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Assay Detail

CHEMBL3419829

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Binding
Inhibition of Mnk2 (unknown origin) pre-incubated for 10 mins before eIF4E peptide substrate addition by ADP-Glo kinase assay
14
Total Activities
14
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

Publication

Discovery of 4-(dihydropyridinon-3-yl)amino-5-methylthieno[2,3-d]pyrimidine derivatives as potent Mnk inhibitors: synthesis, structure-activity relationship analysis and biological evaluation.
Yu M, Li P, Basnet SK, Kumarasiri M, Diab S, Teo T, Albrecht H, Wang S.
Eur J Med Chem (2015) 95 : 116 -126
PubMed 25800647 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 14 5.88 6.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3417199 1 6.62
CHEMBL3417205 1 6.47
CHEMBL3417198 1 6.46
CHEMBL1240885 1 6.06
CHEMBL3417207 1 6.05
CHEMBL3417208 1 5.80
CHEMBL3417204 1 5.58
CHEMBL3417203 1 5.50
CHEMBL3417202 1 5.22
CHEMBL3417201 1 5.04
CHEMBL3417206 1 -
CHEMBL3417200 1 -
CHEMBL3417197 1 -
CHEMBL3417196 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3417199 Ki = 240.0 nM 6.62
CHEMBL3417205 Ki = 340.0 nM 6.47
CHEMBL3417198 Ki = 350.0 nM 6.46
CHEMBL1240885 Ki = 880.0 nM 6.06
CHEMBL3417207 Ki = 900.0 nM 6.05
CHEMBL3417208 Ki = 1600.0 nM 5.80
CHEMBL3417204 Ki = 2630.0 nM 5.58
CHEMBL3417203 Ki = 3170.0 nM 5.50
CHEMBL3417202 Ki = 5990.0 nM 5.22
CHEMBL3417201 Ki = 9050.0 nM 5.04
CHEMBL3417206 Ki > 10000.0 nM -
CHEMBL3417200 Ki > 10000.0 nM -
CHEMBL3417197 Ki > 10000.0 nM -
CHEMBL3417196 Ki > 10000.0 nM -