.1016/j.bmcl.2017.03.053
BindingDB Entry DOI: 10.7270/Q29Z97BV
More data for this
Ligand-Target Pair
Nucleoprotein


(Human respiratory syncytial virus A (strain A2))
BDBM50256886
PNG
(CHEMBL4091425)
Show SMILES Cc1cnc(N2CC3(C2)CCOCC3)c(c1)C(=O)Nc1ccc(cc1)C(=O)N1CCc2cc(sc2-c2ccccc12)-c1nc2cccc(F)c2[nH]1
Show InChI InChI=1S/C40H35FN6O3S/c1-24-19-29(37(42-21-24)46-22-40(23-46)14-17-50-18-15-40)38(48)43-27-11-9-25(10-12-27)39(49)47-16-13-26-20-33(51-35(26)28-5-2-3-8-32(28)47)36-44-31-7-4-6-30(41)34(31)45-36/h2-12,19-21H,13-18,22-23H2,1H3,(H,43,48)(H,44,45)
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n/an/a 2n/an/an/an/an/an/a



Sygnature Discovery Ltd., BioCity, Nottingham NG1 1GF, United Kingdom. Electronic address: e.fordyce@sygnaturediscovery.com.

Curated by ChEMBL


Assay Description
Inhibition of Respiratory syncytial virus A2 protein N by luciferase reporter-based RSV minigenome assay


Bioorg Med Chem Lett 27: 2201-2206 (2017)


