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Assay Detail

CHEMBL834711

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

Functional
Inhibitory concentration against TNF-alpha production in THP-1 cells
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

THP-1 (CHEMBL614245)
Type CELL-LINE
Organism Homo sapiens

Publication

Design and synthesis of potent pyridazine inhibitors of p38 MAP kinase.
Tamayo N, Liao L, Goldberg M, Powers D, Tudor YY, Yu V, Wong LM, Henkle B, Middleton S, Syed R, Harvey T, Jang G, Hungate R, Dominguez C.
Bioorg Med Chem Lett (2005) 15 : 2409 -2413
PubMed 15837335 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 7.11 8.28

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL365359 1 8.28
CHEMBL195188 1 8.26
CHEMBL197041 1 7.81
CHEMBL265032 1 7.67
CHEMBL197267 1 7.40
CHEMBL196295 1 7.40
CHEMBL436291 1 7.30
CHEMBL193563 1 7.20
CHEMBL197096 1 7.17
CHEMBL372301 1 7.04
CHEMBL193992 1 7.03
CHEMBL426466 1 6.96
CHEMBL363600 1 6.26
CHEMBL193494 1 6.18
CHEMBL196847 1 5.91
CHEMBL193983 1 5.89

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL365359 IC50 = 5.3 nM 8.28
CHEMBL195188 IC50 = 5.5 nM 8.26
CHEMBL197041 IC50 = 15.4 nM 7.81
CHEMBL265032 IC50 = 21.5 nM 7.67
CHEMBL197267 IC50 = 40.2 nM 7.40
CHEMBL196295 IC50 = 40.2 nM 7.40
CHEMBL436291 IC50 = 50.1 nM 7.30
CHEMBL193563 IC50 = 63.6 nM 7.20
CHEMBL197096 IC50 = 67.6 nM 7.17
CHEMBL372301 IC50 = 92.2 nM 7.04
CHEMBL193992 IC50 = 93.4 nM 7.03
CHEMBL426466 IC50 = 110.0 nM 6.96
CHEMBL363600 IC50 = 552.3 nM 6.26
CHEMBL193494 IC50 = 661.0 nM 6.18
CHEMBL196847 IC50 = 1245.0 nM 5.91
CHEMBL193983 IC50 = 1286.0 nM 5.89