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

CHEMBL4181985

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

Functional
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 46 hrs by MTT assay
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A549
Confidence 1 — Organism
Curated By Intermediate

Target

A549 (CHEMBL392)
Type CELL-LINE
Organism Homo sapiens

Publication

Imidazo[1,2-a]pyridines linked with thiazoles/thiophene motif through keto spacer as potential cytotoxic agents and NF-κB inhibitors.
Vasu KK, Digwal CS, Pandya AN, Pandya DH, Sharma JA, Patel S, Agarwal M.
Bioorg Med Chem Lett (2017) 27 : 5463 -5466
PubMed 29138027 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 4.69 6.13

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL53463 DOXORUBICIN 4.0 1 6.13
CHEMBL4215065 1 4.83
CHEMBL4214832 1 4.73
CHEMBL4207217 1 4.65
CHEMBL4212097 1 4.64
CHEMBL4205768 1 4.25
CHEMBL4202872 1 4.25
CHEMBL4213059 1 4.07
CHEMBL4217984 1 -
CHEMBL4211161 1 -
CHEMBL4206279 1 -
CHEMBL4203396 1 -
CHEMBL4204226 1 -
CHEMBL4211571 1 -
CHEMBL4203183 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL53463 DOXORUBICIN IC50 = 740.0 nM 6.13
CHEMBL4215065 IC50 = 14710.0 nM 4.83
CHEMBL4214832 IC50 = 18580.0 nM 4.73
CHEMBL4207217 IC50 = 22460.0 nM 4.65
CHEMBL4212097 IC50 = 22760.0 nM 4.64
CHEMBL4205768 IC50 = 56910.0 nM 4.25
CHEMBL4202872 IC50 = 56880.0 nM 4.25
CHEMBL4213059 IC50 = 85250.0 nM 4.07
CHEMBL4217984 IC50 > 100000.0 nM -
CHEMBL4211161 IC50 > 100000.0 nM -
CHEMBL4206279 IC50 > 100000.0 nM -
CHEMBL4203396 IC50 > 100000.0 nM -
CHEMBL4204226 IC50 > 100000.0 nM -
CHEMBL4211571 IC50 > 100000.0 nM -
CHEMBL4203183 IC50 > 100000.0 nM -