Compile Data Set for Download or QSAR
Report error Found 49 of affinity data for UniProtKB/TrEMBL: P10210
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59224BDBM59224(Pepstatin analog, 12)
Affinity DataKi:  96nM IC50: 360nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59223BDBM59223(Pepstatin analog, 11)
Affinity DataKi:  175nM IC50: 730nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59213BDBM59213(Pepstatin analog, 1)
Affinity DataKi:  220nM IC50: 350nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289659BDBM50289659([(S)-1-(4-Oxo-4H-thieno[3,2-d][1,3]oxazin-2-yl)-et...)
Affinity DataIC50: 480nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59220BDBM59220(Pepstatin analog, 8)
Affinity DataKi:  600nM IC50: 2.90E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59222BDBM59222(Pepstatin analog, 10)
Affinity DataKi:  650nM IC50: 2.50E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289663BDBM50289663([(S)-2-Hydroxy-1-(4-oxo-4H-thieno[3,2-d][1,3]oxazi...)
Affinity DataIC50: 650nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59219BDBM59219(Pepstatin analog, 7)
Affinity DataKi:  720nM IC50: 2.70E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59216BDBM59216(Pepstatin analog, 4)
Affinity DataKi:  1.13E+3nM IC50: 4.40E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59217BDBM59217(Pepstatin analog, 5)
Affinity DataKi:  1.29E+3nM IC50: 4.90E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288088BDBM50288088(5,8-Dichloro-2-ethoxy-benzo[d][1,3]oxazin-4-one | ...)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288091BDBM50288091(2-(4-Methoxy-phenoxy)-benzo[d][1,3]oxazin-4-one | ...)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289665BDBM50289665((4-Oxo-4H-thieno[3,2-d][1,3]oxazin-2-ylmethyl)-car...)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59214BDBM59214(Pepstatin analog, 2)
Affinity DataKi:  3.00E+3nM IC50: 5.90E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289660BDBM50289660([(S)-1-(7-Methyl-4-oxo-4H-thieno[3,2-d][1,3]oxazin...)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289664BDBM50289664([(S)-1-(4-Oxo-6-phenyl-4H-thieno[3,2-d][1,3]oxazin...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59221BDBM59221(Pepstatin analog, 9)
Affinity DataIC50: 4.30E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288097BDBM50288097([1-(2-Isopropylamino-4-oxo-4H-benzo[d][1,3]oxazin-...)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59215BDBM59215(Pepstatin analog, 3)
Affinity DataIC50: 5.80E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 59218BDBM59218(Pepstatin analog, 6)
Affinity DataIC50: 5.80E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/27/2011
Entry Details Article
PubMed
TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289666BDBM50289666([(S)-3-Carbamoyl-1-(4-oxo-4H-thieno[3,2-d][1,3]oxa...)
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288096BDBM50288096(5-Chloro-2-ethoxy-benzo[d][1,3]oxazin-4-one | CHEM...)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289658BDBM50289658([(S)-2-Carbamoyl-1-(4-oxo-4H-thieno[3,2-d][1,3]oxa...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288086BDBM50288086(2-Phenoxy-benzo[d][1,3]oxazin-4-one | CHEMBL81468)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288079BDBM50288079({(S)-1-[7-(2-Benzyloxycarbonylamino-propionylamino...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288082BDBM50288082([2-Carbamoyl-1-(2-isopropylamino-4-oxo-4H-benzo[d]...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288087BDBM50288087(2-Ethoxy-5-methyl-benzo[d][1,3]oxazin-4-one | CHEM...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288093BDBM50288093(2-Allyloxy-benzo[d][1,3]oxazin-4-one | CHEMBL81469)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288098BDBM50288098(2-Ethoxy-5-ethyl-benzo[d][1,3]oxazin-4-one | CHEMB...)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288095BDBM50288095(2-Ethoxy-benzo[d][1,3]oxazin-4-one | CHEMBL450273)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288083BDBM50288083(2-Isopropylamino-benzo[d][1,3]oxazin-4-one | CHEMB...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288089BDBM50288089(2-(4-Oxo-4H-benzo[d][1,3]oxazin-2-ylamino)-propion...)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289661BDBM50289661([(S)-2-Methyl-1-(4-oxo-4H-thieno[3,2-d][1,3]oxazin...)
Affinity DataIC50: 3.10E+4nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288081BDBM50288081((2-Isopropylamino-4-oxo-4H-benzo[d][1,3]oxazin-7-y...)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288084BDBM50288084([(S)-1-(4-Oxo-4H-benzo[d][1,3]oxazin-2-yl)-ethyl]-...)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288084BDBM50288084([(S)-1-(4-Oxo-4H-benzo[d][1,3]oxazin-2-yl)-ethyl]-...)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288092BDBM50288092([(S)-1-(5-Fluoro-4-oxo-4H-benzo[d][1,3]oxazin-2-yl...)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288085BDBM50288085(7-Amino-2-isopropylamino-benzo[d][1,3]oxazin-4-one...)
Affinity DataIC50: 5.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288103BDBM50288103(2-(1-Phenyl-ethylamino)-benzo[d][1,3]oxazin-4-one ...)
Affinity DataIC50: 6.00E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288099BDBM50288099(2-Ethoxy-5-fluoro-benzo[d][1,3]oxazin-4-one | CHEM...)
Affinity DataIC50: 7.50E+4nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288102BDBM50288102([(S)-1-(5-Methyl-4-oxo-4H-benzo[d][1,3]oxazin-2-yl...)
Affinity DataIC50: 1.20E+5nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288102BDBM50288102([(S)-1-(5-Methyl-4-oxo-4H-benzo[d][1,3]oxazin-2-yl...)
Affinity DataIC50: 1.20E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288100BDBM50288100([(S)-1-(7-Amino-4-oxo-4H-benzo[d][1,3]oxazin-2-yl)...)
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288094BDBM50288094([(R)-1-(5-Fluoro-4-oxo-4H-benzo[d][1,3]oxazin-2-yl...)
Affinity DataIC50: 2.00E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288080BDBM50288080([(S)-1-(5-Ethyl-4-oxo-4H-benzo[d][1,3]oxazin-2-yl)...)
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288078BDBM50288078(2-(3-Fluoro-phenylamino)-benzo[d][1,3]oxazin-4-one...)
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288101BDBM50288101(2-Butylamino-benzo[d][1,3]oxazin-4-one | CHEMBL799...)
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50289662BDBM50289662([(S)-1-(4-Oxo-4H-thieno[3,2-d][1,3]oxazin-2-yl)-2-...)
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory concentration for peptidolytic activity against herpes simplex type-1 (HSV-1) protease at 10 uM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article

TargetCapsid scaffolding protein(HHV-1)
Purdue University

LigandChemical structure of BindingDB Monomer ID 50288090BDBM50288090([(S)-1-(5-Chloro-4-oxo-4H-benzo[d][1,3]oxazin-2-yl...)
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory activity against herpes simplex type 1 protease (HSV-1 pr).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/21/2010
Entry Details Article