Compile Data Set for Download or QSAR
maximum 50k data
Found 31 Enz. Inhib. hit(s) with all data for entry = 50011587
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108380(3-[(E)-2-(5-Chloro-2-guanidino-pyridin-3-yl)-vinyl...)
Affinity DataKi:  170nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108374(CHEMBL57779 | N-[3-((E)-2-Benzo[1,3]dioxol-5-yl-vi...)
Affinity DataKi:  490nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108378(CHEMBL55653 | N-[5-Chloro-3-((E)-styryl)-pyridin-2...)
Affinity DataKi:  550nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108376(CHEMBL54894 | N-{5-Chloro-3-[(E)-2-(4-methoxy-phen...)
Affinity DataKi:  690nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108386(CHEMBL53448 | N-[5-Chloro-3-((E)-2-cyclohexyl-viny...)
Affinity DataKi:  730nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108385((E)-N-Benzyl-3-(5-chloro-2-guanidino-pyridin-3-yl)...)
Affinity DataKi:  770nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108371(CHEMBL300030 | N-(5-Chloro-3-phenylethynyl-pyridin...)
Affinity DataKi:  770nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108379(CHEMBL301324 | N-(3-Benzyloxy-5-chloro-pyridin-2-y...)
Affinity DataKi:  920nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108382((E)-3-(5-Chloro-2-guanidino-pyridin-3-yl)-N-methyl...)
Affinity DataKi:  1.28E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108372((E)-3-(5-Chloro-2-guanidino-pyridin-3-yl)-acrylic ...)
Affinity DataKi:  1.50E+3nMAssay Description:Ability to inhibit HWMT human microPa using S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108373(CHEMBL55256 | N-[5-Chloro-3-((E)-2-pyridin-2-yl-vi...)
Affinity DataKi:  1.60E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108384((E)-N-Benzyl-3-(5-chloro-2-guanidino-pyridin-3-yl)...)
Affinity DataKi:  2.00E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108381(CHEMBL291726 | N-[5-Chloro-3-((E)-3-morpholin-4-yl...)
Affinity DataKi:  2.10E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108370(CHEMBL53946 | N-(5-Chloro-3-phenoxy-pyridin-2-yl)-...)
Affinity DataKi:  2.13E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108360(CHEMBL55125 | N-(3-Bromo-5-chloro-pyridin-2-yl)-gu...)
Affinity DataKi:  4.83E+3nMAssay Description:Ability to inhibit Urokinase-type plasminogen activator using HWMT human microPa (calbiochem) and S-2444 (quadratech) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108375(3-(5-Chloro-2-guanidino-pyridin-3-yl)-propionic ac...)
Affinity DataKi:  9.31E+3nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108383(CHEMBL54827 | N-Benzyl-2-(5-chloro-2-guanidino-pyr...)
Affinity DataKi:  1.61E+4nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108369(CHEMBL54415 | N-[5-Chloro-3-(2-methoxy-ethoxy)-pyr...)
Affinity DataKi:  1.64E+4nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108376(CHEMBL54894 | N-{5-Chloro-3-[(E)-2-(4-methoxy-phen...)
Affinity DataKi:  4.25E+4nMAssay Description:Ability to inhibit plasmin using human plasmin (quadratech) and Chromozym-PL (boehringer) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108380(3-[(E)-2-(5-Chloro-2-guanidino-pyridin-3-yl)-vinyl...)
Affinity DataKi:  5.20E+4nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108378(CHEMBL55653 | N-[5-Chloro-3-((E)-styryl)-pyridin-2...)
Affinity DataKi:  5.38E+4nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108376(CHEMBL54894 | N-{5-Chloro-3-[(E)-2-(4-methoxy-phen...)
Affinity DataKi:  6.01E+4nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108371(CHEMBL300030 | N-(5-Chloro-3-phenylethynyl-pyridin...)
Affinity DataKi:  6.59E+4nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108386(CHEMBL53448 | N-[5-Chloro-3-((E)-2-cyclohexyl-viny...)
Affinity DataKi:  7.15E+4nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108387((5-Chloro-2-guanidino-pyridin-3-yloxy)-acetic acid...)
Affinity DataKi:  9.02E+4nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108377(CHEMBL56959 | N-(5-Chloro-3-phenyl-pyridin-2-yl)-g...)
Affinity DataKi:  1.66E+5nMAssay Description:In vitro inhibition of human urokinase Plasminogen Activator.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108371(CHEMBL300030 | N-(5-Chloro-3-phenylethynyl-pyridin...)
Affinity DataKi:  2.18E+5nMAssay Description:Ability to inhibit plasmin using human plasmin (quadratech) and Chromozym-PL (boehringer) as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108373(CHEMBL55256 | N-[5-Chloro-3-((E)-2-pyridin-2-yl-vi...)
Affinity DataKi:  2.59E+5nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108360(CHEMBL55125 | N-(3-Bromo-5-chloro-pyridin-2-yl)-gu...)
Affinity DataKi:  2.72E+5nMAssay Description:Ability to inhibit Tissue plasminogen activator using human Tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108372((E)-3-(5-Chloro-2-guanidino-pyridin-3-yl)-acrylic ...)
Affinity DataKi:  2.79E+5nMAssay Description:Ability to inhibit human plasmin using Chromozym-PL as substrate at concentration of 1 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108370(CHEMBL53946 | N-(5-Chloro-3-phenoxy-pyridin-2-yl)-...)
Affinity DataKi:  3.42E+5nMAssay Description:Ability to inhibit tissue plasminogen activator (quadratech) and S-2444 as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed