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Found 17 Enz. Inhib. hit(s) with all data for entry = 50018255
LigandPNGBDBM50110681(CHEMBL430266 | Calyculin-A)
Affinity DataIC50:  0.25nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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LigandPNGBDBM50408820(CHEMBL5268133)
Affinity DataIC50:  1nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50110690(CHEMBL17377 | FOSTRIECIN | Phosphoric acid mono-{3...)
Affinity DataIC50: >1nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50061067(15-(3-Guanidino-propyl)-8-isobutyl-18-((1E,3E)-6-m...)
Affinity DataIC50:  1nMAssay Description:Antagonist activity at NK2 receptor in human urinary bladder assessed as inhibition of [beta-Ala8]NKA(4-10)-induced tissue contractionsMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50110681(CHEMBL430266 | Calyculin-A)
Affinity DataIC50:  3nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50408820(CHEMBL5268133)
Affinity DataIC50:  3.5nMAssay Description:Antagonist activity at mouse histamine H4 receptor in SK-N-MC cells assessed as inhibition of forskolin-stimulated cAMP release preincubated for 10 m...More data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50408822(CHEMBL5276260)
Affinity DataIC50:  4nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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LigandPNGBDBM50090505((1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2...)
Affinity DataIC50:  8nMAssay Description:Antagonist activity at mouse histamine H4 receptor in SK-N-MC cells assessed as inhibition of forskolin-stimulated cAMP release preincubated for 10 m...More data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50366883(TAUTOMYCIN)
Affinity DataIC50:  10nMAssay Description:Antagonist activity at mouse histamine H4 receptor in SK-N-MC cells assessed as inhibition of forskolin-stimulated cAMP release preincubated for 10 m...More data for this Ligand-Target Pair
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LigandPNGBDBM50110681(CHEMBL430266 | Calyculin-A)
Affinity DataIC50:  10nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50408823(CHEMBL5276593)
Affinity DataIC50:  12nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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LigandPNGBDBM50090505((1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2...)
Affinity DataIC50:  160nMAssay Description:Antagonist activity at rat H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after 6 hrsMore data for this Ligand-Target Pair
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LigandPNGBDBM50408821(CHEMBL5270968)
Affinity DataIC50:  400nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50090505((1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2...)
Affinity DataIC50:  400nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50090505((1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2...)
Affinity DataIC50:  600nMAssay Description:Antagonist activity at rat H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after 6 hrsMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM22319((5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoic acid | ...)
Affinity DataEC50:  7.80nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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TargetSerine/threonine-protein phosphatase 5(Homo sapiens (Human))TBA
LigandPNGBDBM50408824(CHAULMOOGRIC ACID | CHEBI:61391 | Chaulmoogric Aci...)
Affinity DataEC50:  1.30nMAssay Description:Inhibition of human H-PGDS expressed in Escherichia coli BL21 DE2 by enzyme immuno assay at 50 uMMore data for this Ligand-Target Pair
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