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Assay Detail

CHEMBL5123369

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Binding
Inhibition of CDK6/Cyclin D (unknown origin)
9
Total Activities
9
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

From Structure Modification to Drug Launch: A Systematic Review of the Ongoing Development of Cyclin-Dependent Kinase Inhibitors for Multiple Cancer Therapy.
Shi Z, Tian L, Qiang T, Li J, Xing Y, Ren X, Liu C, Liang C.
J Med Chem (2022) 65 : 6390 -6418
PubMed 35485642 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 7.76 8.70

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3904602 LEROCICLIB 3.0 1 8.70
CHEMBL3894860 TRILACICLIB 4.0 1 8.40
CHEMBL3301610 ABEMACICLIB 4.0 1 8.00
CHEMBL189963 PALBOCICLIB 4.0 1 7.80
CHEMBL4802161 DALPICICLIB 3.0 1 7.75
CHEMBL3545110 RIBOCICLIB 4.0 1 7.41
CHEMBL428690 ALVOCIDIB 3.0 1 7.22
CHEMBL445813 AT-7519 2.0 1 6.77
CHEMBL4650328 AVOTACICLIB 1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3904602 LEROCICLIB IC50 = 2.0 nM 8.70
CHEMBL3894860 TRILACICLIB IC50 = 4.0 nM 8.40
CHEMBL3301610 ABEMACICLIB IC50 = 10.0 nM 8.00
CHEMBL189963 PALBOCICLIB IC50 = 16.0 nM 7.80
CHEMBL4802161 DALPICICLIB IC50 = 18.0 nM 7.75
CHEMBL3545110 RIBOCICLIB IC50 = 39.0 nM 7.41
CHEMBL428690 ALVOCIDIB IC50 = 60.0 nM 7.22
CHEMBL445813 AT-7519 IC50 = 170.0 nM 6.77
CHEMBL4650328 AVOTACICLIB IC50 > 200.0 nM -