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Compile Data Set for Download or QSAR

Found 70 hits with Last Name = 'sumiyoshi' and Initial = 't'   
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
cAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D


(Homo sapiens (Human))
BDBM50497250
PNG
(CHEMBL3299084)
Show SMILES Oc1cnccc1CCCOc1cccnc1Oc1cccc(Cl)c1
Show InChI InChI=1S/C19H17ClN2O3/c20-15-5-1-6-16(12-15)25-19-18(7-2-9-22-19)24-11-3-4-14-8-10-21-13-17(14)23/h1-2,5-10,12-13,23H,3-4,11H2
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n/an/a 33n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human PDE4


Bioorg Med Chem Lett 24: 2689-92 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.052
BindingDB Entry DOI: 10.7270/Q2XD14P4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594395
PNG
(CHEMBL5189146)
Show SMILES ONC(=O)c1ccc(CN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 110n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044633
PNG
(CHEMBL3310801)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CN(C(N)=O)c4ncccc34)CC2)CC1
Show InChI InChI=1S/C21H31N5O3/c1-2-29-20(28)25-10-5-16(6-11-25)14-24-12-7-21(8-13-24)15-26(19(22)27)18-17(21)4-3-9-23-18/h3-4,9,16H,2,5-8,10-15H2,1H3,(H2,22,27)
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n/an/a 190n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044630
PNG
(CHEMBL3310798)
Show SMILES CCNC(=O)N1CC2(CCN(CC3CCN(CC3)C(=O)OCC)CC2)c2cccnc12
Show InChI InChI=1S/C23H35N5O3/c1-3-24-21(29)28-17-23(19-6-5-11-25-20(19)28)9-14-26(15-10-23)16-18-7-12-27(13-8-18)22(30)31-4-2/h5-6,11,18H,3-4,7-10,12-17H2,1-2H3,(H,24,29)
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n/an/a 230n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594401
PNG
(CHEMBL5192796)
Show SMILES ONC(=O)c1ccc(CN2CCN(Cc3ccccc3)CC2)cc1
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n/an/a 260n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594394
PNG
(CHEMBL5195750)
Show SMILES CC(N1CCN(Cc2ccc(cc2)C(=O)NO)CC1)c1ccccc1
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n/an/a 260n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044632
PNG
(CHEMBL3310800)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CN(C(=O)NC)c4ncccc34)CC2)CC1
Show InChI InChI=1S/C22H33N5O3/c1-3-30-21(29)26-11-6-17(7-12-26)15-25-13-8-22(9-14-25)16-27(20(28)23-2)19-18(22)5-4-10-24-19/h4-5,10,17H,3,6-9,11-16H2,1-2H3,(H,23,28)
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n/an/a 300n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594396
PNG
(CHEMBL5172611)
Show SMILES ONC(=O)c1ccc(CCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 330n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594398
PNG
(CHEMBL5175813)
Show SMILES ONC(=O)c1ccc(CCCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 430n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594397
PNG
(CHEMBL5193136)
Show SMILES ONC(=O)c1ccc(CCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 580n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50594395
PNG
(CHEMBL5189146)
Show SMILES ONC(=O)c1ccc(CN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50492651
PNG
(CHEMBL2407175)
Show SMILES CCCN1C(=O)CC2(CCN(CC3CCN(CC3)C(=O)OCC)CC2)c2cccnc12
Show InChI InChI=1S/C24H36N4O3/c1-3-12-28-21(29)17-24(20-6-5-11-25-22(20)28)9-15-26(16-10-24)18-19-7-13-27(14-8-19)23(30)31-4-2/h5-6,11,19H,3-4,7-10,12-18H2,1-2H3
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n/an/a 670n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50428141
PNG
(CHEMBL2336055)
Show SMILES CCOC(=O)N1CCC(CN2CC[C@@H](C2)N2C(=O)Cc3ccccc23)CC1 |r|
Show InChI InChI=1S/C21H29N3O3/c1-2-27-21(26)23-11-7-16(8-12-23)14-22-10-9-18(15-22)24-19-6-4-3-5-17(19)13-20(24)25/h3-6,16,18H,2,7-15H2,1H3/t18-/m0/s1
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n/an/a 800n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp technique


