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

CHEMBL3777659

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

Binding
Inhibition of CDK7 (unknown origin)
3
Total Activities
3
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

Cyclin-dependent kinase 7 (CHEMBL3055)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

5-Substituted 3-isopropyl-7-[4-(2-pyridyl)benzyl]amino-1(2)H-pyrazolo[4,3-d]pyrimidines with anti-proliferative activity as potent and selective inhibitors of cyclin-dependent kinases.
Vymětalová L, Havlíček L, Šturc A, Skrášková Z, Jorda R, Pospíšil T, Strnad M, Kryštof V.
Eur J Med Chem (2016) 110 : 291 -301
PubMed 26851505 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.22 6.87

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1801932 1 6.87
CHEMBL3774632 1 5.56
CHEMBL189963 PALBOCICLIB 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1801932 IC50 = 134.0 nM 6.87
CHEMBL3774632 IC50 = 2780.0 nM 5.56
CHEMBL189963 PALBOCICLIB IC50 > 10000.0 nM -