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Assay Detail

CHEMBL653816

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Binding
Inhibitory activity against Calcium/calmodulin-dependent protein kinase type II using autocamtide as substrate
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

CaM kinase II (CHEMBL2097164)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Synthesis, structure-activity relationship, and biological studies of indolocarbazoles as potent cyclin D1-CDK4 inhibitors.
Zhu G, Conner SE, Zhou X, Shih C, Li T, Anderson BD, Brooks HB, Campbell RM, Considine E, Dempsey JA, Faul MM, Ogg C, Patel B, Schultz RM, Spencer CD, Teicher B, Watkins SA.
J Med Chem (2003) 46 : 2027 -2030
PubMed 12747775 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.33 7.24

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL59785 1 7.24
CHEMBL292021 1 7.09
CHEMBL293157 1 7.04
CHEMBL293898 1 6.76
CHEMBL64742 1 6.63
CHEMBL291402 1 6.04
CHEMBL432715 1 4.96
CHEMBL64758 1 4.91
CHEMBL302854 1 -
CHEMBL60564 1 -
CHEMBL62253 1 -
CHEMBL268368 STAUROSPORINE AGLYCON 1 -
CHEMBL61790 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL59785 IC50 = 58.0 nM 7.24
CHEMBL292021 IC50 = 82.0 nM 7.09
CHEMBL293157 IC50 = 92.0 nM 7.04
CHEMBL293898 IC50 = 174.0 nM 6.76
CHEMBL64742 IC50 = 236.0 nM 6.63
CHEMBL291402 IC50 = 914.0 nM 6.04
CHEMBL432715 IC50 = 11100.0 nM 4.96
CHEMBL64758 IC50 = 12400.0 nM 4.91
CHEMBL302854 IC50 > 2000.0 nM -
CHEMBL60564 IC50 < 1250.0 nM -
CHEMBL62253 IC50 > 2000.0 nM -
CHEMBL268368 STAUROSPORINE AGLYCON IC50 < 125.0 nM -
CHEMBL61790 IC50 > 2000.0 nM -