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Assay Detail

CHEMBL1646729

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Binding
Inhibition of human PI3K p110delta catalytic subunit by AlphaScreen assay
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Discovery of novel class 1 phosphatidylinositide 3-kinases (PI3K) fragment inhibitors through structure-based virtual screening.
Giordanetto F, Kull B, Dellsén A.
Bioorg Med Chem Lett (2011) 21 : 829 -835
PubMed 21169017 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 5.10 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL428496 WORTMANNIN 1 8.40
CHEMBL1645106 1 5.29
CHEMBL1645108 1 5.19
CHEMBL1645100 1 5.19
CHEMBL1645110 1 5.17
CHEMBL1645107 1 5.05
CHEMBL1645095 1 4.96
CHEMBL1645101 1 4.92
CHEMBL1645102 1 4.75
CHEMBL1645103 1 4.43
CHEMBL1645094 1 4.39
CHEMBL1645098 1 4.37
CHEMBL58782 1 4.18
CHEMBL1645099 1 -
CHEMBL1645104 1 -
CHEMBL1645105 1 -
CHEMBL1645097 1 -
CHEMBL1645096 1 -
CHEMBL1645109 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL428496 WORTMANNIN IC50 = 4.0 nM 8.40
CHEMBL1645106 IC50 = 5100.0 nM 5.29
CHEMBL1645108 IC50 = 6500.0 nM 5.19
CHEMBL1645100 IC50 = 6400.0 nM 5.19
CHEMBL1645110 IC50 = 6800.0 nM 5.17
CHEMBL1645107 IC50 = 8900.0 nM 5.05
CHEMBL1645095 IC50 = 11100.0 nM 4.96
CHEMBL1645101 IC50 = 12000.0 nM 4.92
CHEMBL1645102 IC50 = 18000.0 nM 4.75
CHEMBL1645103 IC50 = 36800.0 nM 4.43
CHEMBL1645094 IC50 = 40800.0 nM 4.39
CHEMBL1645098 IC50 = 43000.0 nM 4.37
CHEMBL58782 IC50 = 65700.0 nM 4.18
CHEMBL1645099 IC50 > 83300.0 nM -
CHEMBL1645104 IC50 - -
CHEMBL1645105 IC50 - -
CHEMBL1645097 IC50 - -
CHEMBL1645096 IC50 > 83300.0 nM -
CHEMBL1645109 IC50 - -