Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL944055

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

Functional
Antiproliferative activity against human A2780 cells after 72 hrs
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A2780
Confidence 1 — Organism
Curated By Autocuration

Target

A2780 (CHEMBL614004)
Type CELL-LINE
Organism Homo sapiens

Publication

Cdc7 kinase inhibitors: pyrrolopyridinones as potential antitumor agents. 1. Synthesis and structure-activity relationships.
Vanotti E, Amici R, Bargiotti A, Berthelsen J, Bosotti R, Ciavolella A, Cirla A, Cristiani C, D'Alessio R, Forte B, Isacchi A, Martina K, Menichincheri M, Molinari A, Montagnoli A, Orsini P, Pillan A, Roletto F, Scolaro A, Tibolla M, Valsasina B, Varasi M, Volpi D, Santocanale C.
J Med Chem (2008) 51 : 487 -501
PubMed 18201066 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 6.02 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL399492 1 7.00
CHEMBL253545 1 6.70
CHEMBL253768 1 6.10
CHEMBL225519 1 5.96
CHEMBL402272 1 5.77
CHEMBL250693 1 5.33
CHEMBL1203954 1 5.26
CHEMBL254597 1 -
CHEMBL253760 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL399492 IC50 = 100.0 nM 7.00
CHEMBL253545 IC50 = 200.0 nM 6.70
CHEMBL253768 IC50 = 800.0 nM 6.10
CHEMBL225519 IC50 = 1100.0 nM 5.96
CHEMBL402272 IC50 = 1700.0 nM 5.77
CHEMBL250693 IC50 = 4700.0 nM 5.33
CHEMBL1203954 IC50 = 5500.0 nM 5.26
CHEMBL254597 IC50 > 10000.0 nM -
CHEMBL253760 IC50 > 10000.0 nM -