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Assay Detail

CHEMBL4809468

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

Binding
Reversal of P-gp-mediated adriamycin resistance in human K562/A02 cells assessed as potentiation of adriamycin-induced cytotoxicity by measuring adriamycin IC50 after 48 hrs by MTT assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type K562/A02
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

ATP-dependent translocase ABCB1 (CHEMBL4302)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-Based Discovery of Pyrimidine Aminobenzene Derivatives as Potent Oral Reversal Agents against P-gp- and BCRP-Mediated Multidrug Resistance.
Qiu Q, Zou F, Li H, Shi W, Zhou D, Zhang P, Li T, Yin Z, Cai Z, Jiang Y, Huang W, Qian H.
J Med Chem (2021) 64 : 6179 -6197
PubMed 33938746 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 1 5.92 5.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4856923 1 5.92

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4856923 EC50 = 1190.0 nM 5.92