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Compile Data Set for Download or QSAR

Found 2 hits of ki for monomerid = 50126918   
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
Coagulation factor IX


(Homo sapiens (Human))
BDBM50126918
PNG
(CHEMBL3629113)
Show SMILES Cc1ccc2n3C[C@@](CCc3c(C(O)=O)c2c1)(NC(=O)c1c(Cl)cc(cc1Cl)-n1cnnn1)c1ccccc1 |r|
Show InChI InChI=1S/C28H22Cl2N6O3/c1-16-7-8-22-19(11-16)24(27(38)39)23-9-10-28(14-35(22)23,17-5-3-2-4-6-17)32-26(37)25-20(29)12-18(13-21(25)30)36-15-31-33-34-36/h2-8,11-13,15H,9-10,14H2,1H3,(H,32,37)(H,38,39)/t28-/m1/s1
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PC cid
PC sid
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Similars

Article
PubMed
8.60n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human F9a using CH3SO2-D-CHG-Gly-Arg-AFC.AcOH as substrate by fluorescence assay


Bioorg Med Chem Lett 25: 5437-43 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.078
BindingDB Entry DOI: 10.7270/Q2B859X6
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50126918
PNG
(CHEMBL3629113)
Show SMILES Cc1ccc2n3C[C@@](CCc3c(C(O)=O)c2c1)(NC(=O)c1c(Cl)cc(cc1Cl)-n1cnnn1)c1ccccc1 |r|
Show InChI InChI=1S/C28H22Cl2N6O3/c1-16-7-8-22-19(11-16)24(27(38)39)23-9-10-28(14-35(22)23,17-5-3-2-4-6-17)32-26(37)25-20(29)12-18(13-21(25)30)36-15-31-33-34-36/h2-8,11-13,15H,9-10,14H2,1H3,(H,32,37)(H,38,39)/t28-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
1.05E+3n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Inhibition of human F10a using CH3SO2-D-CHG-Gly-Arg-AFC.AcOH as substrate by fluorescence assay


Bioorg Med Chem Lett 25: 5437-43 (2015)


Article DOI: 10.1016/j.bmcl.2015.07.078
BindingDB Entry DOI: 10.7270/Q2B859X6
More data for this
Ligand-Target Pair