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Assay Detail

CHEMBL5129276

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

Functional
Cytotoxicity against multidrug resistance human MES-SA/Dx5 cells assessed as cell growth inhibition incubated for 144 hrs by fluorescence microplate reader assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MES-SA/Dx5
Confidence 1 — Organism
Curated By Autocuration

Target

MES-SA/Dx5 (CHEMBL613827)
Type CELL-LINE
Organism Homo sapiens

Publication

Cytotoxicity of cinchona alkaloid organocatalysts against MES-SA and MES-SA/Dx5 multidrug-resistant uterine sarcoma cell lines.
Pósa SP, Dargó G, Nagy S, Kisszékelyi P, Garádi Z, Hámori L, Szakács G, Kupai J, Tóth S.
Bioorg Med Chem (2022) 67 : 116855 -116855
PubMed 35640378 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 4.81 5.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5170136 1 5.82
CHEMBL3746148 1 5.55
CHEMBL5178595 1 5.41
CHEMBL5177677 1 4.96
CHEMBL5204885 1 4.92
CHEMBL5186527 1 4.85
CHEMBL5174200 1 4.68
CHEMBL588934 HYDROQUININE -1.0 1 4.33
CHEMBL5181372 1 4.19
CHEMBL170 QUININE 4.0 1 4.17
CHEMBL5174662 1 4.07
CHEMBL5181171 1 -
CHEMBL3747587 1 -
CHEMBL5203857 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5170136 IC50 = 1500.0 nM 5.82
CHEMBL3746148 IC50 = 2800.0 nM 5.55
CHEMBL5178595 IC50 = 3900.0 nM 5.41
CHEMBL5177677 IC50 = 11000.0 nM 4.96
CHEMBL5204885 IC50 = 12000.0 nM 4.92
CHEMBL5186527 IC50 = 14000.0 nM 4.85
CHEMBL5174200 IC50 = 21000.0 nM 4.68
CHEMBL588934 HYDROQUININE IC50 = 47000.0 nM 4.33
CHEMBL5181372 IC50 = 65000.0 nM 4.19
CHEMBL170 QUININE IC50 = 67000.0 nM 4.17
CHEMBL5174662 IC50 = 85000.0 nM 4.07
CHEMBL5181171 IC50 = 105000.0 nM -
CHEMBL3747587 IC50 = 197000.0 nM -
CHEMBL5203857 IC50 = 161000.0 nM -