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Assay Detail

CHEMBL853561

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

Functional
Cytotoxicity against mouse fibroblast L(tk-) cells transfected with human NMDA using LDH assay
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Mus musculus
Cell Type L929
Confidence 1 — Organism
Curated By Intermediate

Target

L cells (CHEMBL612266)
Type CELL-LINE
Organism Mus musculus

Publication

Synthesis of thieno[2,3-b]pyridinones acting as cytoprotectants and as inhibitors of [3H]glycine binding to the N-methyl-D-aspartate (NMDA) receptor.
Buchstaller HP, Siebert CD, Steinmetz R, Frank I, Berger ML, Gottschlich R, Leibrock J, Krug M, Steinhilber D, Noe CR.
J Med Chem (2006) 49 : 864 -871
PubMed 16451052 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 4.74 5.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL201440 1 5.28
CHEMBL201795 1 5.10
CHEMBL202412 1 4.81
CHEMBL263962 1 4.81
CHEMBL199848 1 4.80
CHEMBL370772 1 4.80
CHEMBL201059 1 4.25
CHEMBL383662 1 4.05
CHEMBL202705 1 -
CHEMBL382307 1 -
CHEMBL379891 1 -
CHEMBL203300 1 -
CHEMBL201235 1 -
CHEMBL203209 1 -
CHEMBL199667 1 -
CHEMBL382523 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL201440 IC50 = 5200.0 nM 5.28
CHEMBL201795 IC50 = 7900.0 nM 5.10
CHEMBL202412 IC50 = 15500.0 nM 4.81
CHEMBL263962 IC50 = 15400.0 nM 4.81
CHEMBL199848 IC50 = 15900.0 nM 4.80
CHEMBL370772 IC50 = 15700.0 nM 4.80
CHEMBL201059 IC50 = 55800.0 nM 4.25
CHEMBL383662 IC50 = 89200.0 nM 4.05
CHEMBL202705 IC50 > 50000.0 nM -
CHEMBL382307 IC50 > 50000.0 nM -
CHEMBL379891 IC50 > 200000.0 nM -
CHEMBL203300 IC50 > 250000.0 nM -
CHEMBL201235 IC50 > 30000.0 nM -
CHEMBL203209 IC50 > 50000.0 nM -
CHEMBL199667 IC50 > 50000.0 nM -
CHEMBL382523 IC50 > 250000.0 nM -