Compile Data Set for Download or QSAR
Report error Found 23 Enz. Inhib. hit(s) with all data for entry = 50022402
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651837(CHEMBL5639851)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kgamma (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651838(CHEMBL5647196)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651837(CHEMBL5639851)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kdelta (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651838(CHEMBL5647196)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kbeta (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651838(CHEMBL5647196)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kgamma (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651837(CHEMBL5639851)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kbeta (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651838(CHEMBL5647196)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kalpha (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50651837(CHEMBL5639851)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of PI3Kalpha (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetHigh affinity nerve growth factor receptor(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50524980(CHEMBL4437605)
Affinity DataIC50: 2.5nMAssay Description:Inhibition of TRKA (unknown origin) by Ambit kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50604450(CHEMBL5180040)
Affinity DataIC50: 3nMAssay Description:Inhibition of RET (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetAP2-associated protein kinase 1(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50502295(CHEMBL4439128)
Affinity DataIC50: 4nMAssay Description:Inhibition of AAK1 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50524980(CHEMBL4437605)
Affinity DataIC50: 23nMAssay Description:Inhibition of ALK (unknown origin) by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50623376(CHEMBL5412018)
Affinity DataIC50: 30nMAssay Description:Inhibition of PDK1 (unknown origin) incubated for 30 mins followed by substrate addition measured after 60 mins in presence of ATP by ADP-Glo lumines...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50623380(CHEMBL5411651)
Affinity DataIC50: 30nMAssay Description:Inhibition of PDK1 (unknown origin) incubated for 30 mins followed by substrate addition measured after 60 mins in presence of ATP by ADP-Glo lumines...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50623379(CHEMBL5396356)
Affinity DataIC50: 30nMAssay Description:Inhibition of PDK1 (unknown origin) incubated for 30 mins followed by substrate addition measured after 60 mins in presence of ATP by ADP-Glo lumines...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50623378(CHEMBL5436815)
Affinity DataIC50: 30nMAssay Description:Inhibition of PDK1 (unknown origin) incubated for 30 mins followed by substrate addition measured after 60 mins in presence of ATP by ADP-Glo lumines...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
Target[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50623377(CHEMBL5438177)
Affinity DataIC50: 30nMAssay Description:Inhibition of PDK1 (unknown origin) incubated for 30 mins followed by substrate addition measured after 60 mins in presence of ATP by ADP-Glo lumines...More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50604450(CHEMBL5180040)
Affinity DataIC50: 50nMAssay Description:Inhibition of RET (unknown origin) by DiscoverX KINOMEscan assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50633440(CHEMBL5427291)
Affinity DataIC50: 80nMAssay Description:Inhibition of human RIPK1 by ADP-Glo assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50633440(CHEMBL5427291)
Affinity DataIC50: 88nMAssay Description:Inhibition of RIPK1 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50633421(CHEMBL5416808)
Affinity DataIC50: 90nMAssay Description:Inhibition of RIPK1 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 1(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50633410(CHEMBL5407487)
Affinity DataIC50: 1.47E+3nMAssay Description:Inhibition of RIPK1 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed
TargetReceptor-interacting serine/threonine-protein kinase 3(Human)
Hunan University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50633440(CHEMBL5427291)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of RIPK3 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2025
Entry Details
PubMed