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Assay Detail

CHEMBL906678

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Functional
Inhibition of serum-induced proliferation of human A375 cells
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A-375
Confidence 1 — Organism
Curated By Autocuration

Target

A-375 (CHEMBL613859)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and biological evaluation of sulfonylhydrazone-substituted imidazo[1,2-a]pyridines as novel PI3 kinase p110alpha inhibitors.
Hayakawa M, Kawaguchi K, Kaizawa H, Koizumi T, Ohishi T, Yamano M, Okada M, Ohta M, Tsukamoto S, Raynaud FI, Parker P, Workman P, Waterfield MD.
Bioorg Med Chem (2007) 15 : 5837 -5844
PubMed 17601739 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.95 7.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL555968 1 7.48
CHEMBL536070 1 7.25
CHEMBL556399 1 7.24
CHEMBL541642 1 7.05
CHEMBL559361 1 6.92
CHEMBL535170 1 6.75
CHEMBL224769 1 6.14
CHEMBL98350 LY-294002 -1.0 1 5.08
CHEMBL229097 1 5.05
CHEMBL558174 1 5.05
CHEMBL535171 1 5.03
CHEMBL229046 1 4.92
CHEMBL229098 1 4.70
CHEMBL427066 1 4.64
CHEMBL387636 1 -
CHEMBL389843 1 -
CHEMBL53463 DOXORUBICIN 4.0 1 -
CHEMBL428647 PACLITAXEL 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL555968 IC50 = 33.0 nM 7.48
CHEMBL536070 IC50 = 56.0 nM 7.25
CHEMBL556399 IC50 = 58.0 nM 7.24
CHEMBL541642 IC50 = 90.0 nM 7.05
CHEMBL559361 IC50 = 120.0 nM 6.92
CHEMBL535170 IC50 = 180.0 nM 6.75
CHEMBL224769 IC50 = 730.0 nM 6.14
CHEMBL98350 LY-294002 IC50 = 8400.0 nM 5.08
CHEMBL229097 IC50 = 9000.0 nM 5.05
CHEMBL558174 IC50 = 8960.0 nM 5.05
CHEMBL535171 IC50 = 9350.0 nM 5.03
CHEMBL229046 IC50 = 12000.0 nM 4.92
CHEMBL229098 IC50 = 20000.0 nM 4.70
CHEMBL427066 IC50 = 23000.0 nM 4.64
CHEMBL387636 IC50 - -
CHEMBL389843 IC50 - -
CHEMBL53463 DOXORUBICIN IC50 - -
CHEMBL428647 PACLITAXEL IC50 - -