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Compile Data Set for Download or QSAR

Found 6 hits of Enz. Inhib. data with enzyme = 'Coagulation factor X' and Substrate = 'BDBM234442'   
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
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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0.0750 -13.8n/an/an/an/an/a7.425



Bristol-Myers Squibb Company



Assay Description
Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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0.140 -13.7n/an/an/an/an/a7.431



Bristol-Myers Squibb Company



Assay Description
Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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0.25 -13.6n/an/an/an/an/a7.437



Bristol-Myers Squibb Company



Assay Description
Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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PubMed
0.400 -13.6n/an/an/an/an/a7.443



Bristol-Myers Squibb Company



Assay Description
Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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Article
PubMed
0.410 -12.8n/an/an/an/an/a7.525



Bristol-Myers Squibb Company



Assay Description
For comparison with the prothrombinase reaction the assays were also conducted with S2765 at 25 and 37C in a similar buffer: 20 mM HEPES, pH 7.5 con...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Coagulation factor X


(Homo sapiens (human))
BDBM19023
PNG
(1-(4-methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-y...)
Show SMILES COc1ccc(cc1)-n1nc(C(N)=O)c2CCN(C(=O)c12)c1ccc(cc1)N1CCCCC1=O
Show InChI InChI=1S/C25H25N5O4/c1-34-19-11-9-18(10-12-19)30-23-20(22(27-30)24(26)32)13-15-29(25(23)33)17-7-5-16(6-8-17)28-14-3-2-4-21(28)31/h5-12H,2-4,13-15H2,1H3,(H2,26,32)
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Article
PubMed
0.720 -13.0n/an/an/an/an/a7.537



Bristol-Myers Squibb Company



Assay Description
For comparison with the prothrombinase reaction the assays were also conducted with S2765 at 25 and 37C in a similar buffer: 20 mM HEPES, pH 7.5 con...


J Enzyme Inhib Med Chem 26: 514-26 (2011)


Article DOI: 10.3109/14756366.2010.535793
BindingDB Entry DOI: 10.7270/Q2VX0FDF
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)