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Assay Detail

CHEMBL3111101

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

Binding
Inhibition of CDK2/cyclin A3 (unknown origin)
3
Total Activities
3
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

8-Substituted O(6)-cyclohexylmethylguanine CDK2 inhibitors: using structure-based inhibitor design to optimize an alternative binding mode.
Carbain B, Paterson DJ, Anscombe E, Campbell AJ, Cano C, Echalier A, Endicott JA, Golding BT, Haggerty K, Hardcastle IR, Jewsbury PJ, Newell DR, Noble ME, Roche C, Wang LZ, Griffin RJ.
J Med Chem (2014) 57 : 56 -70
PubMed 24304238 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 6.37 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL319467 1 8.30
CHEMBL122264 1 6.01
CHEMBL269881 1 4.80

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL319467 IC50 = 5.0 nM 8.30
CHEMBL122264 IC50 = 970.0 nM 6.01
CHEMBL269881 IC50 = 16000.0 nM 4.80