Compile Data Set for Download or QSAR
Report error Found 718 of ph data with Target = 'Coagulation factor X'
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12751BDBM12751(CHEMBL152854 | 1-(3-carbamimidoylphenyl)-3-methyl-...)
Affinity DataKi:  0.0130nM ΔG°:  -61.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12751BDBM12751(CHEMBL152854 | 1-(3-carbamimidoylphenyl)-3-methyl-...)
Affinity DataKi:  0.0130nM ΔG°:  -61.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were determined ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12852BDBM12852(4-{[2-(4-{[1-(3-amino-1,2-benzoxazol-5-yl)-3-(trif...)
Affinity DataKi:  0.0200nM ΔG°:  -60.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12754BDBM12754(1-(3-carbamimidoylphenyl)-N-(2-fluoro-4-{1H-imidaz...)
Affinity DataKi:  0.0240nM ΔG°:  -60.0kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12757BDBM12757(1-(3-carbamimidoylphenyl)-N-(2-fluoro-4-{3H-imidaz...)
Affinity DataKi:  0.0280nM ΔG°:  -59.6kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12693BDBM12693(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[(3R)-3-h...)
Affinity DataKi:  0.0300nM ΔG°:  -59.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12693BDBM12693(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[(3R)-3-h...)
Affinity DataKi:  0.0300nM ΔG°:  -59.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12755BDBM12755(1-(3-carbamimidoylphenyl)-N-(2-fluoro-4-{1H-imidaz...)
Affinity DataKi:  0.0360nM ΔG°:  -59.0kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12681BDBM12681(1-(3-amino-1,2-benzoxazol-5-yl)-6-(4-{2-[(dimethyl...)
Affinity DataKi:  0.0400nM ΔG°:  -58.8kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12681BDBM12681(1-(3-amino-1,2-benzoxazol-5-yl)-6-(4-{2-[(dimethyl...)
Affinity DataKi:  0.0400nM ΔG°:  -58.8kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12756BDBM12756(1-(3-carbamimidoylphenyl)-N-(2-fluoro-4-{3H-imidaz...)
Affinity DataKi:  0.0440nM ΔG°:  -58.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12853BDBM12853({[2-(4-{[1-(3-amino-1,2-benzoxazol-5-yl)-3-(triflu...)
Affinity DataKi:  0.0500nM ΔG°:  -58.2kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12766BDBM12766(1-(3-carbamimidoylphenyl)-N-[4-(2-oxo-2,7a-dihydro...)
Affinity DataKi:  0.0580nM ΔG°:  -57.8kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 18991BDBM18991(6-[4-(2-{[(3R)-3-hydroxypyrrolidin-1-yl]methyl}phe...)
Affinity DataKi:  0.0700nM ΔG°:  -57.4kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 19023BDBM19023(BMS-562247 | CHEMBL231779 | 1-(4-methoxyphenyl)-7-...)
Affinity DataKi:  0.0750nM ΔG°:  -57.8kJ/molepH: 7.4 T: 2°CAssay Description:Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2017
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12851BDBM12851(1-{[2-(4-{[1-(3-amino-1,2-benzoxazol-5-yl)-3-(trif...)
Affinity DataKi:  0.0800nM ΔG°:  -57.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12763BDBM12763(1-(3-carbamimidoylphenyl)-N-[2-fluoro-4-(5-nitro-1...)
Affinity DataKi:  0.0800nM ΔG°:  -57.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12659BDBM12659(1-(3-amino-1,2-benzoxazol-5-yl)-N-[2-fluoro-4-(2-m...)
Affinity DataKi:  0.0900nM ΔG°:  -56.8kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12767BDBM12767(1-(3-carbamimidoylphenyl)-N-[4-(1H-imidazol-1-yl)p...)
Affinity DataKi:  0.0910nM ΔG°:  -56.7kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12752BDBM12752(N-[4-(1H-1,3-benzodiazol-1-yl)phenyl]-1-(3-carbami...)
Affinity DataKi:  0.0940nM ΔG°:  -56.7kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12840BDBM12840(1-(3-amino-1,2-benzoxazol-5-yl)-N-{2-fluoro-4-[2-(...)
Affinity DataKi:  0.100nM ΔG°:  -56.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12661BDBM12661(Razaxaban Analogue | 1-(3-amino-1,2-benzoxazol-5-y...)
Affinity DataKi:  0.100nM ΔG°:  -56.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12690BDBM12690(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[ethyl(me...)
Affinity DataKi: <0.100nM ΔG°: <-56.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12753BDBM12753(N-[4-(1H-1,3-benzodiazol-1-yl)-2-fluorophenyl]-1-(...)
Affinity DataKi:  0.100nM ΔG°:  -56.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 17284BDBM17284(2-{[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-diflu...)
