Compile Data Set for Download or QSAR
Found 375 with Last Name = 'garlich' and Initial = 'jr'
TargetBromodomain-containing protein 4 [368-440](Homo sapiens (Human))
SignalRx Pharmaceuticals, Inc.

US Patent
LigandPNGBDBM259884(US10308662, Compound 125 | US9505780, 125)copy SMILEScopy InChI
Affinity DataIC50: 1.87nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50403068(CHEMBL2216870 | IDELALISIB | US9745321, CAL-101)copy SMILEScopy InChI
Affinity DataIC50: 2.5nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427456(CHEMBL2326953 | US10308662, Compound 44 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427456(CHEMBL2326953 | US10308662, Compound 44 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427456(CHEMBL2326953 | US10308662, Compound 44 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427485(CHEMBL2326959 | US10308662, Compound 120 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427455(CHEMBL2326951)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427489(CHEMBL2326955)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427485(CHEMBL2326959 | US10308662, Compound 120 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427485(CHEMBL2326959 | US10308662, Compound 120 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427459(CHEMBL2326954)copy SMILEScopy InChI
Affinity DataIC50: 26nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427457(CHEMBL2326952 | US10308662, Compound 25 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427457(CHEMBL2326952 | US10308662, Compound 25 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427457(CHEMBL2326952 | US10308662, Compound 25 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetBromodomain-containing protein 4 [75-147](Homo sapiens (Human))
SignalRx Pharmaceuticals, Inc.

US Patent
LigandPNGBDBM259897(US9505780, JQ-1)copy SMILEScopy InChI
Affinity DataIC50: 27.1nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetBromodomain-containing protein 4 [44-167](Homo sapiens (Human))
Pfizer

LigandPNGBDBM50365262((+)-JQ1 | (S)-JQ1 (1) | CHEMBL1957266 | JQ1 | US10...)copy SMILEScopy InChI
Affinity DataIC50: 27.1nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427453(CHEMBL2322228 | US10308662, Compound 28 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427453(CHEMBL2322228 | US10308662, Compound 28 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
LigandPNGBDBM50427453(CHEMBL2322228 | US10308662, Compound 28 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 34nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetBromodomain-containing protein 4 [368-440](Homo sapiens (Human))
SignalRx Pharmaceuticals, Inc.

US Patent
LigandPNGBDBM259897(US9505780, JQ-1)copy SMILEScopy InChI
Affinity DataIC50: 39.1nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetBromodomain-containing protein 4 [349-460](Homo sapiens (Human))
Pfizer

LigandPNGBDBM50365262((+)-JQ1 | (S)-JQ1 (1) | CHEMBL1957266 | JQ1 | US10...)copy SMILEScopy InChI
Affinity DataIC50: 39.1nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetSerine/threonine-protein kinase pim-1(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427453(CHEMBL2322228 | US10308662, Compound 28 | US950578...)copy SMILEScopy InChI
Affinity DataIC50: 43nMAssay Description:Inhibition of PIM1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427489(CHEMBL2326955)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM259879(US10308662, Compound 118 | US9505780, 118)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM259879(US10308662, Compound 118 | US9505780, 118)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
LigandPNGBDBM50427488(CHEMBL2326956 | US10308662, Compound 100 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 55.2nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427488(CHEMBL2326956 | US10308662, Compound 100 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 55.2nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427459(CHEMBL2326954)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427492(CHEMBL2322244)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427480(CHEMBL2326964)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427481(CHEMBL2326963)copy SMILEScopy InChI
Affinity DataIC50: 71nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427467(CHEMBL2322229)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427493(CHEMBL2322243)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427475(CHEMBL2326967)copy SMILEScopy InChI
Affinity DataIC50: 77nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427488(CHEMBL2326956 | US10308662, Compound 100 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427460(CHEMBL2322236)copy SMILEScopy InChI
Affinity DataIC50: 85nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427482(CHEMBL2326962)copy SMILEScopy InChI
Affinity DataIC50: 86nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50403068(CHEMBL2216870 | IDELALISIB | US9745321, CAL-101)copy SMILEScopy InChI
Affinity DataIC50: 89nMAssay Description:Inhibition of PI3K p110gamma (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
LigandPNGBDBM259879(US10308662, Compound 118 | US9505780, 118)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM259879(US10308662, Compound 118 | US9505780, 118)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
LigandPNGBDBM50427485(CHEMBL2326959 | US10308662, Compound 120 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 95nMAssay Description:Inhibitory activity can be determined routinely using known methods and also from commercial vendors offering this service for kinases and bromodomai...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q24170D7US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427491(CHEMBL2322245)copy SMILEScopy InChI
Affinity DataIC50: 95nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427485(CHEMBL2326959 | US10308662, Compound 120 | US95057...)copy SMILEScopy InChI
Affinity DataIC50: 95nMAssay Description:Several TP Scaffold compounds were tested for inhibition activity against isoforms of PI3K (alpha, beta, gamma, and delta isoforms) and the bromodoma...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22B8WZ1US Patent
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427463(CHEMBL2322233)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427484(CHEMBL2326960)copy SMILEScopy InChI
Affinity DataIC50: 109nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427469(CHEMBL2322226)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427464(CHEMBL2322232)copy SMILEScopy InChI
Affinity DataIC50: 112nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427471(CHEMBL2326971)copy SMILEScopy InChI
Affinity DataIC50: 116nMAssay Description:Inhibition of PI3K p110alpha (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427460(CHEMBL2322236)copy SMILEScopy InChI
Affinity DataIC50: 125nMAssay Description:Inhibition of PI3K p110delta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform(Homo sapiens (Human))
The University of Arizona

Curated by ChEMBL
LigandPNGBDBM50427477(CHEMBL2322242)copy SMILEScopy InChI
Affinity DataIC50: 134nMAssay Description:Inhibition of PI3K p110beta (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89DR9PubMed
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