Article DOI: 10.1016/j.bmcl.2017.03.053
BindingDB Entry DOI: 10.7270/Q29Z97BV
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412708
PNG
(AC-264613 | CHEMBL494502)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1cccc(Br)c1 |r,w:2.2|
Show InChI InChI=1S/C19H18BrN3O2/c1-12(14-8-5-9-15(20)10-14)22-23-19(25)17-16(11-21-18(17)24)13-6-3-2-4-7-13/h2-10,16-17H,11H2,1H3,(H,21,24)(H,23,25)/t16-,17-/m0/s1
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n/an/an/an/a 31.6n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412708
PNG
(AC-264613 | CHEMBL494502)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1cccc(Br)c1 |r,w:2.2|
Show InChI InChI=1S/C19H18BrN3O2/c1-12(14-8-5-9-15(20)10-14)22-23-19(25)17-16(11-21-18(17)24)13-6-3-2-4-7-13/h2-10,16-17H,11H2,1H3,(H,21,24)(H,23,25)/t16-,17-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM85517
PNG
(CAS_171436-38-7 | SL-NH2 | SLIGRL-NH2)
Show SMILES [#6]-[#6]-[#6@H](-[#6])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#6])-[#6])-[#7]-[#6](=O)-[#6@@H](-[#7])-[#6]-[#8])-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](-[#7])=O |r|
Show InChI InChI=1S/C29H56N10O7/c1-7-17(6)23(39-27(45)21(12-16(4)5)38-25(43)18(30)14-40)28(46)35-13-22(41)36-19(9-8-10-34-29(32)33)26(44)37-20(24(31)42)11-15(2)3/h15-21,23,40H,7-14,30H2,1-6H3,(H2,31,42)(H,35,46)(H,36,41)(H,37,44)(H,38,43)(H,39,45)(H4,32,33,34)/t17-,18-,19-,20-,21-,23-/m0/s1
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n/an/an/an/a 1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412709
PNG
(CHEMBL461639)
Show SMILES [#6]\[#6](-[#6])=[#6]\[#7]-1-[#6]-[#6@H](-[#6@H](-[#6](=O)-[#7]-[#7]=[#6](-[#6])-c2cccc(Br)c2)-[#6]1=O)-c1ccccc1 |r,w:11.10|
Show InChI InChI=1S/C23H24BrN3O2/c1-15(2)13-27-14-20(17-8-5-4-6-9-17)21(23(27)29)22(28)26-25-16(3)18-10-7-11-19(24)12-18/h4-13,20-21H,14H2,1-3H3,(H,26,28)/t20-,21+/m0/s1
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n/an/an/an/a 50.1n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412710
PNG
(CHEMBL459724)
Show SMILES CN(N=C(C)c1cccc(Br)c1)C(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1 |r,w:2.1|
Show InChI InChI=1S/C20H20BrN3O2/c1-13(15-9-6-10-16(21)11-15)23-24(2)20(26)18-17(12-22-19(18)25)14-7-4-3-5-8-14/h3-11,17-18H,12H2,1-2H3,(H,22,25)/t17-,18-/m0/s1
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n/an/an/an/a 6.31E+3n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412711
PNG
(CHEMBL459723)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1cccc(Br)c1)c1cccc(Br)c1 |r,w:2.2|
Show InChI InChI=1S/C19H17Br2N3O2/c1-11(12-4-2-6-14(20)8-12)23-24-19(26)17-16(10-22-18(17)25)13-5-3-7-15(21)9-13/h2-9,16-17H,10H2,1H3,(H,22,25)(H,24,26)/t16-,17-/m0/s1
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n/an/an/an/a 25.1n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412712