Affinity DataKi:  0.110nM ΔG°:  -56.3kJ/molepH: 7.5 T: 2°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2007
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 17280BDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  0.110nM ΔG°:  -56.3kJ/molepH: 7.5 T: 2°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12870BDBM12870(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[(3R)-3-h...)
Affinity DataKi:  0.110nM ΔG°:  -56.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 17280BDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  0.110nM ΔG°:  -56.3kJ/molepH: 7.5 T: 2°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/16/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12689BDBM12689(bicyclic pyrazole scaffold | 1-(3-amino-1,2-benzox...)
Affinity DataKi:  0.110nM ΔG°:  -56.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12694BDBM12694(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[(3S)-3-h...)
Affinity DataKi:  0.120nM ΔG°:  -56.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12762BDBM12762(N-[4-(5-amino-1H-1,3-benzodiazol-1-yl)-2-fluorophe...)
Affinity DataKi:  0.120nM ΔG°:  -56.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12748BDBM12748(2-{6-[4-(2-methanesulfonylphenyl)phenyl]-7-oxo-3-(...)
Affinity DataKi:  0.120nM ΔG°:  -56.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12682BDBM12682(bicyclic pyrazole scaffold | 1-(3-amino-1,2-benzox...)
Affinity DataKi:  0.130nM ΔG°:  -55.9kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 19023BDBM19023(BMS-562247 | CHEMBL231779 | 1-(4-methoxyphenyl)-7-...)
Affinity DataKi:  0.140nM ΔG°:  -57.4kJ/molepH: 7.4 T: 2°CAssay Description:Inhibition of peptide substrate cleavage by FXa was assayed against six concentrations of S2765 and six concentrations of apixaban. Typical assays we...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2017
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12657BDBM12657(CHEMBL559015 | 1-[3-(Aminomethyl)phenyl]-N-[3-fluo...)
Affinity DataKi:  0.150nM ΔG°:  -55.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12846BDBM12846(1-(3-amino-1,2-benzoxazol-5-yl)-N-{2-fluoro-4-[2-(...)
Affinity DataKi:  0.150nM ΔG°:  -55.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12692BDBM12692(1-(3-amino-1,2-benzoxazol-5-yl)-6-{4-[2-(pyrrolidi...)
Affinity DataKi:  0.150nM ΔG°:  -55.5kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12700BDBM12700(1-(3-amino-1,2-benzoxazol-5-yl)-6-[2-fluoro-4-(2-{...)
Affinity DataKi:  0.160nM ΔG°:  -55.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 17088BDBM17088(3-chloro-N-{4-chloro-2-[(5-chloropyridin-2-yl)carb...)
Affinity DataKi:  0.160nM ΔG°:  -55.3kJ/molepH: 7.5 T: 2°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/8/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12842BDBM12842(1-(3-amino-1,2-benzoxazol-5-yl)-N-[2-fluoro-4-(2-{...)
Affinity DataKi:  0.160nM ΔG°:  -55.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12660BDBM12660(1-(3-amino-1,2-benzoxazol-5-yl)-N-[2-fluoro-4-(2-s...)
Affinity DataKi:  0.160nM ΔG°:  -55.3kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12675BDBM12675(Razaxaban Analogue | 1-(3-amino-1,2-benzoxazol-5-y...)
Affinity DataKi:  0.170nM ΔG°:  -55.2kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12864BDBM12864(1-(3-amino-1,2-benzoxazol-5-yl)-6-(4-{2-[(dimethyl...)
Affinity DataKi:  0.170nM ΔG°:  -55.2kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12866BDBM12866(1-(3-amino-1,2-benzoxazol-5-yl)-6-[4-(2-{[(3R)-3-h...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/2/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 17099BDBM17099(3-chloro-N-{4-chloro-2-[(5-chloropyridin-2-yl)carb...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.5 T: 2°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/8/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12746BDBM12746(6-[4-(2-methanesulfonylphenyl)phenyl]-1-(4-methoxy...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12747BDBM12747(2-{6-[4-(2-methanesulfonylphenyl)phenyl]-7-oxo-3-(...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12733BDBM12733(3-[6-(4-{2-[(dimethylamino)methyl]phenyl}phenyl)-7...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/19/2006
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12743BDBM12743(6-[4-(2-{[(3R)-3-hydroxypyrrolidin-1-yl]methyl}phe...)
Affinity DataKi:  0.180nM ΔG°:  -55.1kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2007
Entry Details Article
PubMed
TargetCoagulation factor X(Human)
Bristol Myers Squibb

LigandChemical structure of BindingDB Monomer ID 12676BDBM12676(DPC 906 | 1-(3-Aminobenzisoxazol-5-yl)-3-trifluoro...)
Affinity DataKi:  0.190nM ΔG°:  -54.9kJ/molepH: 7.0 T: 2°CAssay Description:Ki values were obtained from human purified enzyme. All assays were run in microtiter plates. Plates were read for 30 min at 405 nm. Rates were deter...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/1/2007
Entry Details Article
PubMed
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