Compile Data Set for Download or QSAR
Report error Found 137 Enz. Inhib. hit(s) with all data for entry = 50011665
LigandPNGBDBM50549829(CHEMBL4760520)
Affinity DataIC50: 100nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549828(CHEMBL4795990)
Affinity DataIC50: 130nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549837(CHEMBL4759283)
Affinity DataIC50: 180nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549855(CHEMBL4756664)
Affinity DataIC50: 200nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549833(CHEMBL4749552)
Affinity DataIC50: 230nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549845(CHEMBL4764065)
Affinity DataIC50: 290nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549853(CHEMBL4744017)
Affinity DataIC50: 310nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549843(CHEMBL4787005)
Affinity DataIC50: 330nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549835(CHEMBL4779628)
Affinity DataIC50: 340nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549854(CHEMBL4784202)
Affinity DataIC50: 380nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549838(CHEMBL4762194)
Affinity DataIC50: 410nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549856(CHEMBL4761824)
Affinity DataIC50: 430nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549840(CHEMBL4800674)
Affinity DataIC50: 490nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549847(CHEMBL4761358)
Affinity DataIC50: 490nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2C9(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549828(CHEMBL4795990)
Affinity DataIC50: 490nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549836(CHEMBL4787554)
Affinity DataIC50: 510nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549832(CHEMBL4757894)
Affinity DataIC50: 560nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549846(CHEMBL4764646)
Affinity DataIC50: 600nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549834(CHEMBL4753474)
Affinity DataIC50: 640nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
LigandPNGBDBM50549831(CHEMBL4740213)
Affinity DataIC50: 760nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549849(CHEMBL4789398)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549857(CHEMBL4749369)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549842(CHEMBL4764754)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549852(CHEMBL4749625)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549844(CHEMBL4749950)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2C9(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549837(CHEMBL4759283)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549830(CHEMBL4797330)
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549848(CHEMBL4749807)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PI3Kgamma in human THP-1 cells assessed as reduction in Akt phosphorylation at Ser473 residueMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2C9(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549846(CHEMBL4764646)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2C9(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549854(CHEMBL4784202)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549828(CHEMBL4795990)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of human ERG by planar patch clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCytochrome P450 2C9(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549855(CHEMBL4756664)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549854(CHEMBL4784202)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of human ERG by planar patch clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549837(CHEMBL4759283)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by planar patch clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549846(CHEMBL4764646)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by planar patch clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Vertex Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50549855(CHEMBL4756664)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG by planar patch clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549829(CHEMBL4760520)
Affinity DataKi:  3nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549837(CHEMBL4759283)
Affinity DataKi:  3nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549855(CHEMBL4756664)
Affinity DataKi:  3nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549828(CHEMBL4795990)
Affinity DataKi:  4nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549854(CHEMBL4784202)
Affinity DataKi:  4nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549856(CHEMBL4761824)
Affinity DataKi:  4nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549843(CHEMBL4787005)
Affinity DataKi:  5nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549833(CHEMBL4749552)
Affinity DataKi:  6nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549838(CHEMBL4762194)
Affinity DataKi:  6nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549840(CHEMBL4800674)
Affinity DataKi:  6nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549845(CHEMBL4764065)
Affinity DataKi:  6nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549835(CHEMBL4779628)
Affinity DataKi:  7nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM50549834(CHEMBL4753474)
Affinity DataKi:  9nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
LigandPNGBDBM50549853(CHEMBL4744017)
Affinity DataKi:  9nMAssay Description:Inhibition of PI3Kgamma (unknown origin) using PIP2 as substrate measured after 15 mins in presence of [33P]-ATP by liquid scintillation counting met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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