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Compile Data Set for Download or QSAR

Found 31 hits with Last Name = 'petrini? grba' and Initial = 'a'   
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
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM188286
PNG
(US9073941, 605)
Show SMILES COc1ccc(cc1)-c1nn(C)c2nc(=O)n(C)c(=O)c2n1
Show InChI InChI=1S/C14H13N5O3/c1-18-13(20)10-12(16-14(18)21)19(2)17-11(15-10)8-4-6-9(22-3)7-5-8/h4-7H,1-3H3
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n/an/a 8n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581144
PNG
(CHEMBL5087050)
Show SMILES CNC(=O)[C@H]1Cc2ccc(NC(=O)C(Cc3cc(ccc3Cl)-c3cccc(CCC(=O)N1)c3)NC(=O)c1ccnn1C)cc2 |r|
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TBA

Assay Description
Inhibition of IL-17A (unknown origin) measured by FRET assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538952
PNG
(CHEMBL4648732)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccc(cc1)C#N
Show InChI InChI=1S/C14H10N6O2/c1-19-13(21)10-12(17-14(19)22)20(2)18-11(16-10)9-5-3-8(7-15)4-6-9/h3-6H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538954
PNG
(CHEMBL4646339)
Show SMILES CN(C)c1ccccc1-c1nn(C)c2nc(=O)n(C)c(=O)c2n1
Show InChI InChI=1S/C15H16N6O2/c1-19(2)10-8-6-5-7-9(10)12-16-11-13(21(4)18-12)17-15(23)20(3)14(11)22/h5-8H,1-4H3
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n/an/a 16n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538953
PNG
(CHEMBL1316847)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccncc1
Show InChI InChI=1S/C12H10N6O2/c1-17-11(19)8-10(15-12(17)20)18(2)16-9(14-8)7-3-5-13-6-4-7/h3-6H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50438921
PNG
(CHEMBL1394266)
Show SMILES Cn1nc(Cc2ccccc2)nc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C14H13N5O2/c1-18-13(20)11-12(16-14(18)21)19(2)17-10(15-11)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538950
PNG
(CHEMBL4640696)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C13H12N6O4S/c1-18-12(20)9-11(16-13(18)21)19(2)17-10(15-9)7-3-5-8(6-4-7)24(14,22)23/h3-6H,1-2H3,(H2,14,22,23)
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM188291
PNG
(US9073941, 616)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccc(F)cc1
Show InChI InChI=1S/C13H10FN5O2/c1-18-12(20)9-11(16-13(18)21)19(2)17-10(15-9)7-3-5-8(14)6-4-7/h3-6H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581142
PNG
(CHEMBL3785600)
Show SMILES Clc1ccccc1C[C@H](NC(=O)Cc1ccccc1)C(=O)Nc1ccc(C[C@H]2NC(=O)CC3(CCCC3)CC(=O)NCCCCCNC(=O)CNC2=O)cc1 |r|
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TBA

Assay Description
Inhibition of IL-17A (unknown origin) by ELISA II


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581141
PNG
(CHEMBL5075374)
Show SMILES FC(F)(C(=O)N[C@@H](Cc1ccccc1Cl)C(=O)Nc1ccc(CCNC(=O)CC2(CC(=O)N3CCCC3)CCCC2)cc1)c1ccccc1 |r|
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TBA

Assay Description
Inhibition of IL-17A (unknown origin) by ELISA II


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM36527
PNG
(1,6-dimethyl-3-phenyl-1H,5H,6H,7H-pyrimido[5,4-e][...)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccccc1
Show InChI InChI=1S/C13H11N5O2/c1-17-12(19)9-11(15-13(17)20)18(2)16-10(14-9)8-6-4-3-5-7-8/h3-7H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581145
PNG
(CHEMBL5079201)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](N)CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CS)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CS)C(O)=O |r|
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TBA

Assay Description
Inhibition of IL-17A (unknown origin) measured by AlphaLISA assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581146
PNG
(CHEMBL5069442)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)CS)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O |r|
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TBA

Assay Description
Inhibition of IL-17A (unknown origin) measured by AlphaLISA assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538951
PNG
(CHEMBL4649004)
Show SMILES Cn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccc(O)cc1
Show InChI InChI=1S/C13H11N5O3/c1-17-12(20)9-11(15-13(17)21)18(2)16-10(14-9)7-3-5-8(19)6-4-7/h3-6,19H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM32102
PNG
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)
Show SMILES Cn1ncnc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
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n/an/a 500n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin)


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM32102
PNG
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)
Show SMILES Cn1ncnc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
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Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581143
PNG
(CHEMBL5077648)
Show SMILES CN(C)C(=O)CC1(CC(=O)NCCc2ccc(NC(=O)[C@H](Cc3ccccc3F)NC(=O)c3ccnn3C)cc2)CCCC1 |r|
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n/an/a 1.14E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of IL-17A (unknown origin) measured by FRET assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Lysine-specific demethylase 4A


(Homo sapiens (Human))
BDBM32102
PNG
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)
Show SMILES Cn1ncnc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
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n/an/a 2.50E+3n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4A (unknown origin)