ACS Med Chem Lett 4: 244-8 (2013)


Article DOI: 10.1021/ml300372f
BindingDB Entry DOI: 10.7270/Q20Z74N3
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50492655
PNG
(CHEMBL2407171)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)OC(=O)Nc2ncccc32)CC1
Show InChI InChI=1S/C20H28N4O4/c1-2-27-19(26)24-10-5-15(6-11-24)14-23-12-7-20(8-13-23)16-4-3-9-21-17(16)22-18(25)28-20/h3-4,9,15H,2,5-8,10-14H2,1H3,(H,21,22,25)
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n/an/a 920n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50492654
PNG
(CHEMBL2407170)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)OC(=O)N(C)c2ncccc32)CC1
Show InChI InChI=1S/C21H30N4O4/c1-3-28-20(27)25-11-6-16(7-12-25)15-24-13-8-21(9-14-24)17-5-4-10-22-18(17)23(2)19(26)29-21/h4-5,10,16H,3,6-9,11-15H2,1-2H3
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n/an/a 1.48E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50459720
PNG
(CHEMBL4210305)
Show SMILES COc1ccc(CN(CCN(C)C)c2ccc(cn2)C(=O)Nc2ccccc2N)cc1
Show InChI InChI=1S/C24H29N5O2/c1-28(2)14-15-29(17-18-8-11-20(31-3)12-9-18)23-13-10-19(16-26-23)24(30)27-22-7-5-4-6-21(22)25/h4-13,16H,14-15,17,25H2,1-3H3,(H,27,30)
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n/an/a 1.50E+3n/an/an/an/an/an/a



Kansai University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human C-terminal FLAG/His-tagged HDAC1 expressed in baculovirus infected Sf9 insect cells using HDAC substrate 3 measured a...


ACS Med Chem Lett 9: 884-888 (2018)


Article DOI: 10.1021/acsmedchemlett.8b00099
BindingDB Entry DOI: 10.7270/Q2JH3PTX
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50019335
PNG
(CHEMBL3289440)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CN(c4ncccc34)S(C)(=O)=O)CC2)CC1
Show InChI InChI=1S/C21H32N4O4S/c1-3-29-20(26)24-11-6-17(7-12-24)15-23-13-8-21(9-14-23)16-25(30(2,27)28)19-18(21)5-4-10-22-19/h4-5,10,17H,3,6-9,11-16H2,1-2H3
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n/an/a 1.90E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50019335
PNG
(CHEMBL3289440)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CN(c4ncccc34)S(C)(=O)=O)CC2)CC1
Show InChI InChI=1S/C21H32N4O4S/c1-3-29-20(26)24-11-6-17(7-12-24)15-23-13-8-21(9-14-23)16-25(30(2,27)28)19-18(21)5-4-10-22-19/h4-5,10,17H,3,6-9,11-16H2,1-2H3
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n/an/a 1.90E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG tail current after 5 mins by patch-clamp method


Bioorg Med Chem Lett 24: 2909-12 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.083
BindingDB Entry DOI: 10.7270/Q2BG2QKM
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594397
PNG
(CHEMBL5193136)
Show SMILES ONC(=O)c1ccc(CCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50130927
PNG
(CHEMBL3633184)
Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](CN3CC[C@H](C3)N3Cc4ccccc4NC3=O)C1)N2C(=O)OCC |r|
Show InChI InChI=1S/C23H32N4O3/c1-2-30-23(29)27-18-7-8-19(27)12-16(11-18)13-25-10-9-20(15-25)26-14-17-5-3-4-6-21(17)24-22(26)28/h3-6,16,18-20H,2,7-15H2,1H3,(H,24,28)/t16-,18-,19+,20-/m1/s1
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n/an/a>2.00E+3n/an/an/an/an/an/a



Sumitomo Dainippon Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 (unknown origin)


