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Assay Detail

CHEMBL3592210

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Functional
Cytotoxic activity against human SKOV3 cells expressing PIK3CA mutant incubated for 72 hrs by SRB assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type SK-OV-3
Confidence 1 — Organism
Curated By Autocuration

Target

SK-OV-3 (CHEMBL614925)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of novel condensed pyrrolo[1,2-c]pyrimidines featuring morpholine moiety as PI3Kα inhibitors.
Ibrahim MA, Abou-Seri SM, Hanna MM, Abdalla MM, El Sayed NA.
Eur J Med Chem (2015) 99 : 1 -13
PubMed 26037808 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 4.92 5.87

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3589372 1 5.87
CHEMBL3589370 1 5.78
CHEMBL3589371 1 5.45
CHEMBL3589324 1 5.33
CHEMBL3589377 1 5.24
CHEMBL3589379 1 5.18
CHEMBL3589376 1 5.12
CHEMBL3589378 1 4.91
CHEMBL3589375 1 4.84
CHEMBL3589320 1 4.69
CHEMBL3589321 1 4.66
CHEMBL3589323 1 4.23
CHEMBL3589322 1 4.22
CHEMBL3589373 1 4.13
CHEMBL3589374 1 4.11

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3589372 IC50 = 1340.0 nM 5.87
CHEMBL3589370 IC50 = 1670.0 nM 5.78
CHEMBL3589371 IC50 = 3560.0 nM 5.45
CHEMBL3589324 IC50 = 4670.0 nM 5.33
CHEMBL3589377 IC50 = 5780.0 nM 5.24
CHEMBL3589379 IC50 = 6540.0 nM 5.18
CHEMBL3589376 IC50 = 7650.0 nM 5.12
CHEMBL3589378 IC50 = 12340.0 nM 4.91
CHEMBL3589375 IC50 = 14560.0 nM 4.84
CHEMBL3589320 IC50 = 20540.0 nM 4.69
CHEMBL3589321 IC50 = 21670.0 nM 4.66
CHEMBL3589323 IC50 = 58530.0 nM 4.23
CHEMBL3589322 IC50 = 60460.0 nM 4.22
CHEMBL3589373 IC50 = 74530.0 nM 4.13
CHEMBL3589374 IC50 = 78450.0 nM 4.11