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Assay Detail

CHEMBL998766

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Binding
Inhibition of CDC7-DBF4
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Cell division cycle 7-related protein kinase (CHEMBL5443)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

4-(1H-indazol-5-yl)-6-phenylpyrimidin-2(1H)-one analogs as potent CDC7 inhibitors.
Shafer CM, Lindvall M, Bellamacina C, Gesner TG, Yabannavar A, Jia W, Lin S, Walter A.
Bioorg Med Chem Lett (2008) 18 : 4482 -4485
PubMed 18672368 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.26 8.52

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL501724 1 8.52
CHEMBL508883 1 8.30
CHEMBL500662 1 8.22
CHEMBL502268 1 8.00
CHEMBL526133 1 8.00
CHEMBL450151 1 7.52
CHEMBL501732 1 7.40
CHEMBL501731 1 7.00
CHEMBL502538 1 6.96
CHEMBL502269 1 6.82
CHEMBL501462 1 6.46
CHEMBL524866 1 6.00
CHEMBL501723 1 5.14
CHEMBL524899 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL501724 IC50 = 3.0 nM 8.52
CHEMBL508883 IC50 = 5.0 nM 8.30
CHEMBL500662 IC50 = 6.0 nM 8.22
CHEMBL502268 IC50 = 10.0 nM 8.00
CHEMBL526133 IC50 = 10.0 nM 8.00
CHEMBL450151 IC50 = 30.0 nM 7.52
CHEMBL501732 IC50 = 40.0 nM 7.40
CHEMBL501731 IC50 = 100.0 nM 7.00
CHEMBL502538 IC50 = 110.0 nM 6.96
CHEMBL502269 IC50 = 150.0 nM 6.82
CHEMBL501462 IC50 = 350.0 nM 6.46
CHEMBL524866 IC50 = 1000.0 nM 6.00
CHEMBL501723 IC50 = 7300.0 nM 5.14
CHEMBL524899 IC50 > 13000.0 nM -