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Assay Detail

CHEMBL4769112

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

ADMET
Cytotoxicity against human K562 cells assessed as reduction in cell viability incubated for 72 hrs by MTS assay
8
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type ADMET
Organism Homo sapiens
Cell Type K562
Confidence 1 — Organism
Curated By Autocuration

Target

K562 (CHEMBL385)
Type CELL-LINE
Organism Homo sapiens

Publication

Substituted oxindol-3-ylidenes as AMP-activated protein kinase (AMPK) inhibitors.
Matheson CJ,Casalvieri KA,Backos DS,Minhajuddin M,Jordan CT,Reigan P
Eur J Med Chem (2020) 197 : 112316 -112316
PubMed 32334266 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 8 5.09 5.54

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4779166 1 5.54
CHEMBL4796639 1 5.42
CHEMBL4799798 1 5.17
CHEMBL535 SUNITINIB 4.0 1 5.14
CHEMBL13976 1 4.90
CHEMBL3542344 1 4.87
CHEMBL4788980 1 4.87
CHEMBL4788376 1 4.83

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4779166 EC50 = 2850.0 nM 5.54
CHEMBL4796639 EC50 = 3830.0 nM 5.42
CHEMBL4799798 EC50 = 6790.0 nM 5.17
CHEMBL535 SUNITINIB EC50 = 7230.0 nM 5.14
CHEMBL13976 EC50 = 12550.0 nM 4.90
CHEMBL3542344 EC50 = 13590.0 nM 4.87
CHEMBL4788980 EC50 = 13480.0 nM 4.87
CHEMBL4788376 EC50 = 14780.0 nM 4.83