Compile Data Set for Download or QSAR
maximum 50k data
Found 9 Enz. Inhib. hit(s) with all data for entry = 50011908
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111969(CHEMBL440638 | T140 analogue)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibitory activity of the compound was determined based on theinhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXCR...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111973(CHEMBL440998 | cyclic pseudopeptide Analogue)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibitory activity of the compound was determined based on theinhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXCR...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111971(CHEMBL409991 | cyclic pseudopeptide Analogue)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibitory activity of the compound was determined based on theinhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXCR...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111971(CHEMBL409991 | cyclic pseudopeptide Analogue)
Affinity DataIC50:  7.30E+3nMAssay Description:Inhibitory activity of the compound was determined based on theinhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXCR...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111969(CHEMBL440638 | T140 analogue)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibitory activity of the compound was determined based on the inhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXC...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111970(CHEMBL414085 | Pseudopeptide Analogue)
Affinity DataIC50:  2.70E+4nMAssay Description:Inhibitory activity of the compound was determined based on the inhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through C-X...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111970(CHEMBL414085 | Pseudopeptide Analogue)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibitory activity of the compound was determined based on theinhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through C-X-...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111972(CHEMBL266632 | T140 analogue)
Affinity DataIC50:  3.60E+4nMAssay Description:Inhibitory activity of the compound was determined based on the inhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXC...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetC-X-C chemokine receptor type 4(Homo sapiens (Human))
Kyoto University

Curated by ChEMBL
LigandPNGBDBM50111968(CHEMBL439700 | T140 analogue)
Affinity DataIC50:  1.70E+5nMAssay Description:Inhibitory activity of the compound was determined based on the inhibition of [Ca2+] mobilization induced by human SDF-1alpha stimulation through CXC...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed