Compile Data Set for Download or QSAR
maximum 50k data
Found 176 with Last Name = 'park' and Initial = 'hd'
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111121(2N-(4-Benzamidinemethyl)-1-[2-Cyclohexylaminosulfo...)
Affinity DataKi:  0.00300nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111110(2N-(4-Benzamidinemethyl)-1-[2-aminosulfonamido-3,3...)
Affinity DataKi:  0.00300nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111101((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.00300nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111101((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.00300nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111110(2N-(4-Benzamidinemethyl)-1-[2-aminosulfonamido-3,3...)
Affinity DataKi:  0.00300nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131789(1-(2-sulfonamide-amino-3,3-diphenyl-propionyl)-pyr...)
Affinity DataKi:  0.00400nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111105((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.00500nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111108(2N-(4-Benzamidinemethyl)-1-[2-Benzylsulfonamido-3,...)
Affinity DataKi:  0.00500nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111105((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.00500nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131790(1-(2-sulfonamideamino-3,3-diphenyl-propionyl)-pyrr...)
Affinity DataKi:  0.00800nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131778(3-(1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-2-...)
Affinity DataKi:  0.0100nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131795(1-(2-sulfonamideamino-3,3-diphenyl-propionyl)-pyrr...)
Affinity DataKi:  0.0100nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111120(2N-(4-Benzamidinemethyl)-1-[2-Aminoaceticacid-3,3-...)
Affinity DataKi:  0.0130nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131796((1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-2-yl...)
Affinity DataKi:  0.0150nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111120(2N-(4-Benzamidinemethyl)-1-[2-Aminoaceticacid-3,3-...)
Affinity DataKi:  0.0150nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131780((1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-2-yl...)
Affinity DataKi:  0.0150nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131791(1-(2-sulfonamideamino-3,3-diphenyl-propionyl)-pyrr...)
Affinity DataKi:  0.0150nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131792((1-Benzhydryl-2-{2-[(6-carbamimidoyl-pyridin-3-ylm...)
Affinity DataKi:  0.0170nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131798(1-(2-Methylamino-3,3-diphenyl-propionyl)-pyrrolidi...)
Affinity DataKi:  0.0200nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131782(1-(2-sulfonamide-amino-3,3-diphenyl-propionyl)-pyr...)
Affinity DataKi:  0.0200nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111102((S)-1-((R)-3-Cyclohexyl-2-methanesulfonylamino-pro...)
Affinity DataKi:  0.0200nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111122(2N-(4-Benzamidinemethyl)-1-[2-Carbamicacidmethyles...)
Affinity DataKi:  0.0300nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111104(2N-(4-Benzamidinemethyl)-1-[2-Amino-3,3-diphenyl-(...)
Affinity DataKi:  0.0360nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111122(2N-(4-Benzamidinemethyl)-1-[2-Carbamicacidmethyles...)
Affinity DataKi:  0.0360nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111109({(R)-1-Benzhydryl-2-[(S)-2-(4-carbamimidoyl-benzyl...)
Affinity DataKi:  0.0440nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111098(2N-(4-Benzamidinemethyl)-1-[2-Phenylamino-3,3-diph...)
Affinity DataKi:  0.0450nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111103((S)-1-[(R)-3-(3,4-Dichloro-phenyl)-2-methanesulfon...)
Affinity DataKi:  0.0500nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111118(2N-(4-Benzamidinemethyl)-1-[2-Hydroxysulfonamido-3...)
Affinity DataKi:  0.100nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131787((1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-3-yl...)
Affinity DataKi:  0.100nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131781(1-(2-sulfonamide-amino-3,3-diphenyl-propionyl)-pyr...)
Affinity DataKi:  0.120nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111114(2N-(4-Benzamidinemethyl)-1-[2-Acetylamino-3,3-diph...)
Affinity DataKi:  0.160nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131797(1-(2-sulfonamide-amino-3,3-diphenyl-propionyl)-pyr...)
Affinity DataKi:  0.160nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131779((1-Benzhydryl-2-{2-[(4-carbamimidoyl-thiophen-2-yl...)
Affinity DataKi:  0.170nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111121(2N-(4-Benzamidinemethyl)-1-[2-Cyclohexylaminosulfo...)
Affinity DataKi:  0.25nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111110(2N-(4-Benzamidinemethyl)-1-[2-aminosulfonamido-3,3...)
Affinity DataKi:  0.300nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1/Trypsin-2(Homo sapiens (Human))
Lg Life Sciences

Curated by ChEMBL
LigandPNGBDBM50131780((1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-2-yl...)
Affinity DataKi:  0.300nMAssay Description:In vitro inhibition constant (Ki) against human human trypsin was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111122(2N-(4-Benzamidinemethyl)-1-[2-Carbamicacidmethyles...)
Affinity DataKi:  0.310nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50069294((S)-3-[4-(carbohydrazonamidol)-phenyl]-N-cyclopent...)
Affinity DataKi:  0.380nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50069294((S)-3-[4-(carbohydrazonamidol)-phenyl]-N-cyclopent...)
Affinity DataKi:  0.380nMAssay Description:Binding affinity towards human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50069294((S)-3-[4-(carbohydrazonamidol)-phenyl]-N-cyclopent...)
Affinity DataKi:  0.380nMAssay Description:Compound was tested for inhibitory activity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131784(2-{4-[(Z)-amino(hydrazono)methyl]phenyl}-N-cyclope...)
Affinity DataKi:  0.400nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131783(1-(2-sulfonamide-amino-3,3-diphenyl-propionyl)-pyr...)
Affinity DataKi:  0.430nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111117((S)-1-((R)-2-Cyclohexyl-2-methanesulfonylamino-ace...)
Affinity DataKi:  0.5nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111099(2N-(5-carbohydrazonamide-2-thienylmethyl)-1-[2-met...)
Affinity DataKi:  0.530nMAssay Description:Binding affinity against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111108(2N-(4-Benzamidinemethyl)-1-[2-Benzylsulfonamido-3,...)
Affinity DataKi:  0.580nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111105((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.600nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131788((1-Benzhydryl-2-{2-[(5-carbamimidoyl-thiophen-3-yl...)
Affinity DataKi:  0.600nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50131793((1-Benzhydryl-2-{2-[(4-carbamimidoyl-thiazol-2-ylm...)
Affinity DataKi:  0.640nMAssay Description:In vitro inhibition constant (Ki) against human thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111101((S)-1-((R)-2-Methanesulfonylamino-3,3-diphenyl-pro...)
Affinity DataKi:  0.700nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bos taurus (bovine))
Life Science R & D, Lgci

Curated by ChEMBL
LigandPNGBDBM50111103((S)-1-[(R)-3-(3,4-Dichloro-phenyl)-2-methanesulfon...)
Affinity DataKi:  0.800nMAssay Description:Binding affinity against bovine trypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 176 total ) | Next | Last >>
Jump to: