Compile Data Set for Download or QSAR
Report error Found 58 Enz. Inhib. hit(s) with all data for entry = 50014788
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147416BDBM50147416(3-(4-Chloro-1-guanidino-isoquinolin-7-yl)-4-methox...)
Affinity DataKi:  9nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147422BDBM50147422(3-(4-Chloro-1-guanidino-isoquinolin-7-yl)-benzoic ...)
Affinity DataKi:  37nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147424BDBM50147424(4-(4-Chloro-1-guanidino-isoquinolin-7-yl)-benzoic ...)
Affinity DataKi:  82nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147419BDBM50147419(N-[4-Chloro-7-(3-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  83nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147423BDBM50147423(N-(7-Benzo[1,3]dioxol-5-yl-4-chloro-isoquinolin-1-...)
Affinity DataKi:  100nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147418BDBM50147418(N-[4-Chloro-7-(2-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  100nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147415BDBM50147415(N-(4-Chloro-7-p-tolyl-isoquinolin-1-yl)-guanidine ...)
Affinity DataKi:  130nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147409BDBM50147409(N-[4-Chloro-7-(5-cyano-2-methoxy-phenyl)-isoquinol...)
Affinity DataKi:  180nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147404BDBM50147404(N-[4-Chloro-7-(4-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  200nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147417BDBM50147417(N-[4-Chloro-7-(3-cyano-phenyl)-isoquinolin-1-yl]-g...)
Affinity DataKi:  300nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147414BDBM50147414(N-(4-Chloro-7-phenyl-isoquinolin-1-yl)-guanidine |...)
Affinity DataKi:  310nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147429BDBM50147429(N-(7-Benzo[1,3]dioxol-5-yl-isoquinolin-1-yl)-guani...)
Affinity DataKi:  340nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147402BDBM50147402(N-(7-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL32...)
Affinity DataKi:  400nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147413BDBM50147413(N-[4-Chloro-7-(4-cyano-phenyl)-isoquinolin-1-yl]-g...)
Affinity DataKi:  490nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147420BDBM50147420(N-(4-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL323...)
Affinity DataKi:  580nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147408BDBM50147408(N-[7-(1-Hydroxy-ethyl)-isoquinolin-1-yl]-guanidine...)
Affinity DataKi:  640nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147407BDBM50147407(N-(7-Methoxy-isoquinolin-1-yl)-guanidine | CHEMBL1...)
Affinity DataKi:  660nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147406BDBM50147406(N-(7-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL321...)
Affinity DataKi:  800nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147410BDBM50147410(N-(4-Chloro-isoquinolin-1-yl)-guanidine | CHEMBL32...)
Affinity DataKi:  830nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147427BDBM50147427(1-Guanidino-isoquinoline-7-carboxylic acid | CHEMB...)
Affinity DataKi:  1.00E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147405BDBM50147405(N-(7-Hydroxymethyl-isoquinolin-1-yl)-guanidine | C...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147431BDBM50147431(N-(4-Methyl-isoquinolin-1-yl)-guanidine | CHEMBL11...)
Affinity DataKi:  1.40E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147412BDBM50147412(N-Isoquinolin-1-yl-guanidine | CHEMBL321822)
Affinity DataKi:  1.92E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147403BDBM50147403(N-(6-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL107...)
Affinity DataKi:  2.34E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147404BDBM50147404(N-[4-Chloro-7-(4-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147423BDBM50147423(N-(7-Benzo[1,3]dioxol-5-yl-4-chloro-isoquinolin-1-...)
Affinity DataKi:  3.20E+3nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147432BDBM50147432(N-(5-Methoxy-isoquinolin-1-yl)-guanidine | CHEMBL3...)
Affinity DataKi:  3.62E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147417BDBM50147417(N-[4-Chloro-7-(3-cyano-phenyl)-isoquinolin-1-yl]-g...)
Affinity DataKi:  4.10E+3nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147416BDBM50147416(3-(4-Chloro-1-guanidino-isoquinolin-7-yl)-4-methox...)
Affinity DataKi:  4.75E+3nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147411BDBM50147411(N-(5-Benzyloxy-isoquinolin-1-yl)-guanidine | CHEMB...)
Affinity DataKi:  4.80E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147425BDBM50147425(N-(7-Benzyloxy-isoquinolin-1-yl)-guanidine | CHEMB...)
Affinity DataKi:  4.80E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147428BDBM50147428(N-(5-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL110...)
Affinity DataKi:  4.93E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147415BDBM50147415(N-(4-Chloro-7-p-tolyl-isoquinolin-1-yl)-guanidine ...)
Affinity DataKi:  7.30E+3nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147430BDBM50147430(N-Isoquinolin-3-yl-guanidine | CHEMBL109632)
Affinity DataKi:  9.30E+3nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147429BDBM50147429(N-(7-Benzo[1,3]dioxol-5-yl-isoquinolin-1-yl)-guani...)
Affinity DataKi:  1.20E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147411BDBM50147411(N-(5-Benzyloxy-isoquinolin-1-yl)-guanidine | CHEMB...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147425BDBM50147425(N-(7-Benzyloxy-isoquinolin-1-yl)-guanidine | CHEMB...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147418BDBM50147418(N-[4-Chloro-7-(2-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  1.45E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147418BDBM50147418(N-[4-Chloro-7-(2-methoxy-phenyl)-isoquinolin-1-yl]...)
Affinity DataKi:  1.55E+4nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147415BDBM50147415(N-(4-Chloro-7-p-tolyl-isoquinolin-1-yl)-guanidine ...)
Affinity DataKi:  1.90E+4nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147408BDBM50147408(N-[7-(1-Hydroxy-ethyl)-isoquinolin-1-yl]-guanidine...)
Affinity DataKi:  2.40E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50053618BDBM50053618(N-Pyridin-2-yl-guanidine | CHEMBL128047)
Affinity DataKi:  2.90E+4nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147402BDBM50147402(N-(7-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL32...)
Affinity DataKi:  4.75E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147426BDBM50147426(N-(5-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL11...)
Affinity DataKi:  4.75E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147406BDBM50147406(N-(7-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL321...)
Affinity DataKi:  5.08E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetPlasminogen(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147412BDBM50147412(N-Isoquinolin-1-yl-guanidine | CHEMBL321822)
Affinity DataKi:  6.80E+4nMAssay Description:Inhibitory activity against human plasmin was evaluated using chromozym-PL as substrate at 1 mMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147406BDBM50147406(N-(7-Bromo-isoquinolin-1-yl)-guanidine | CHEMBL321...)
Affinity DataKi:  9.51E+4nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetUrokinase-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147426BDBM50147426(N-(5-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL11...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibitory activity against human urokinase-type plasminogen activator was evaluated using S-2444 as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147426BDBM50147426(N-(5-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL11...)
Affinity DataKi:  1.24E+5nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTissue-type plasminogen activator(Human)
Pfizer

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50147402BDBM50147402(N-(7-Phenyl-isoquinolin-1-yl)-guanidine | CHEMBL32...)
Affinity DataKi:  1.24E+5nMAssay Description:Inhibitory activity against human tissue type plasminogen activator using S-2444More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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