PNG
(CHEMBL459509)
Show SMILES Brc1ccc2CCC(=NNC(=O)[C@H]3[C@@H](CNC3=O)c3ccccc3)c2c1 |r,w:8.8|
Show InChI InChI=1S/C20H18BrN3O2/c21-14-8-6-13-7-9-17(15(13)10-14)23-24-20(26)18-16(11-22-19(18)25)12-4-2-1-3-5-12/h1-6,8,10,16,18H,7,9,11H2,(H,22,25)(H,24,26)/t16-,18-/m0/s1
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n/an/an/an/a 126n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412713
PNG
(CHEMBL493704)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1ccc(Br)s1 |r,w:2.2|
Show InChI InChI=1S/C17H16BrN3O2S/c1-10(13-7-8-14(18)24-13)20-21-17(23)15-12(9-19-16(15)22)11-5-3-2-4-6-11/h2-8,12,15H,9H2,1H3,(H,19,22)(H,21,23)/t12-,15-/m0/s1
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n/an/an/an/a 2.51E+3n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412714
PNG
(CHEMBL493494)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1ccccc1Br |r,w:2.2|
Show InChI InChI=1S/C19H18BrN3O2/c1-12(14-9-5-6-10-16(14)20)22-23-19(25)17-15(11-21-18(17)24)13-7-3-2-4-8-13/h2-10,15,17H,11H2,1H3,(H,21,24)(H,23,25)/t15-,17-/m0/s1
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n/an/an/an/a 1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412715
PNG
(CHEMBL494503)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1ccc(Br)cc1 |r,w:2.2|
Show InChI InChI=1S/C19H18BrN3O2/c1-12(13-7-9-15(20)10-8-13)22-23-19(25)17-16(11-21-18(17)24)14-5-3-2-4-6-14/h2-10,16-17H,11H2,1H3,(H,21,24)(H,23,25)/t16-,17-/m0/s1
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n/an/an/an/a 7.94E+3n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412708
PNG
(AC-264613 | CHEMBL494502)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1cccc(Br)c1 |r,w:2.2|
Show InChI InChI=1S/C19H18BrN3O2/c1-12(14-8-5-9-15(20)10-14)22-23-19(25)17-16(11-21-18(17)24)13-6-3-2-4-7-13/h2-10,16-17H,11H2,1H3,(H,21,24)(H,23,25)/t16-,17-/m0/s1
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n/an/an/an/a 31.6n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412716
PNG
(AC-98170 | CHEMBL494303)
Show SMILES CC(=NNC(=O)[C@H]1[C@@H](CNC1=O)c1ccccc1)c1cccs1 |r,w:2.2|
Show InChI InChI=1S/C17H17N3O2S/c1-11(14-8-5-9-23-14)19-20-17(22)15-13(10-18-16(15)21)12-6-3-2-4-7-12/h2-9,13,15H,10H2,1H3,(H,18,21)(H,20,22)/t13-,15-/m0/s1
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n/an/an/an/a 6.31E+3n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412717
PNG
(AC-55541 | CHEMBL493076)
Show SMILES CC(=NNC(=O)C(NC(=O)c1ccccc1)c1n[nH]c(=O)c2ccccc12)c1cccc(Br)c1 |w:2.2|
Show InChI InChI=1S/C25H20BrN5O3/c1-15(17-10-7-11-18(26)14-17)28-31-25(34)22(27-23(32)16-8-3-2-4-9-16)21-19-12-5-6-13-20(19)24(33)30-29-21/h2-14,22H,1H3,(H,27,32)(H,30,33)(H,31,34)
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n/an/an/an/a 200n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Proteinase-activated receptor 2


