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Assay Detail

CHEMBL887587

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Functional
Antiproliferative activity against A375 cells
10
Total Activities
10
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 pyrido[3',2':4,5]furo[3,2-d]pyrimidine derivatives as novel PI3 kinase p110alpha inhibitors.
Hayakawa M, Kaizawa H, Moritomo H, Koizumi T, Ohishi T, Yamano M, Okada M, Ohta M, Tsukamoto S, Raynaud FI, Workman P, Waterfield MD, Parker P.
Bioorg Med Chem Lett (2007) 17 : 2438 -2442
PubMed 17339109 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 5.26 6.48

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL538346 1 6.48
CHEMBL3216649 1 5.41
CHEMBL3216005 1 5.01
CHEMBL3215760 1 4.93
CHEMBL3216006 1 4.91
CHEMBL537877 1 4.80
CHEMBL388480 1 -
CHEMBL534951 1 -
CHEMBL541906 1 -
CHEMBL390623 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL538346 IC50 = 330.0 nM 6.48
CHEMBL3216649 IC50 = 3870.0 nM 5.41
CHEMBL3216005 IC50 = 9670.0 nM 5.01
CHEMBL3215760 IC50 = 11760.0 nM 4.93
CHEMBL3216006 IC50 = 12320.0 nM 4.91
CHEMBL537877 IC50 = 15780.0 nM 4.80
CHEMBL388480 IC50 - -
CHEMBL534951 IC50 > 30000.0 nM -
CHEMBL541906 IC50 > 30000.0 nM -
CHEMBL390623 IC50 > 30000.0 nM -