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Found 52 Enz. Inhib. hit(s) with Target = 'Integrin beta'
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324824((S)-2-(2-(benzofuran-2-carbonyl)-5,7-dichloro-1,2,...)
Affinity DataIC50:  5nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324822((S)-2-(2-(benzofuran-6-carbonyl)-5,7-dichloro-1,2,...)
Affinity DataIC50:  9nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324810((S)-2-(5,7-dichloro-2-(4-methylbenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  10nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324823((S)-2-(5,7-dichloro-2-(2,3-dihydrobenzofuran-6-car...)
Affinity DataIC50:  13nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Mus musculus)
University Of Bradford

Curated by ChEMBL
LigandPNGBDBM50083811(3-({1-[3-(1H-Imidazol-2-ylamino)-propyl]-1H-indazo...)
Affinity DataIC50:  21nMAssay Description:Antagonist activity at mouse endothelial alpha2bbeta3 integrin receptor by cell adhesion assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324812((S)-2-(5,7-dichloro-2-(4-chlorobenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  22nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324806((S,E)-2-(5,7-dichloro-2-(3-(furan-2-yl)acryloyl)-1...)
Affinity DataIC50:  25nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324816((S)-3-benzamido-2-(5,7-dichloro-2-(4-chlorobenzoyl...)
Affinity DataIC50:  29nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-8(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50199345(CHEMBL3893700 | US10131658, Compound 201)
Affinity DataIC50:  40nMAssay Description:Inhibition of human integrin alphaVbeta8-mediated human SNB19 cell adhesion to recombinant human TGFbeta1 LAP preincubated for 15 to 30 mins followed...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50092956(1-(4-Acetyl-piperazin-1-yl)-3-[4-(2-isopropyl-phen...)
Affinity DataIC50:  44nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324817((S)-2-(5,7-dichloro-2-(4-chlorobenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  51nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324811((S)-2-(5,7-dichloro-2-(3-chlorobenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  66nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324807((S)-2-(2-benzoyl-5,7-dichloro-1,2,3,4-tetrahydrois...)
Affinity DataIC50:  79nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324809((S)-2-(5,7-dichloro-2-(3-methylbenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  90nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50004058((2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-yl...)
Affinity DataIC50:  130nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50004058((2S)-2-(butylsulfonylamino)-3-[4-(4-piperidin-4-yl...)
Affinity DataIC50:  136nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
TargetIntegrin beta-8(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50199196(CHEMBL3905970)
Affinity DataIC50:  400nMAssay Description:Inhibition of human integrin alphaVbeta8-mediated human SNB19 cell adhesion to recombinant human TGFbeta1 LAP preincubated for 15 to 30 mins followed...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324808((S)-2-(5,7-dichloro-2-(2-methylbenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  460nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324815((S)-3-(cyclohexanecarboxamido)-2-(5,7-dichloro-2-(...)
Affinity DataIC50:  540nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50568659(CHEMBL4861415)
Affinity DataIC50:  603nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50568659(CHEMBL4861415)
Affinity DataIC50:  610nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324814((S)-3-acetamido-2-(5,7-dichloro-2-(4-chlorobenzoyl...)
Affinity DataIC50:  620nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324819((S)-2-(5,7-dichloro-2-(4-chlorobenzoyl)-1,2,3,4-te...)
Affinity DataIC50:  810nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50568658(CHEMBL4853717)
Affinity DataIC50:  890nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-3(Rattus norvegicus)
University Of Hawai'I At Hilo

