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6 similar compounds to monomer 50144088

Compile data set for download or QSAR
Wt: 613.1
BDBM50144084
Wt: 558.0
BDBM50144106
Wt: 544.0
BDBM50144116
Wt: 529.9
BDBM50144118
Wt: 546.0
BDBM50193837
Wt: 517.9
BDBM50193853

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50144084,50144106,50144116,50144118,50193837,50193853   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/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))
BDBM50193837
PNG
((R)-4-(5-chloro-1H-indole-2-sulfonyl)-1-[4-(N,N-di...)
Show SMILES CCOC(=O)[C@H]1CN(CC(=O)N1Cc1ccc(cc1)C(=N)N(C)C)S(=O)(=O)c1cc2cc(Cl)ccc2[nH]1
Show InChI InChI=1S/C25H28ClN5O5S/c1-4-36-25(33)21-14-30(37(34,35)22-12-18-11-19(26)9-10-20(18)28-22)15-23(32)31(21)13-16-5-7-17(8-6-16)24(27)29(2)3/h5-12,21,27-28H,4,13-15H2,1-3H3/t21-/m1/s1
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71n/an/an/an/an/an/an/an/a



Portola Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]dofetilide from human ERG potassium channel expressed in HEK293 cells


Bioorg Med Chem Lett 16: 5507-12 (2006)


Article DOI: 10.1016/j.bmcl.2006.08.039
BindingDB Entry DOI: 10.7270/Q2SF2X05
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50193853
PNG
((R)-4-(5-chloro-1H-indole-2-sulfonyl)-1-[4-(N,N-di...)
Show SMILES CN(C)C(=N)c1ccc(CN2[C@H](CN(CC2=O)S(=O)(=O)c2cc3cc(Cl)ccc3[nH]2)C(O)=O)cc1
Show InChI InChI=1S/C23H24ClN5O5S/c1-27(2)22(25)15-5-3-14(4-6-15)11-29-19(23(31)32)12-28(13-21(29)30)35(33,34)20-10-16-9-17(24)7-8-18(16)26-20/h3-10,19,25-26H,11-13H2,1-2H3,(H,31,32)/t19-/m1/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



Portola Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]dofetilide from human ERG potassium channel expressed in HEK293 cells


Bioorg Med Chem Lett 16: 5507-12 (2006)


Article DOI: 10.1016/j.bmcl.2006.08.039
BindingDB Entry DOI: 10.7270/Q2SF2X05
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50144118
PNG
(4-(5-Chloro-1H-indole-2-sulfonyl)-1-[4-(1-methyl-4...)
Show SMILES CN1CCN=C1c1ccc(cc1)C(=O)N1CCN(CC1C(O)=O)S(=O)(=O)c1cc2cc(Cl)ccc2[nH]1
Show InChI InChI=1/C24H24ClN5O5S/c1-28-9-8-26-22(28)15-2-4-16(5-3-15)23(31)30-11-10-29(14-20(30)24(32)33)36(34,35)21-13-17-12-18(25)6-7-19(17)27-21/h2-7,12-13,20,27H,8-11,14H2,1H3,(H,32,33)
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n/an/a 12n/an/an/an/an/an/a



Millennium Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Coagulation factor X was determined


Bioorg Med Chem Lett 14: 2073-8 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.049
BindingDB Entry DOI: 10.7270/Q2P84B98
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50144106
PNG
(CHEMBL65146 | {4-(5-Chloro-1H-indole-2-sulfonyl)-1...)
Show SMILES COC(=O)CC1CN(CCN1C(=O)c1ccc(cc1)C1=NCCN1C)S(=O)(=O)c1cc2cc(Cl)ccc2[nH]1
Show InChI InChI=1/C26H28ClN5O5S/c1-30-10-9-28-25(30)17-3-5-18(6-4-17)26(34)32-12-11-31(16-21(32)15-24(33)37-2)38(35,36)23-14-19-13-20(27)7-8-22(19)29-23/h3-8,13-14,21,29H,9-12,15-16H2,1-2H3
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n/an/a 3n/an/an/an/an/an/a



Millennium Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Coagulation factor X was determined


Bioorg Med Chem Lett 14: 2073-8 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.049
BindingDB Entry DOI: 10.7270/Q2P84B98
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50144084
PNG
(2-{4-(5-Chloro-1H-indole-2-sulfonyl)-1-[4-(1-methy...)
Show SMILES CN1CCN=C1c1ccc(cc1)C(=O)N1CCN(CC1CC(=O)N1CCOCC1)S(=O)(=O)c1cc2cc(Cl)ccc2[nH]1
Show InChI InChI=1/C29H33ClN6O5S/c1-33-9-8-31-28(33)20-2-4-21(5-3-20)29(38)36-11-10-35(19-24(36)18-27(37)34-12-14-41-15-13-34)42(39,40)26-17-22-16-23(30)6-7-25(22)32-26/h2-7,16-17,24,32H,8-15,18-19H2,1H3
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n/an/a 11n/an/an/an/an/an/a



Millennium Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Coagulation factor X was determined


Bioorg Med Chem Lett 14: 2073-8 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.049
BindingDB Entry DOI: 10.7270/Q2P84B98
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50144116
PNG
(CHEMBL292941 | {4-(5-Chloro-1H-indole-2-sulfonyl)-...)
Show SMILES CN1CCN=C1c1ccc(cc1)C(=O)N1CCN(CC1CC(O)=O)S(=O)(=O)c1cc2cc(Cl)ccc2[nH]1
Show InChI InChI=1/C25H26ClN5O5S/c1-29-9-8-27-24(29)16-2-4-17(5-3-16)25(34)31-11-10-30(15-20(31)14-23(32)33)37(35,36)22-13-18-12-19(26)6-7-21(18)28-22/h2-7,12-13,20,28H,8-11,14-15H2,1H3,(H,32,33)
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n/an/a 41n/an/an/an/an/an/a



Millennium Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Coagulation factor X was determined


Bioorg Med Chem Lett 14: 2073-8 (2004)


Article DOI: 10.1016/j.bmcl.2004.02.049
BindingDB Entry DOI: 10.7270/Q2P84B98
More data for this
Ligand-Target Pair