Compile Data Set for Download or QSAR
Report error Found 472 of ph data with Target = 'Cytochrome P450 3A4'
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 144637BDBM144637(US8952036, Ex. 5)
Affinity DataIC50: 0.0503nMpH: 7.4 T: 2°CAssay Description:The standard assay conditions for the in vitro HTRF assay consisted of a 50 ul total reaction volume in black 384-well Costar polypropylene plates in...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/29/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50448963BDBM50448963(CHEMBL3125537 | US9296736, 351 | US9593129, Exampl...)
Affinity DataIC50: 0.0962nMpH: 7.4 T: 2°CAssay Description:The standard assay conditions for the in vitro HTRF assay consisted of a 50 ul total reaction volume in black 384-well Costar polypropylene plates in...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/29/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 144636BDBM144636(US8952036, Ex. 4)
Affinity DataIC50: 0.102nMpH: 7.4 T: 2°CAssay Description:The standard assay conditions for the in vitro HTRF assay consisted of a 50 ul total reaction volume in black 384-well Costar polypropylene plates in...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/29/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 144638BDBM144638(US8952036, Ex. 3)
Affinity DataIC50: 0.330nMpH: 7.4 T: 2°CAssay Description:The standard assay conditions for the in vitro HTRF assay consisted of a 50 ul total reaction volume in black 384-well Costar polypropylene plates in...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/29/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50008760BDBM50008760(CHEMBL3236364)
Affinity DataIC50: 1.83nMpH: 7.4 T: 2°CAssay Description:The standard assay conditions for the in vitro HTRF assay consisted of a 50 ul total reaction volume in black 384-well Costar polypropylene plates in...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/29/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 151585BDBM151585(US8987315, Ketoconazole | US9180183, Ketoconazole ...)
Affinity DataIC50: 20nMpH: 7.4Assay Description:Specific aspects of the incubation conditions for each assay (e.g., protein concentration, incubation time, etc.) are defined in Walsky & Obach, 2004...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/10/2018
Entry Details
US Patent
PDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 151585BDBM151585(US8987315, Ketoconazole | US9180183, Ketoconazole ...)
Affinity DataIC50: 20nMpH: 7.4Assay Description:Specific aspects of the incubation conditions for each assay (e.g., protein concentration, incubation time, etc.) are defined in Walsky & Obach, 2004...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/10/2018
Entry Details
US Patent
PDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50220136BDBM50220136(CHEMBL1471 | 5-(((2R,3S)-2-((R)-1-(3,5-bis(trifluo...)
Affinity DataIC50: 20nMpH: 7.4 T: 2°CAssay Description:A dimethyl sulfoxide (DMSO) solution of a test compound with a concentration 1000 times higher than the evaluation concentration was prepared, and a ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2019
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50220136BDBM50220136(CHEMBL1471 | 5-(((2R,3S)-2-((R)-1-(3,5-bis(trifluo...)
Affinity DataIC50: 20nMpH: 7.4 T: 2°CAssay Description:A dimethyl sulfoxide (DMSO) solution of a test compound with a concentration 1000 times higher than the evaluation concentration was prepared, and a ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/30/2018
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 119128BDBM119128(GS7)
Affinity DataKd:  40nMpH: 7.4Assay Description:Ligand binidng to CYP3A4 was monitored in 50 mM phosphate (pH 7.4) containing 20% glycerol and 1 mM DTT. The protein was titrated with small aliquots...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21164BDBM21164(1-[2-(4-methoxyphenyl)-2-[3-(4-methoxyphenyl)propo...)
Affinity DataIC50: 45nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 27879BDBM27879(CHEMBL401930 | 4-{[(2S)-2-(3-chlorophenyl)-2-hydro...)
Affinity DataIC50: 50nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a dealkylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Befo...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/6/2009
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21170BDBM21170(1-[2-(2,4-dichlorophenoxy)-2-(2,4-dichlorophenyl)e...)
Affinity DataIC50: 60nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21160BDBM21160(N-[(5-methylpyrimidin-2-yl)methyl]-6-phenyl-2-(pyr...)
Affinity DataIC50: 71nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21165BDBM21165(1-{[4-bromo-2-(2,4-dichlorophenyl)oxolan-2-yl]meth...)
Affinity DataIC50: 130nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 119129BDBM119129(GS8)
Affinity DataKd:  160nMpH: 7.4Assay Description:Ligand binidng to CYP3A4 was monitored in 50 mM phosphate (pH 7.4) containing 20% glycerol and 1 mM DTT. The protein was titrated with small aliquots...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21166BDBM21166(1-{[2-(2,4-dichlorophenyl)-4-ethyl-1,3-dioxolan-2-...)
Affinity DataIC50: 210nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21162BDBM21162(4-{1-[(2,4-dichlorophenyl)methyl]-1H-pyrazol-4-yl}...)
