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Assay Detail

CHEMBL3878326

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

Binding
Inhibition of P-gp in human MDA435/LCC6MDR cells assessed as reduction of doxorubicin cytotoxic IC50 by half after 5 days by Cell Titer 96 Aqueous assay
2
Total Activities
2
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

Extending the structure-activity relationship study of marine natural ningalin B analogues as P-glycoprotein inhibitors.
Yang C, Wong IL, Peng K, Liu Z, Wang P, Jiang T, Jiang T, Chow LM, Wan SB.
Eur J Med Chem (2017) 125 : 795 -806
PubMed 27750197 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 2 6.77 6.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3967698 1 6.92
CHEMBL6966 VERAPAMIL 4.0 1 6.61

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3967698 EC50 = 120.0 nM 6.92
CHEMBL6966 VERAPAMIL EC50 = 245.0 nM 6.61