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Assay Detail

CHEMBL2328973

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

Binding
Inhibition of human Cdc7 using biotin-C6linker-TPSDSLIYDDGLS as substrate after 1 hr
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

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

Publication

Azaindole-Based Inhibitors of Cdc7 Kinase: Impact of the Pre-DFG Residue, Val 195.
Tong Y, Stewart KD, Florjancic AS, Harlan JE, Merta PJ, Przytulinska M, Soni N, Swinger KK, Zhu H, Johnson EF, Shoemaker AR, Penning TD.
ACS Med Chem Lett (2013) 4 : 211 -215
PubMed 24900653 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 13 8.31 9.55

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1958408 1 9.55
CHEMBL2322677 1 9.05
CHEMBL2322674 1 8.85
CHEMBL2322683 1 8.77
CHEMBL2322682 1 8.49
CHEMBL2322684 1 8.47
CHEMBL2322675 1 8.26
CHEMBL2322673 1 8.11
CHEMBL2322678 1 8.06
CHEMBL2322679 1 7.89
CHEMBL2322680 1 7.82
CHEMBL2322681 1 7.57
CHEMBL2322676 1 7.17

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1958408 Ki = 0.28 nM 9.55
CHEMBL2322677 Ki = 0.9 nM 9.05
CHEMBL2322674 Ki = 1.4 nM 8.85
CHEMBL2322683 Ki = 1.7 nM 8.77
CHEMBL2322682 Ki = 3.2 nM 8.49
CHEMBL2322684 Ki = 3.4 nM 8.47
CHEMBL2322675 Ki = 5.5 nM 8.26
CHEMBL2322673 Ki = 7.7 nM 8.11
CHEMBL2322678 Ki = 8.7 nM 8.06
CHEMBL2322679 Ki = 13.0 nM 7.89
CHEMBL2322680 Ki = 15.0 nM 7.82
CHEMBL2322681 Ki = 27.0 nM 7.57
CHEMBL2322676 Ki = 67.0 nM 7.17