Affinity DataIC50: 230nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50381698BDBM50381698(CHEMBL1969102 | US8722890, 6)
Affinity DataIC50: 300nMpH: 7.4 T: 2°CAssay Description:Assays (200 μL final volume) were carried out in NUNC polypropylene deep well plates in 50 mM potassium phosphate buffer, pH 7.4, using a microt...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 183991BDBM183991(US9150566, 28)
Affinity DataIC50: 300nMpH: 7.4 T: 2°CAssay Description:The CYP3A4 inhibition assay was performed using human liver microsomes and testosterone 6'-hydroxylation as a P450 isoform-specific marker. In a tota...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2016
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 119126BDBM119126(GS5)
Affinity DataKd:  400nMpH: 7.4Assay Description:Ligand binidng to CYP3A4 was monitored in 50 mM phosphate (pH 7.4) containing 20% glycerol and 1 mM DTT. The protein was titrated with small aliquots...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2014
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 184155BDBM184155(US9150566, 193)
Affinity DataIC50: 600nMpH: 7.4 T: 2°CAssay Description:The CYP3A4 inhibition assay was performed using human liver microsomes and testosterone 6'-hydroxylation as a P450 isoform-specific marker. In a tota...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2016
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 50381698BDBM50381698(CHEMBL1969102 | US8722890, 6)
Affinity DataIC50: 760nMpH: 7.4 T: 2°CAssay Description:Assays (200 μL final volume) were carried out in NUNC polypropylene deep well plates in 50 mM potassium phosphate buffer, pH 7.4, using a microt...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/20/2014
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143070BDBM143070(US8940739, F-29)
Affinity DataIC50: 1.10E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 183967BDBM183967(US9150566, 4)
Affinity DataIC50: 1.20E+3nMpH: 7.4 T: 2°CAssay Description:The CYP3A4 inhibition assay was performed using human liver microsomes and testosterone 6'-hydroxylation as a P450 isoform-specific marker. In a tota...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2016
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 184006BDBM184006(US9150566, 43)
Affinity DataIC50: 1.20E+3nMpH: 7.4 T: 2°CAssay Description:The CYP3A4 inhibition assay was performed using human liver microsomes and testosterone 6'-hydroxylation as a P450 isoform-specific marker. In a tota...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2016
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21149BDBM21149(4-[5-(benzylsulfanyl)-4-(4-bromophenyl)-4H-1,2,4-t...)
Affinity DataIC50: 1.30E+3nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21157BDBM21157(4-(methanesulfonylmethyl)-2-(pyridin-4-yl)-6-(pyrr...)
Affinity DataIC50: 1.30E+3nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 292013BDBM292013(US10100030, Example 8)
Affinity DataIC50: 1.40E+3nMpH: 7.4 T: 2°CAssay Description:A dimethyl sulfoxide (DMSO) solution of a test compound with a concentration 1000 times higher than the evaluation concentration was prepared, and a ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2019
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 119125BDBM119125(GS4)
Affinity DataKd:  1.50E+3nMpH: 7.4Assay Description:Ligand binidng to CYP3A4 was monitored in 50 mM phosphate (pH 7.4) containing 20% glycerol and 1 mM DTT. The protein was titrated with small aliquots...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 21168BDBM21168(methyl (2S)-2-(benzylamino)-3-(1H-imidazol-4-yl)pr...)
Affinity DataIC50: 1.50E+3nMpH: 7.4 T: 2°CAssay Description:The inhibition of recombinant human CYP3A4 was measured as the ability to perform a debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin (BFC). Bef...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/7/2008
Entry Details Article
PubMed
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142935BDBM142935(US8940739, D-5)
Affinity DataIC50: 1.76E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 184007BDBM184007(US9150566, 44)
Affinity DataIC50: 2.00E+3nMpH: 7.4 T: 2°CAssay Description:The CYP3A4 inhibition assay was performed using human liver microsomes and testosterone 6'-hydroxylation as a P450 isoform-specific marker. In a tota...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2016
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143053BDBM143053(US8940739, F-10)
Affinity DataIC50: 2.01E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143079BDBM143079(US8940739, F-47)
Affinity DataIC50: 2.05E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143173BDBM143173(US8940739, H-6)
Affinity DataIC50: 2.09E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143035BDBM143035(US8940739, E-65)
Affinity DataIC50: 2.11E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142939BDBM142939(US8940739, D-14)
Affinity DataIC50: 2.13E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143102BDBM143102(US8940739, G-5)
Affinity DataIC50: 2.16E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143080BDBM143080(US8940739, F-48)
Affinity DataIC50: 2.18E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142964BDBM142964(US8940739, D-59)
Affinity DataIC50: 2.19E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142982BDBM142982(US8940739, D-96)
Affinity DataIC50: 2.19E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 261489BDBM261489(US9708266, 12 | US10011568, Ex. No. 12)
Affinity DataIC50: 2.20E+3nMpH: 7.4 T: 2°CAssay Description:A dimethyl sulfoxide (DMSO) solution of a test compound with a concentration 1000 times higher than the evaluation concentration was prepared, and a ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/30/2018
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143019BDBM143019(US8940739, E-47)
Affinity DataIC50: 2.20E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143135BDBM143135(US8940739, G-38)
Affinity DataIC50: 2.21E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143031BDBM143031(US8940739, E-61)
Affinity DataIC50: 2.23E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142993BDBM142993(US8940739, E-7)
Affinity DataIC50: 2.24E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 142960BDBM142960(US8940739, D-55)
Affinity DataIC50: 2.26E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 119127BDBM119127(GS6)
Affinity DataKd:  2.30E+3nMpH: 7.4Assay Description:Ligand binidng to CYP3A4 was monitored in 50 mM phosphate (pH 7.4) containing 20% glycerol and 1 mM DTT. The protein was titrated with small aliquots...More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/4/2014
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetCytochrome P450 3A4(Human)
Amgen

US Patent
LigandChemical structure of BindingDB Monomer ID 143125BDBM143125(US8940739, G-28)
Affinity DataIC50: 2.32E+3nMpH: 7.4Assay Description:This assay was performed in a 200 l volume in 96-well microtiter plates using cDNA-expressed human hepatic CYP3A4 (supersome, BD Gentest #456202). As...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2015
Entry Details
US Patent

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