Curated by ChEMBL
LigandPNGBDBM50568658(CHEMBL4853717)
Affinity DataIC50:  897nMAssay Description:Inhibition of fibrinogen binding to rat platelet integrin alpha2b beta3 by ELISA based solid phase binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324820((S)-2-(2-acetyl-5,7-dichloro-1,2,3,4-tetrahydroiso...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324818((S)-2-(5,7-dichloro-2-(4-chlorobenzoyl)-1,2,3,4-te...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324813((S)-3-amino-2-(5,7-dichloro-2-(4-chlorobenzoyl)-1,...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-2/Intercellular adhesion molecule 1(Homo sapiens (Human))
Sunesis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50324821((S)-2-(5,7-dichloro-2-(cyclohexanecarbonyl)-1,2,3,...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of LFA1/ICAM1 interaction in human Hut-78 cells by cell migration assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-8(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50199398(CHEMBL3952235 | US10131658, Compound 211)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human integrin alphaVbeta8-mediated human SNB19 cell adhesion to recombinant human TGFbeta1 LAP preincubated for 15 to 30 mins followed...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-8(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50199399(CHEMBL3909977 | US10131658, Compound 212)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human integrin alphaVbeta8-mediated human SNB19 cell adhesion to recombinant human TGFbeta1 LAP preincubated for 15 to 30 mins followed...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-8(Homo sapiens (Human))
University Of California San Francisco

Curated by ChEMBL
LigandPNGBDBM50199197(CHEMBL3923968 | US10131658, Compound 11)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human integrin alphaVbeta8-mediated human SNB19 cell adhesion to recombinant human TGFbeta1 LAP preincubated for 15 to 30 mins followed...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498778(CHEMBL3623207)
Affinity DataIC50:  2.48E+4nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498783(CHEMBL3623202)
Affinity DataIC50:  8.65E+4nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498781(CHEMBL3623205)
Affinity DataIC50:  9.31E+4nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498779(CHEMBL3623201)
Affinity DataIC50:  9.44E+4nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498777(CHEMBL3623200)
Affinity DataIC50:  9.61E+4nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498773(CHEMBL3623206)
Affinity DataIC50:  1.08E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498778(CHEMBL3623207)
Affinity DataIC50:  1.24E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of thrombin-induced platelet aggregation pr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-7(Homo sapiens (Human))
Technische UniversitäT MüNchen

Curated by ChEMBL
LigandPNGBDBM50070619((S)-N-((1S,2R)-1-Carbamoyl-2-hydroxy-propyl)-3-{(S...)
Affinity DataIC50:  2.80E+5nMAssay Description:Inhibition of alpha4-beta7 interaction to mucosal addressin cell adhesion molecule-1 (MAdCAM-1) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta-7(Homo sapiens (Human))
Technische UniversitäT MüNchen

Curated by ChEMBL
LigandPNGBDBM50137078(2-[4-benzyloxy-1-isobutoxymethyl-5a,9a-dimethoxy-(...)
Affinity DataIC50:  4.20E+5nMAssay Description:Inhibition of alpha4-beta7 interaction to mucosal addressin cell adhesion molecule-1 (MAdCAM-1) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498782(CHEMBL3623204)
Affinity DataIC50:  4.25E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498780(CHEMBL3623199)
Affinity DataIC50:  4.88E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498775(CHEMBL3622610)
Affinity DataIC50: >5.00E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498774(CHEMBL3623203)
Affinity DataIC50: >5.00E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498776(CHEMBL3623198)
Affinity DataIC50: >5.00E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498784(CHEMBL3623193)
Affinity DataIC50: >5.00E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of ADP-induced platelet aggregation preincu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498778(CHEMBL3623207)
Affinity DataIC50:  5.90E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of U46619-induced platelet aggregation prei...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta(Oryctolagus cuniculus)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50498778(CHEMBL3623207)
Affinity DataIC50:  6.83E+5nMAssay Description:Antagonist activity at GP2b/3a receptor in New Zealand rabbit platelet-rich plasma assessed as inhibition of collagen-induced platelet aggregation pr...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIntegrin beta-1(Homo sapiens (Human))
Technische UniversitäT MüNchen

Curated by ChEMBL
LigandPNGBDBM50137079((S)-17-Amino-11-((S)-sec-butyl)-14-(2-carbamoyl-et...)
Affinity DataIC50:  1.44E+6nMAssay Description:Inhibition of alpha4-beta1 interaction to vascular cell adhesion molecule-1 (VCAM-1) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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