(Homo sapiens (Human))
BDBM50412718
PNG
(CHEMBL509819)
Show SMILES [#6]-[#6]-[#6@H](-[#6])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#6])-[#6])-[#7]-[#6](=O)-c1ccco1)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#7])-[#6](-[#7])=O |r|
Show InChI InChI=1S/C36H63N11O8/c1-7-22(6)29(47-33(52)26(18-21(4)5)46-34(53)27-13-10-16-55-27)35(54)42-19-28(48)43-24(12-9-15-41-36(39)40)31(50)45-25(17-20(2)3)32(51)44-23(30(38)49)11-8-14-37/h10,13,16,20-26,29H,7-9,11-12,14-15,17-19,37H2,1-6H3,(H2,38,49)(H,42,54)(H,43,48)(H,44,51)(H,45,50)(H,46,53)(H,47,52)(H4,39,40,41)/t22-,23-,24-,25-,26-,29-/m0/s1
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n/an/an/an/a 25.1n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Agonist activity at human PAR2 expressed in HEK293T cells assessed as effect on intracellular calcium mobilization by R-SAT assay


J Med Chem 51: 5490-3 (2008)


Article DOI: 10.1021/jm800754r
BindingDB Entry DOI: 10.7270/Q290251P
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413260
PNG
(CHEMBL198794)
Show SMILES CCCCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C22H28O2/c1-2-3-4-5-6-7-8-9-18-10-12-19(13-11-18)20-14-16-21(17-15-20)22(23)24/h10-17H,2-9H2,1H3,(H,23,24)
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n/an/an/an/a 16n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413267
PNG
(CHEMBL371684)
Show SMILES CCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C20H24O2/c1-2-3-4-5-6-7-16-8-10-17(11-9-16)18-12-14-19(15-13-18)20(21)22/h8-15H,2-7H2,1H3,(H,21,22)
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n/an/an/an/a 25n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50052414
PNG
(4-(1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthale...)
Show SMILES CC1(C)CCC(C)(C)c2cc(ccc12)C(=O)Nc1ccc(cc1)C(O)=O
Show InChI InChI=1S/C22H25NO3/c1-21(2)11-12-22(3,4)18-13-15(7-10-17(18)21)19(24)23-16-8-5-14(6-9-16)20(25)26/h5-10,13H,11-12H2,1-4H3,(H,23,24)(H,25,26)
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n/an/an/an/a 20n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413260
PNG
(CHEMBL198794)
Show SMILES CCCCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C22H28O2/c1-2-3-4-5-6-7-8-9-18-10-12-19(13-11-18)20-14-16-21(17-15-20)22(23)24/h10-17H,2-9H2,1H3,(H,23,24)
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n/an/an/an/a 316n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413272
PNG
(AC-261066 | CHEMBL198997)
Show SMILES CCCCOCCOc1nc(sc1C)-c1ccc(C(O)=O)c(F)c1
Show InChI InChI=1S/C17H20FNO4S/c1-3-4-7-22-8-9-23-15-11(2)24-16(19-15)12-5-6-13(17(20)21)14(18)10-12/h5-6,10H,3-4,7-9H2,1-2H3,(H,20,21)
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n/an/an/an/a 10n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM31883
PNG
(9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...)
Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4|
Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+
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n/an/an/an/a 25n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475526
PNG
(CHEMBL198467)
Show SMILES CCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C19H22O2/c1-2-3-4-5-6-15-7-9-16(10-8-15)17-11-13-18(14-12-17)19(20)21/h7-14H,2-6H2,1H3,(H,20,21)
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n/an/an/an/a 50n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50052414
PNG
(4-(1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthale...)
Show SMILES CC1(C)CCC(C)(C)c2cc(ccc12)C(=O)Nc1ccc(cc1)C(O)=O
Show InChI InChI=1S/C22H25NO3/c1-21(2)11-12-22(3,4)18-13-15(7-10-17(18)21)19(24)23-16-8-5-14(6-9-16)20(25)26/h5-10,13H,11-12H2,1-4H3,(H,23,24)(H,25,26)
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n/an/an/an/a 50n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM31883
PNG
(9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...)
Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4|
Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+
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n/an/an/an/a 6.30n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475527
PNG
(CHEMBL197292)
Show SMILES CCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C18H20O2/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h6-13H,2-5H2,1H3,(H,19,20)
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n/an/an/an/a 16n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413261
PNG
(AC-55649 | CHEMBL425027)
Show SMILES CCCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C21H26O2/c1-2-3-4-5-6-7-8-17-9-11-18(12-10-17)19-13-15-20(16-14-19)21(22)23/h9-16H,2-8H2,1H3,(H,22,23)
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413261
PNG
(AC-55649 | CHEMBL425027)
Show SMILES CCCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C21H26O2/c1-2-3-4-5-6-7-8-17-9-11-18(12-10-17)19-13-15-20(16-14-19)21(22)23/h9-16H,2-8H2,1H3,(H,22,23)
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n/an/an/an/a 126n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475526
PNG
(CHEMBL198467)
Show SMILES CCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C19H22O2/c1-2-3-4-5-6-15-7-9-16(10-8-15)17-11-13-18(14-12-17)19(20)21/h7-14H,2-6H2,1H3,(H,20,21)
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475527
PNG
(CHEMBL197292)
Show SMILES CCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C18H20O2/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h6-13H,2-5H2,1H3,(H,19,20)
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475528
PNG
(CHEMBL365798)
Show SMILES CCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C17H18O2/c1-2-3-4-13-5-7-14(8-6-13)15-9-11-16(12-10-15)17(18)19/h5-12H,2-4H2,1H3,(H,18,19)
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50413267
PNG
(CHEMBL371684)
Show SMILES CCCCCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C20H24O2/c1-2-3-4-5-6-7-16-8-10-17(11-9-16)18-12-14-19(15-13-18)20(21)22/h8-15H,2-7H2,1H3,(H,21,22)
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n/an/an/an/a>1.00E+4n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta1


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Retinoic acid receptor beta


(Homo sapiens (Human))
BDBM50475528
PNG
(CHEMBL365798)
Show SMILES CCCCc1ccc(cc1)-c1ccc(cc1)C(O)=O
Show InChI InChI=1S/C17H18O2/c1-2-3-4-13-5-7-14(8-6-13)15-9-11-16(12-10-15)17(18)19/h5-12H,2-4H2,1H3,(H,18,19)
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n/an/an/an/a 63n/an/an/an/a



ACADIA Pharmaceuticals AB

Curated by ChEMBL


Assay Description
Transcriptional activity against RARbeta2


J Med Chem 48: 7517-9 (2005)


