Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL2422646

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

Functional
Cytotoxicity against human NCI-H460 cells after 48 hrs
15
Total Activities
12
Compounds Tested
4
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type NCI-H460
Confidence 1 — Organism
Curated By Autocuration

Target

NCI-H460 (CHEMBL396)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis, and mechanism of action of 2-(3-hydroxy-5-methoxyphenyl)-6-pyrrolidinylquinolin-4-one as a potent anticancer lead.
Cheng YY, Liu CY, Tsai MT, Lin HY, Yang JS, Wu TS, Kuo SC, Huang LJ, Lee KH.
Bioorg Med Chem Lett (2013) 23 : 5223 -5227
PubMed 23916255 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.49 6.70
LC50 1 - -
TGI 1 - -
GI50 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL279142 1 6.70
CHEMBL2420526 1 6.23
CHEMBL2420525 4 5.67
CHEMBL2420524 1 4.86
CHEMBL299143 1 4.77
CHEMBL2420519 1 4.72
CHEMBL2420527 1 -
CHEMBL2420520 1 -
CHEMBL2420528 1 -
CHEMBL2420522 1 -
CHEMBL2420523 1 -
CHEMBL2420521 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL279142 IC50 = 200.0 nM 6.70
CHEMBL2420526 IC50 = 590.0 nM 6.23
CHEMBL2420525 IC50 = 2120.0 nM 5.67
CHEMBL2420524 IC50 = 13890.0 nM 4.86
CHEMBL299143 IC50 = 17000.0 nM 4.77
CHEMBL2420519 IC50 = 19130.0 nM 4.72
CHEMBL2420527 IC50 > 100000.0 nM -
CHEMBL2420520 IC50 > 100000.0 nM -
CHEMBL2420528 IC50 > 50000.0 nM -
CHEMBL2420522 IC50 > 50000.0 nM -
CHEMBL2420523 IC50 > 25000.0 nM -
CHEMBL2420521 IC50 > 25000.0 nM -
CHEMBL2420525 LC50 < 100000.0 nM -
CHEMBL2420525 TGI < 100000.0 nM -
CHEMBL2420525 GI50 = 323.59 nM -