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Assay Detail

CHEMBL4307007

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

Functional
Cytotoxicity against human OVCAR8 cells assessed as reduction in cell viability incubated for 72 hrs by SRB assay
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type OVCAR-8
Confidence 1 — Organism
Curated By Autocuration

Target

OVCAR-8 (CHEMBL612555)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of pyrazole-thiophene derivatives as highly Potent, orally active Akt inhibitors.
Zhan W, Che J, Xu L, Wu Y, Hu X, Zhou Y, Cheng G, Hu Y, Dong X, Li J.
Eur J Med Chem (2019) 180 : 72 -85
PubMed 31301565 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.73 6.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4435124 1 6.64
CHEMBL3137336 UPROSERTIB 2.0 1 6.27
CHEMBL4545734 1 6.24
CHEMBL4460688 1 6.19
CHEMBL4438248 1 5.86
CHEMBL4454791 1 5.83
CHEMBL4445702 1 5.80
CHEMBL4579551 1 5.76
CHEMBL4526242 1 5.60
CHEMBL4554198 1 5.57
CHEMBL4467970 1 5.50
CHEMBL4442226 1 5.25
CHEMBL4455194 1 5.14
CHEMBL4577134 1 4.55
CHEMBL4461200 1 -
CHEMBL4444441 1 -
CHEMBL2219422 AFURESERTIB 3.0 1 -
CHEMBL4451854 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4435124 IC50 = 230.0 nM 6.64
CHEMBL3137336 UPROSERTIB IC50 = 540.0 nM 6.27
CHEMBL4545734 IC50 = 580.0 nM 6.24
CHEMBL4460688 IC50 = 640.0 nM 6.19
CHEMBL4438248 IC50 = 1390.0 nM 5.86
CHEMBL4454791 IC50 = 1470.0 nM 5.83
CHEMBL4445702 IC50 = 1590.0 nM 5.80
CHEMBL4579551 IC50 = 1740.0 nM 5.76
CHEMBL4526242 IC50 = 2510.0 nM 5.60
CHEMBL4554198 IC50 = 2700.0 nM 5.57
CHEMBL4467970 IC50 = 3190.0 nM 5.50
CHEMBL4442226 IC50 = 5690.0 nM 5.25
CHEMBL4455194 IC50 = 7170.0 nM 5.14
CHEMBL4577134 IC50 = 27990.0 nM 4.55
CHEMBL4461200 IC50 > 50000.0 nM -
CHEMBL4444441 IC50 - -
CHEMBL2219422 AFURESERTIB IC50 - -
CHEMBL4451854 IC50 - -