Bioorg Med Chem Lett 25: 5357-61 (2015)


Article DOI: 10.1016/j.bmcl.2015.09.032
BindingDB Entry DOI: 10.7270/Q2VT1TX2
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50130927
PNG
(CHEMBL3633184)
Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](CN3CC[C@H](C3)N3Cc4ccccc4NC3=O)C1)N2C(=O)OCC |r|
Show InChI InChI=1S/C23H32N4O3/c1-2-30-23(29)27-18-7-8-19(27)12-16(11-18)13-25-10-9-20(15-25)26-14-17-5-3-4-6-21(17)24-22(26)28/h3-6,16,18-20H,2,7-15H2,1H3,(H,24,28)/t16-,18-,19+,20-/m1/s1
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Sumitomo Dainippon Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 (unknown origin)


Bioorg Med Chem Lett 25: 5357-61 (2015)


Article DOI: 10.1016/j.bmcl.2015.09.032
BindingDB Entry DOI: 10.7270/Q2VT1TX2
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50130927
PNG
(CHEMBL3633184)
Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](CN3CC[C@H](C3)N3Cc4ccccc4NC3=O)C1)N2C(=O)OCC |r|
Show InChI InChI=1S/C23H32N4O3/c1-2-30-23(29)27-18-7-8-19(27)12-16(11-18)13-25-10-9-20(15-25)26-14-17-5-3-4-6-21(17)24-22(26)28/h3-6,16,18-20H,2,7-15H2,1H3,(H,24,28)/t16-,18-,19+,20-/m1/s1
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n/an/a>2.00E+3n/an/an/an/an/an/a



Sumitomo Dainippon Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 (unknown origin)


Bioorg Med Chem Lett 25: 5357-61 (2015)


Article DOI: 10.1016/j.bmcl.2015.09.032
BindingDB Entry DOI: 10.7270/Q2VT1TX2
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50130927
PNG
(CHEMBL3633184)
Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](CN3CC[C@H](C3)N3Cc4ccccc4NC3=O)C1)N2C(=O)OCC |r|
Show InChI InChI=1S/C23H32N4O3/c1-2-30-23(29)27-18-7-8-19(27)12-16(11-18)13-25-10-9-20(15-25)26-14-17-5-3-4-6-21(17)24-22(26)28/h3-6,16,18-20H,2,7-15H2,1H3,(H,24,28)/t16-,18-,19+,20-/m1/s1
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Sumitomo Dainippon Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 (unknown origin)


Bioorg Med Chem Lett 25: 5357-61 (2015)


Article DOI: 10.1016/j.bmcl.2015.09.032
BindingDB Entry DOI: 10.7270/Q2VT1TX2
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50130927
PNG
(CHEMBL3633184)
Show SMILES [H][C@]12CC[C@]([H])(C[C@@H](CN3CC[C@H](C3)N3Cc4ccccc4NC3=O)C1)N2C(=O)OCC |r|
Show InChI InChI=1S/C23H32N4O3/c1-2-30-23(29)27-18-7-8-19(27)12-16(11-18)13-25-10-9-20(15-25)26-14-17-5-3-4-6-21(17)24-22(26)28/h3-6,16,18-20H,2,7-15H2,1H3,(H,24,28)/t16-,18-,19+,20-/m1/s1
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n/an/a>2.00E+3n/an/an/an/an/an/a



Sumitomo Dainippon Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin)


Bioorg Med Chem Lett 25: 5357-61 (2015)


Article DOI: 10.1016/j.bmcl.2015.09.032
BindingDB Entry DOI: 10.7270/Q2VT1TX2
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50428138
PNG
(CHEMBL2336059)
Show SMILES CCOC(=O)N1[C@H]2CC[C@@H]1C[C@@H](CN1CC[C@@H](C1)N1C(=O)Cc3ccccc13)C2 |r,THB:3:5:11.28.10:7.8|
Show InChI InChI=1S/C23H31N3O3/c1-2-29-23(28)25-18-7-8-19(25)12-16(11-18)14-24-10-9-20(15-24)26-21-6-4-3-5-17(21)13-22(26)27/h3-6,16,18-20H,2,7-15H2,1H3/t16-,18-,19+,20-/m0/s1
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n/an/a 2.40E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp technique


