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Assay Detail

CHEMBL893544

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Functional
Inhibition of nitric oxide formation in human A172 cells
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A 172
Confidence 1 — Organism
Curated By Autocuration

Target

A 172 (CHEMBL614512)
Type CELL-LINE
Organism Homo sapiens

Publication

1-(1,3-Benzodioxol-5-ylmethyl)-3-[4-(1H-imidazol-1-yl)phenoxy]-piperidine analogs as potent and selective inhibitors of nitric oxide formation.
Wei RG, Adler M, Davey D, Ho E, Mohan R, Polokoff M, Tseng JL, Whitlow M, Xu W, Yuan S, Phillips G.
Bioorg Med Chem Lett (2007) 17 : 2499 -2504
PubMed 17368901 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.52 8.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL232827 1 8.05
CHEMBL233031 1 8.00
CHEMBL233032 1 7.28
CHEMBL232825 1 7.24
CHEMBL388880 1 7.11
CHEMBL233236 1 7.00
CHEMBL232255 1 6.62
CHEMBL388881 1 6.60
CHEMBL232819 1 6.19
CHEMBL396273 1 5.92
CHEMBL232818 1 5.82
CHEMBL233030 1 5.80
CHEMBL233441 1 5.80
CHEMBL232826 1 5.77
CHEMBL395498 1 5.75
CHEMBL388205 1 5.38
CHEMBL233235 1 -
CHEMBL232422 1 -
CHEMBL388417 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL232827 IC50 = 9.0 nM 8.05
CHEMBL233031 IC50 = 10.0 nM 8.00
CHEMBL233032 IC50 = 52.0 nM 7.28
CHEMBL232825 IC50 = 57.0 nM 7.24
CHEMBL388880 IC50 = 78.0 nM 7.11
CHEMBL233236 IC50 = 100.0 nM 7.00
CHEMBL232255 IC50 = 240.0 nM 6.62
CHEMBL388881 IC50 = 250.0 nM 6.60
CHEMBL232819 IC50 = 640.0 nM 6.19
CHEMBL396273 IC50 = 1200.0 nM 5.92
CHEMBL232818 IC50 = 1500.0 nM 5.82
CHEMBL233030 IC50 = 1600.0 nM 5.80
CHEMBL233441 IC50 = 1600.0 nM 5.80
CHEMBL232826 IC50 = 1700.0 nM 5.77
CHEMBL395498 IC50 = 1800.0 nM 5.75
CHEMBL388205 IC50 = 4200.0 nM 5.38
CHEMBL233235 IC50 > 10000.0 nM -
CHEMBL232422 IC50 > 10000.0 nM -
CHEMBL388417 IC50 > 10000.0 nM -