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Assay Detail

CHEMBL4409966

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

Binding
Inhibition of kinesin (unknown origin) assessed as reduction in ATPase activity using microtubule as substrate measured for 5 to mins
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design, synthesis, and bioactivity of dihydropyrimidine derivatives as kinesin spindle protein inhibitors.
Tawfik HO, El-Moselhy TF, El-Din NS, El-Hamamsy MH.
Bioorg Med Chem (2019) 27 : 115126 -115126
PubMed 31648875 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.38 7.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1213953 1 7.00
CHEMBL4473803 1 5.41
CHEMBL4525171 1 5.40
CHEMBL4587172 1 5.36
CHEMBL4435772 1 4.97
CHEMBL4584749 1 4.85
CHEMBL236789 MONASTROL 1 4.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1213953 IC50 = 100.0 nM 7.00
CHEMBL4473803 IC50 = 3860.0 nM 5.41
CHEMBL4525171 IC50 = 3950.0 nM 5.40
CHEMBL4587172 IC50 = 4360.0 nM 5.36
CHEMBL4435772 IC50 = 10700.0 nM 4.97
CHEMBL4584749 IC50 = 14070.0 nM 4.85
CHEMBL236789 MONASTROL IC50 = 20000.0 nM 4.70