ACS Med Chem Lett 4: 244-8 (2013)


Article DOI: 10.1021/ml300372f
BindingDB Entry DOI: 10.7270/Q20Z74N3
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50492653
PNG
(CHEMBL2407173)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)CC(=O)N(C)c2ncccc32)CC1
Show InChI InChI=1S/C22H32N4O3/c1-3-29-21(28)26-11-6-17(7-12-26)16-25-13-8-22(9-14-25)15-19(27)24(2)20-18(22)5-4-10-23-20/h4-5,10,17H,3,6-9,11-16H2,1-2H3
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n/an/a 2.54E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044631
PNG
(CHEMBL3310799)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CN(C(=O)N(CC)CC)c4ncccc34)CC2)CC1
Show InChI InChI=1S/C25H39N5O3/c1-4-28(5-2)23(31)30-19-25(21-8-7-13-26-22(21)30)11-16-27(17-12-25)18-20-9-14-29(15-10-20)24(32)33-6-3/h7-8,13,20H,4-6,9-12,14-19H2,1-3H3
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n/an/a 2.54E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50019334
PNG
(CHEMBL3289444)
Show SMILES CC(C)OC(=O)N1CCC(C)(CN2CCC3(CN(c4ncccc34)S(C)(=O)=O)CC2)CC1
Show InChI InChI=1S/C23H36N4O4S/c1-18(2)31-21(28)26-14-7-22(3,8-15-26)16-25-12-9-23(10-13-25)17-27(32(4,29)30)20-19(23)6-5-11-24-20/h5-6,11,18H,7-10,12-17H2,1-4H3
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n/an/a 2.75E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG tail current after 5 mins by patch-clamp method


Bioorg Med Chem Lett 24: 2909-12 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.083
BindingDB Entry DOI: 10.7270/Q2BG2QKM
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50492652
PNG
(CHEMBL2407172)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)CC(=O)Nc2ncccc32)CC1
Show InChI InChI=1S/C21H30N4O3/c1-2-28-20(27)25-10-5-16(6-11-25)15-24-12-7-21(8-13-24)14-18(26)23-19-17(21)4-3-9-22-19/h3-4,9,16H,2,5-8,10-15H2,1H3,(H,22,23,26)
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n/an/a 2.80E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044629
PNG
(CHEMBL2407174)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)CC(=O)N(CC)c2ncccc32)CC1
Show InChI InChI=1S/C23H34N4O3/c1-3-27-20(28)16-23(19-6-5-11-24-21(19)27)9-14-25(15-10-23)17-18-7-12-26(13-8-18)22(29)30-4-2/h5-6,11,18H,3-4,7-10,12-17H2,1-2H3
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n/an/a 2.89E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG by automated planar patch-clamp system


Bioorg Med Chem Lett 23: 4644-7 (2013)


Article DOI: 10.1016/j.bmcl.2013.06.013
BindingDB Entry DOI: 10.7270/Q2TQ64GH
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044629
PNG
(CHEMBL2407174)
Show SMILES CCOC(=O)N1CCC(CN2CCC3(CC2)CC(=O)N(CC)c2ncccc32)CC1
Show InChI InChI=1S/C23H34N4O3/c1-3-27-20(28)16-23(19-6-5-11-24-21(19)27)9-14-25(15-10-23)17-18-7-12-26(13-8-18)22(29)30-4-2/h5-6,11,18H,3-4,7-10,12-17H2,1-2H3
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n/an/a 2.89E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594396
PNG
(CHEMBL5172611)
Show SMILES ONC(=O)c1ccc(CCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 3.00E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50428140
PNG
(CHEMBL2336056)
Show SMILES CCOC(=O)N1CCC(C)(CN2CC[C@@H](C2)N2C(=O)Cc3ccccc23)CC1 |r|
Show InChI InChI=1S/C22H31N3O3/c1-3-28-21(27)24-12-9-22(2,10-13-24)16-23-11-8-18(15-23)25-19-7-5-4-6-17(19)14-20(25)26/h4-7,18H,3,8-16H2,1-2H3/t18-/m0/s1
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n/an/a 3.50E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp technique


