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Assay Detail

CHEMBL5654102

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Binding
Inhibition of p110 delta (unknown origin)
10
Total Activities
10
Compounds Tested
1
Activity Types
2
Assay Parameters

Assay Information

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

Publication

ZSTK474, a novel phosphatidylinositol 3-kinase inhibitor identified using the JFCR39 drug discovery system.
Kong DX, Yamori T.
Acta Pharmacol Sin (2010) 31 : 1189 -1197
PubMed 20729870 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 7.88 9.00

Assay Parameters

Parameter Type Value Units Text
EFO_ID EFO_ID - MONDO:0004992
EFO_TERM EFO_TERM - cancer

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1236962 OMIPALISIB 2.0 1 9.00
CHEMBL411907 SONOLISIB 2.0 1 8.52
CHEMBL521851 PICTILISIB 2.0 1 8.52
CHEMBL1879463 DACTOLISIB 3.0 1 8.30
CHEMBL586702 ZSTK-474 2.0 1 8.30
CHEMBL1922094 APITOLISIB 2.0 1 8.15
CHEMBL3360203 PILARALISIB 2.0 1 7.44
CHEMBL3349370 1 7.37
CHEMBL2017974 BUPARLISIB 3.0 1 6.94
CHEMBL1213082 1 6.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1236962 OMIPALISIB IC50 = 1.0 nM 9.00
CHEMBL411907 SONOLISIB IC50 = 3.0 nM 8.52
CHEMBL521851 PICTILISIB IC50 = 3.0 nM 8.52
CHEMBL1879463 DACTOLISIB IC50 = 5.0 nM 8.30
CHEMBL586702 ZSTK-474 IC50 = 5.0 nM 8.30
CHEMBL1922094 APITOLISIB IC50 = 7.0 nM 8.15
CHEMBL3360203 PILARALISIB IC50 = 36.0 nM 7.44
CHEMBL3349370 IC50 = 43.0 nM 7.37
CHEMBL2017974 BUPARLISIB IC50 = 116.0 nM 6.94
CHEMBL1213082 IC50 = 500.0 nM 6.30