Compile Data Set for Download or QSAR
Report error Found 46 Enz. Inhib. hit(s) with all data for entry = 1599
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12539BDBM12539((2S)-2-[(3S)-3-{2-[(6-chloronaphthalene-2-)sulfona...)
Affinity DataKi:  1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12540BDBM12540((2S)-N-(2-aminoethyl)-2-[(3S)-3-{2-[(6-chloronapht...)
Affinity DataKi: <1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12541BDBM12541((2S)-N-[2-(carbamoylamino)ethyl]-2-[(3S)-3-{2-[(6-...)
Affinity DataKi:  1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12542BDBM12542((2S)-2-[(3S)-3-{2-[(6-chloronaphthalene-2-)sulfona...)
Affinity DataKi: <1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12543BDBM12543((2S)-2-[(3S)-3-{2-[(6-chloronaphthalene-2-)sulfona...)
Affinity DataKi:  1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12528BDBM12528((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12544BDBM12544((2S)-2-[(3S)-3-{2-[(6-chloronaphthalene-2-)sulfona...)
Affinity DataKi:  1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12545BDBM12545((2S)-N-[2-(1H-azepin-1-yl)ethyl]-2-[(3S)-3-{2-[(6-...)
Affinity DataKi: <1nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12531BDBM12531((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12532BDBM12532((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12534BDBM12534((2S)-N-[2-(1H-azepin-1-yl)ethyl]-2-[(3S)-3-[(6-chl...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12535BDBM12535((2S)-N-(3-aminopropyl)-2-[(3S)-3-[(6-chloronaphtha...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12525BDBM12525((2S)-N-[2-(carbamoylamino)ethyl]-2-[(3S)-3-[(6-chl...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12529BDBM12529((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  2nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12537BDBM12537((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  3nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12509BDBM12509((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  3nM ΔG°:  -48.6kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12530BDBM12530((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  3nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12533BDBM12533((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  4nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12522BDBM12522((2S)-N-(2-aminoethyl)-2-[(3S)-3-[(6-chloronaphthal...)
Affinity DataKi:  4nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12536BDBM12536((2S)-N-[3-(carbamoylamino)propyl]-2-[(3S)-3-[(6-ch...)
Affinity DataKi:  5nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12506BDBM12506((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  5nM ΔG°:  -47.4kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12517BDBM12517((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  6nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12519BDBM12519((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  6nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12538BDBM12538(N-[(3S)-2-oxopyrrolidin-3-yl]sulfonamide, 1a | 6-c...)
Affinity DataKi:  6nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12520BDBM12520((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  7nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12526BDBM12526((2S)-N-[2-(carbamoylamino)ethyl]-2-[(3S)-3-[(6-chl...)
Affinity DataKi:  7nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12516BDBM12516((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  9nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12515BDBM12515((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  11nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12505BDBM12505((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  11nM ΔG°:  -45.4kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12524BDBM12524((2S)-N-(2-carbamoylethyl)-2-[(3S)-3-[(6-chloronaph...)
Affinity DataKi:  11nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12511BDBM12511((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  11nM ΔG°:  -45.4kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12518BDBM12518((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  13nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12523BDBM12523((2S)-N-(2-aminoethyl)-2-[(3S)-3-[(6-chloronaphthal...)
Affinity DataKi:  15nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12510BDBM12510((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  15nM ΔG°:  -44.7kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12504BDBM12504((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  22nM ΔG°:  -43.7kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12502BDBM12502((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  24nM ΔG°:  -43.5kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12514BDBM12514((2S)-N-benzyl-2-[(3S)-3-[(6-chloronaphthalene-2-)s...)
Affinity DataKi:  24nM ΔG°:  -43.5kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12513BDBM12513((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  27nM ΔG°:  -43.2kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12501BDBM12501((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  56nM ΔG°:  -41.4kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12508BDBM12508((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  57nM ΔG°:  -41.3kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12512BDBM12512((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  73nM ΔG°:  -40.7kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12507BDBM12507((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  136nM ΔG°:  -39.2kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12499BDBM12499((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  346nM ΔG°:  -36.9kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12503BDBM12503((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  2.72E+3nM ΔG°:  -31.8kJ/molepH: 7.8 T: 2°CAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12521BDBM12521((2S)-N-(2-aminoethyl)-2-[(3S)-3-[(6-chloronaphthal...)
Affinity DataKi:  4.10E+3nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Glaxosmithkline

LigandChemical structure of BindingDB Monomer ID 12527BDBM12527((2S)-2-[(3S)-3-[(6-chloronaphthalene-2-)sulfonamid...)
Affinity DataKi:  3.90E+4nMAssay Description:The inhibitory effect of test compound for human fXa was determined by using the chromogenic substrate. The hydrolysis rates of chromogenic substrate...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/12/2006
Entry Details Article
PubMed