ACS Med Chem Lett 4: 244-8 (2013)


Article DOI: 10.1021/ml300372f
BindingDB Entry DOI: 10.7270/Q20Z74N3
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50019336
PNG
(CHEMBL3289442)
Show SMILES CCOC(=O)N1CCC(C)(CN2CCC3(CN(c4ncccc34)S(C)(=O)=O)CC2)CC1
Show InChI InChI=1S/C22H34N4O4S/c1-4-30-20(27)25-14-7-21(2,8-15-25)16-24-12-9-22(10-13-24)17-26(31(3,28)29)19-18(22)6-5-11-23-19/h5-6,11H,4,7-10,12-17H2,1-3H3
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n/an/a 3.63E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG tail current after 5 mins by patch-clamp method


Bioorg Med Chem Lett 24: 2909-12 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.083
BindingDB Entry DOI: 10.7270/Q2BG2QKM
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594397
PNG
(CHEMBL5193136)
Show SMILES ONC(=O)c1ccc(CCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 3.80E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50428139
PNG
(CHEMBL2336057)
Show SMILES CCOC(=O)N1CCC(O)(CN2CC[C@@H](C2)N2C(=O)Cc3ccccc23)CC1 |r|
Show InChI InChI=1S/C21H29N3O4/c1-2-28-20(26)23-11-8-21(27,9-12-23)15-22-10-7-17(14-22)24-18-6-4-3-5-16(18)13-19(24)25/h3-6,17,27H,2,7-15H2,1H3/t17-/m0/s1
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n/an/a 3.90E+3n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co. Ltd.

Curated by ChEMBL


Assay Description
Inhibition of human ERG assessed as decrease in tail current amplitude measured after 5 mins by whole cell patch clamp technique


ACS Med Chem Lett 4: 244-8 (2013)


Article DOI: 10.1021/ml300372f
BindingDB Entry DOI: 10.7270/Q20Z74N3
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594395
PNG
(CHEMBL5189146)
Show SMILES ONC(=O)c1ccc(CN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 4.40E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594395
PNG
(CHEMBL5189146)
Show SMILES ONC(=O)c1ccc(CN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 4.40E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594396
PNG
(CHEMBL5172611)
Show SMILES ONC(=O)c1ccc(CCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 4.80E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594398
PNG
(CHEMBL5175813)
Show SMILES ONC(=O)c1ccc(CCCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 5.00E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594398
PNG
(CHEMBL5175813)
Show SMILES ONC(=O)c1ccc(CCCCN2CCN(CC2)C(c2ccccc2)c2ccccc2)cc1
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n/an/a 5.50E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50459720
PNG
(CHEMBL4210305)
Show SMILES COc1ccc(CN(CCN(C)C)c2ccc(cn2)C(=O)Nc2ccccc2N)cc1
Show InChI InChI=1S/C24H29N5O2/c1-28(2)14-15-29(17-18-8-11-20(31-3)12-9-18)23-13-10-19(16-26-23)24(30)27-22-7-5-4-6-21(22)25/h4-13,16H,14-15,17,25H2,1-3H3,(H,27,30)
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n/an/a 5.50E+3n/an/an/an/an/an/a



Kansai University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human C-terminal FLAG-tagged HDAC2 expressed in baculovirus infected Sf9 insect cells using HDAC substrate 3 measured after...


