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PubMed code 20934332

Compile data set for download or QSAR
Found 3 hits of Enzyme Inhibition Constant Data   
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
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50330096
PNG
(CHEMBL1271606 | N-((1S)-1-(3-fluorophenyl)-3-((1R,...)
Show SMILES Cc1nc2ccccc2n1C1C[C@@H]2CC[C@H](C1)N2CC[C@H](NC(=O)C1CCSCC1)c1cccc(F)c1 |r,THB:18:17:10.11.16:13.14|
Show InChI InChI=1S/C30H37FN4OS/c1-20-32-28-7-2-3-8-29(28)35(20)26-18-24-9-10-25(19-26)34(24)14-11-27(22-5-4-6-23(31)17-22)33-30(36)21-12-15-37-16-13-21/h2-8,17,21,24-27H,9-16,18-19H2,1H3,(H,33,36)/t24-,25+,26?,27-/m0/s1
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Article
PubMed
n/an/a 740n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of human ERG


Bioorg Med Chem Lett 20: 6400-4 (2010)


Article DOI: 10.1016/j.bmcl.2010.09.089
BindingDB Entry DOI: 10.7270/Q23N23M5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50330095
PNG
(1,1-Dioxo-hexahydro-1lambda*6*-thiopyran-4-carboxy...)
Show SMILES Cc1nc2ccc(F)cc2n1C1C[C@@H]2CC[C@H](C1)N2CC[C@H](NC(=O)C1CCS(=O)(=O)CC1)c1cccc(F)c1 |r,THB:19:18:11.12.17:14.15|
Show InChI InChI=1S/C30H36F2N4O3S/c1-19-33-28-8-5-23(32)16-29(28)36(19)26-17-24-6-7-25(18-26)35(24)12-9-27(21-3-2-4-22(31)15-21)34-30(37)20-10-13-40(38,39)14-11-20/h2-5,8,15-16,20,24-27H,6-7,9-14,17-18H2,1H3,(H,34,37)/t24-,25+,26?,27-/m0/s1
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PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of human ERG


Bioorg Med Chem Lett 20: 6400-4 (2010)


Article DOI: 10.1016/j.bmcl.2010.09.089
BindingDB Entry DOI: 10.7270/Q23N23M5
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50330094
PNG
(1-Oxo-tetrahydro-thiopyran-4-carboxylic acid{1-(3-...)
Show SMILES Cc1nc2ccccc2n1C1C[C@@H]2CC[C@H](C1)N2CC[C@H](NC(=O)C1CCS(=O)CC1)c1cccc(F)c1 |r,THB:18:17:10.11.16:13.14|
Show InChI InChI=1S/C30H37FN4O2S/c1-20-32-28-7-2-3-8-29(28)35(20)26-18-24-9-10-25(19-26)34(24)14-11-27(22-5-4-6-23(31)17-22)33-30(36)21-12-15-38(37)16-13-21/h2-8,17,21,24-27H,9-16,18-19H2,1H3,(H,33,36)/t21?,24-,25+,26?,27-,38?/m0/s1
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Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of human ERG


Bioorg Med Chem Lett 20: 6400-4 (2010)


Article DOI: 10.1016/j.bmcl.2010.09.089
BindingDB Entry DOI: 10.7270/Q23N23M5
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%