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538956
PNG
(CHEMBL4646564)
Show SMILES Cn1c(=O)nc2[nH]nc(nc2c1=O)-c1ccccc1
Show InChI InChI=1S/C12H9N5O2/c1-17-11(18)8-10(14-12(17)19)16-15-9(13-8)7-5-3-2-4-6-7/h2-6H,1H3,(H,14,16,19)
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n/an/a 7.63E+3n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50581137
PNG
(CHEMBL5091151)
Show SMILES [H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]1[C@H](C)[C@@H](O[C@]2([H])O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN(C)C(=O)C[C@@H](Cc2ccc(NC(=O)[C@H](Cc3ccccc3Cl)NC(=O)Cc3ccccc3)cc2)NC(=O)[C@@H](NC(=O)[C@@H]1C)C(C)C |r|
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n/an/a>1.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human ERG by fluorescence polarization assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50581138
PNG
(CHEMBL5094466)
Show SMILES [H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]1[C@H](C)[C@@H](O[C@]2([H])O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN(C)C(=O)C[C@@H](Cc2ccc(NC(=O)[C@H](Cc3ccccc3Cl)NC(=O)Nc3ccccc3)cc2)NC(=O)[C@@H](NC(=O)[C@@H]1C)C(C)C |r|
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n/an/a 1.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human ERG by fluorescence polarization assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50581140
PNG
(CHEMBL5082420)
Show SMILES [H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]1[C@H](C)[C@@H](O[C@]2([H])O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN(C)C(=O)C[C@@H](Cc2ccc(NC(=O)[C@H](Cc3ccccc3Cl)NC(C)=O)cc2)NC(=O)[C@@H](NC(=O)[C@@H]1C)C(C)C |r|
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TBA

Assay Description
Inhibition of human ERG by fluorescence polarization assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538955
PNG
(CHEMBL4636575)
Show SMILES Cn1c(=O)[nH]c2ccc(cc2c1=O)-c1ccccc1
Show InChI InChI=1S/C15H12N2O2/c1-17-14(18)12-9-11(10-5-3-2-4-6-10)7-8-13(12)16-15(17)19/h2-9H,1H3,(H,16,19)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50581139
PNG
(CHEMBL5075025)
Show SMILES [H][C@@]1(C[C@@](C)(OC)[C@@H](O)[C@H](C)O1)O[C@H]1[C@H](C)[C@@H](O[C@]2([H])O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)CN(C)C(=O)C[C@@H](Cc2ccc(NC(=O)[C@H](Cc3ccccc3Cl)NC(=O)NCc3ccccc3)cc2)NC(=O)[C@@H](NC(=O)[C@@H]1C)C(C)C |r|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human ERG by fluorescence polarization assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Lysine-specific demethylase 4C


(Homo sapiens (Human))
BDBM50538957
PNG
(CHEMBL4640130)
Show SMILES Cn1c2nc(nn(C)c2nc1=O)-c1ccccc1
Show InChI InChI=1S/C12H11N5O/c1-16-10-11(14-12(16)18)17(2)15-9(13-10)8-6-4-3-5-7-8/h3-7H,1-2H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.27E+4n/an/an/an/an/an/a



Fidelta Ltd.

Curated by ChEMBL


Assay Description
Inhibition of KDM4C (unknown origin) using methylated H3 peptide as substrate by chemiluminescence assay


Bioorg Med Chem 28: (2020)


Article DOI: 10.1016/j.bmc.2019.115128
BindingDB Entry DOI: 10.7270/Q2251NQM
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581146
PNG
(CHEMBL5069442)
Show SMILES CSCC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)CS)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)NCC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/a 73n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581145
PNG
(CHEMBL5079201)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](N)CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CS)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CS)C(O)=O |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/a 30n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581143
PNG
(CHEMBL5077648)
Show SMILES CN(C)C(=O)CC1(CC(=O)NCCc2ccc(NC(=O)[C@H](Cc3ccccc3F)NC(=O)c3ccnn3C)cc2)CCCC1 |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
PDB
Article
PubMed
n/an/an/a<660n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Interleukin-17A


(Homo sapiens (Human))
BDBM50581142
PNG
(CHEMBL3785600)
Show SMILES Clc1ccccc1C[C@H](NC(=O)Cc1ccccc1)C(=O)Nc1ccc(C[C@H]2NC(=O)CC3(CCCC3)CC(=O)NCCCCCNC(=O)CNC2=O)cc1 |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/a<500n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581141
PNG
(CHEMBL5075374)
Show SMILES FC(F)(C(=O)N[C@@H](Cc1ccccc1Cl)C(=O)Nc1ccc(CCNC(=O)CC2(CC(=O)N3CCCC3)CCCC2)cc1)c1ccccc1 |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/a<500n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair
Interleukin-17A


(Homo sapiens (Human))
BDBM50581144
PNG
(CHEMBL5087050)
Show SMILES CNC(=O)[C@H]1Cc2ccc(NC(=O)C(Cc3cc(ccc3Cl)-c3cccc(CCC(=O)N1)c3)NC(=O)c1ccnn1C)cc2 |r|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/a<141n/an/an/an/an/a


TBA

Assay Description
Binding affinity to IL-17A (unknown origin) measured by SPR assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c00327
BindingDB Entry DOI: 10.7270/Q2639TMX
More data for this
Ligand-Target Pair