ACS Med Chem Lett 9: 884-888 (2018)


Article DOI: 10.1021/acsmedchemlett.8b00099
BindingDB Entry DOI: 10.7270/Q2JH3PTX
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Mus musculus)
BDBM50594400
PNG
(CHEMBL5205202)
Show SMILES ONC(=O)c1cccc(CN2CCN(CC2)C(c2ccccc2)c2ccccc2)c1
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n/an/a 6.60E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594394
PNG
(CHEMBL5195750)
Show SMILES CC(N1CCN(Cc2ccc(cc2)C(=O)NO)CC1)c1ccccc1
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n/an/a 6.70E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594401
PNG
(CHEMBL5192796)
Show SMILES ONC(=O)c1ccc(CN2CCN(Cc3ccccc3)CC2)cc1
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n/an/a 9.20E+3n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50044634
PNG
(CHEMBL3310802)
Show SMILES OC(=O)\C=C\C(O)=O.CCOC(=O)N1CCC(CN2CCC3(CN(C(=O)N(C)C)c4ncccc34)CC2)CC1
Show InChI InChI=1S/C23H35N5O3/c1-4-31-22(30)27-12-7-18(8-13-27)16-26-14-9-23(10-15-26)17-28(21(29)25(2)3)20-19(23)6-5-11-24-20/h5-6,11,18H,4,7-10,12-17H2,1-3H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Dainippon Sumitomo Pharma Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human ERG channel


Bioorg Med Chem Lett 24: 3189-93 (2014)


Article DOI: 10.1016/j.bmcl.2014.04.085
BindingDB Entry DOI: 10.7270/Q2J38V74
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50594401
PNG
(CHEMBL5192796)
Show SMILES ONC(=O)c1ccc(CN2CCN(Cc3ccccc3)CC2)cc1
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n/an/a 1.04E+4n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)


(Homo sapiens (Human))
BDBM50459720
PNG
(CHEMBL4210305)
Show SMILES COc1ccc(CN(CCN(C)C)c2ccc(cn2)C(=O)Nc2ccccc2N)cc1
Show InChI InChI=1S/C24H29N5O2/c1-28(2)14-15-29(17-18-8-11-20(31-3)12-9-18)23-13-10-19(16-26-23)24(30)27-22-7-5-4-6-21(22)25/h4-13,16H,14-15,17,25H2,1-3H3,(H,27,30)
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n/an/a 1.20E+4n/an/an/an/an/an/a



Kansai University

Curated by ChEMBL


Assay Description
Inhibition of human full length C-terminal His-tagged HDAC3/N-terminal GST-tagged human NCOR2 (395 to 489 residues) co-expressed in baculovirus infec...


ACS Med Chem Lett 9: 884-888 (2018)


Article DOI: 10.1021/acsmedchemlett.8b00099
BindingDB Entry DOI: 10.7270/Q2JH3PTX
More data for this
Ligand-Target Pair
Histone deacetylase 4


(Homo sapiens (Human))
BDBM50594394
PNG
(CHEMBL5195750)
Show SMILES CC(N1CCN(Cc2ccc(cc2)C(=O)NO)CC1)c1ccccc1
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n/an/a 1.23E+4n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acsmedchemlett.2c00081
BindingDB Entry DOI: 10.7270/Q2NG4VP5
More data for this
Ligand-Target Pair
Polyamine deacetylase HDAC10


(Homo sapiens (Human))
BDBM50459720
PNG
(CHEMBL4210305)
Show SMILES COc1ccc(CN(CCN(C)C)c2ccc(cn2)C(=O)Nc2ccccc2N)cc1
Show InChI InChI=1S/C24H29N5O2/c1-28(2)14-15-29(17-18-8-11-20(31-3)12-9-18)23-13-10-19(16-26-23)24(30)27-22-7-5-4-6-21(22)25/h4-13,16H,14-15,17,25H2,1-3H3,(H,27,30)
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n/an/a 1.55E+4n/an/an/an/an/an/a



Kansai University

Curated by ChEMBL


Assay Description
Inhibition of human HDAC10 expressed in baculovirus infected Sf9 insect cells using HDAC substrate 3 measured after 30 mins by fluorescence assay


ACS Med Chem Lett 9: 884-888 (2018)


Article DOI: 10.1021/acsmedchemlett.8b00099
BindingDB Entry DOI: 10.7270/Q2JH3PTX
More data for this
Ligand-Target Pair
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