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Assay Detail

CHEMBL5165222

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

Functional
Cytotoxicity against human NCI-H1581 cells assessed as inhibition of cell growth incubated for 72 hrs by MTT assay
18
Total Activities
18
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type NCI-H1581
Confidence 1 — Organism
Curated By Autocuration

Target

NCI-H1581 (CHEMBL1075516)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and promising anti-tumor efficacy of novel imidazo[1,2-a]pyridine derivatives as potent autotaxin allosteric inhibitors.
Lei H, Wang X, Zhao G, Li T, Cui Y, Wu H, Yang J, Jiang N, Zhai X.
Eur J Med Chem (2022) 236 : 114307 -114307
PubMed 35436669 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 18 5.32 5.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5171446 1 5.39
CHEMBL5177541 1 5.32
CHEMBL5189914 1 5.32
CHEMBL5179219 1 5.25
CHEMBL5171136 1 -
CHEMBL5170680 1 -
CHEMBL5195787 1 -
CHEMBL5189398 1 -
CHEMBL3828074 ZIRITAXESTAT 3.0 1 -
CHEMBL3186509 1 -
CHEMBL5194357 1 -
CHEMBL5179154 1 -
CHEMBL5190828 1 -
CHEMBL5174427 1 -
CHEMBL5194595 1 -
CHEMBL5204526 1 -
CHEMBL5200527 1 -
CHEMBL5204000 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5171446 IC50 = 4040.0 nM 5.39
CHEMBL5177541 IC50 = 4760.0 nM 5.32
CHEMBL5189914 IC50 = 4800.0 nM 5.32
CHEMBL5179219 IC50 = 5670.0 nM 5.25
CHEMBL5171136 IC50 > 20000.0 nM -
CHEMBL5170680 IC50 > 20000.0 nM -
CHEMBL5195787 IC50 > 20000.0 nM -
CHEMBL5189398 IC50 > 20000.0 nM -
CHEMBL3828074 ZIRITAXESTAT IC50 > 20000.0 nM -
CHEMBL3186509 IC50 > 20000.0 nM -
CHEMBL5194357 IC50 - -
CHEMBL5179154 IC50 - -
CHEMBL5190828 IC50 - -
CHEMBL5174427 IC50 - -
CHEMBL5194595 IC50 - -
CHEMBL5204526 IC50 - -
CHEMBL5200527 IC50 - -
CHEMBL5204000 IC50 - -