Article DOI: 10.1021/jm050891r
BindingDB Entry DOI: 10.7270/Q26M39JQ
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475708
PNG
(CHEMBL425592)
Show SMILES CN(C)CCC(NC(=O)Nc1ccc(cc1)C(F)(F)F)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H21ClF3N3O/c1-26(2)12-11-17(13-3-7-15(20)8-4-13)25-18(27)24-16-9-5-14(6-10-16)19(21,22)23/h3-10,17H,11-12H2,1-2H3,(H2,24,25,27)
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n/an/an/an/a 117n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50414759
PNG
(CHEMBL574304)
Show SMILES CO[C@@H](C(=O)N[C@@H](CCN(C)C)c1ccc(Cl)cc1)c1ccccc1 |r|
Show InChI InChI=1S/C20H25ClN2O2/c1-23(2)14-13-18(15-9-11-17(21)12-10-15)22-20(24)19(25-3)16-7-5-4-6-8-16/h4-12,18-19H,13-14H2,1-3H3,(H,22,24)/t18-,19+/m0/s1
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n/an/an/an/a 871n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475709
PNG
(CHEMBL377938)
Show SMILES CN(C)CCC(NS(=O)(=O)c1ccc(C)cc1)c1ccc(Cl)cc1
Show InChI InChI=1S/C18H23ClN2O2S/c1-14-4-10-17(11-5-14)24(22,23)20-18(12-13-21(2)3)15-6-8-16(19)9-7-15/h4-11,18,20H,12-13H2,1-3H3
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n/an/an/an/a 6.46E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475710
PNG
(CHEMBL205681)
Show SMILES CN(C)CCC(NC(=O)Nc1ccc(cc1)C(C)(C)C)c1ccc(Cl)cc1
Show InChI InChI=1S/C22H30ClN3O/c1-22(2,3)17-8-12-19(13-9-17)24-21(27)25-20(14-15-26(4)5)16-6-10-18(23)11-7-16/h6-13,20H,14-15H2,1-5H3,(H2,24,25,27)
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n/an/an/an/a 275n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50164424
PNG
(3-(4-Chloro-phenyl)-3-(2-dimethylamino-ethyl)-isoc...)
Show SMILES CN(C)CCC1(Cc2ccccc2C(=O)O1)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H20ClNO2/c1-21(2)12-11-19(15-7-9-16(20)10-8-15)13-14-5-3-4-6-17(14)18(22)23-19/h3-10H,11-13H2,1-2H3
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n/an/an/an/a 1.12E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475711
PNG
(CHEMBL203337)
Show SMILES CN(C)CCC(NC(=O)c1ccccc1)c1ccc(Cl)cc1
Show InChI InChI=1S/C18H21ClN2O/c1-21(2)13-12-17(14-8-10-16(19)11-9-14)20-18(22)15-6-4-3-5-7-15/h3-11,17H,12-13H2,1-2H3,(H,20,22)
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n/an/an/an/a 1.41E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475712
PNG
(CHEMBL382477)
Show SMILES CN(C)CCC(NC(=O)NCc1ccccc1)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H24ClN3O/c1-23(2)13-12-18(16-8-10-17(20)11-9-16)22-19(24)21-14-15-6-4-3-5-7-15/h3-11,18H,12-14H2,1-2H3,(H2,21,22,24)
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n/an/an/an/a 2.00E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475713
PNG
(CHEMBL206661)
Show SMILES CN(C)CCC(OC(=O)c1ccc2ccccc2c1)c1ccc(Cl)cc1
Show InChI InChI=1S/C22H22ClNO2/c1-24(2)14-13-21(17-9-11-20(23)12-10-17)26-22(25)19-8-7-16-5-3-4-6-18(16)15-19/h3-12,15,21H,13-14H2,1-2H3
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n/an/an/an/a 2.09E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475714
PNG
(CHEMBL208536)
Show SMILES COc1cccc(NC(=O)OC(CCN(C)C)c2ccc(Cl)cc2)c1
Show InChI InChI=1S/C19H23ClN2O3/c1-22(2)12-11-18(14-7-9-15(20)10-8-14)25-19(23)21-16-5-4-6-17(13-16)24-3/h4-10,13,18H,11-12H2,1-3H3,(H,21,23)
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n/an/an/an/a 1.12E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475715
PNG
(CHEMBL203051)
Show SMILES CN(C)CCC(OC(=O)Nc1ccc(cc1)C(F)(F)F)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H20ClF3N2O2/c1-25(2)12-11-17(13-3-7-15(20)8-4-13)27-18(26)24-16-9-5-14(6-10-16)19(21,22)23/h3-10,17H,11-12H2,1-2H3,(H,24,26)
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n/an/an/an/a 251n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475716
PNG
(CHEMBL205157)
Show SMILES CCc1ccccc1C(=O)N[C@@H](CCN(C)C)c1ccc(Cl)cc1
Show InChI InChI=1S/C20H25ClN2O/c1-4-15-7-5-6-8-18(15)20(24)22-19(13-14-23(2)3)16-9-11-17(21)12-10-16/h5-12,19H,4,13-14H2,1-3H3,(H,22,24)/t19-/m0/s1
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n/an/an/an/a 1.02E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475717
PNG
(CHEMBL208436)
Show SMILES CN(C)CCC(OC(=O)c1ccc(Br)cc1C)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H21BrClNO2/c1-13-12-15(20)6-9-17(13)19(23)24-18(10-11-22(2)3)14-4-7-16(21)8-5-14/h4-9,12,18H,10-11H2,1-3H3
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n/an/an/an/a 1.07E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475718
PNG
(CHEMBL208886)
Show SMILES COc1ccc(cc1)C(=O)OC(CCN(C)C)c1ccc(Cl)cc1
Show InChI InChI=1S/C19H22ClNO3/c1-21(2)13-12-18(14-4-8-16(20)9-5-14)24-19(22)15-6-10-17(23-3)11-7-15/h4-11,18H,12-13H2,1-3H3
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n/an/an/an/a 2.19E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475719
PNG
(CHEMBL205735)
Show SMILES COc1ccc(NC(=O)NC(CCN(C)C)c2ccc(Cl)cc2)cc1
Show InChI InChI=1S/C19H24ClN3O2/c1-23(2)13-12-18(14-4-6-15(20)7-5-14)22-19(24)21-16-8-10-17(25-3)11-9-16/h4-11,18H,12-13H2,1-3H3,(H2,21,22,24)
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n/an/an/an/a 2.00E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475720
PNG
(CHEMBL206719)
Show SMILES CN(C)CCC(OC(=O)c1cccc2ccccc12)c1ccc(Cl)cc1
Show InChI InChI=1S/C22H22ClNO2/c1-24(2)15-14-21(17-10-12-18(23)13-11-17)26-22(25)20-9-5-7-16-6-3-4-8-19(16)20/h3-13,21H,14-15H2,1-2H3
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n/an/an/an/a 2.29E+3n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
Urotensin-2 receptor


(Homo sapiens (Human))
BDBM50475721
PNG
(CHEMBL206551)
Show SMILES CN(C)CCC(NC(=O)Nc1ccc2ccccc2c1)c1ccc(Cl)cc1
Show InChI InChI=1S/C22H24ClN3O/c1-26(2)14-13-21(17-7-10-19(23)11-8-17)25-22(27)24-20-12-9-16-5-3-4-6-18(16)15-20/h3-12,15,21H,13-14H2,1-2H3,(H2,24,25,27)
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n/an/an/an/a 288n/an/an/an/a



G£teborg University

Curated by ChEMBL


Assay Description
Activity against human urotensin-2 receptor expressed in NIH3T3 cells


J Med Chem 49: 2232-40 (2006)


Article DOI: 10.1021/jm051121i
BindingDB Entry DOI: 10.7270/Q24Q7XQB
More data for this
Ligand-Target Pair
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