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Assay Detail

CHEMBL888214

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

Binding
Inhibition of NF-kappaB-mediated gene transcription in HepG2 cells by luciferase reporter gene assay
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HepG2
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Structure-activity studies of phenanthroindolizidine alkaloids as potential antitumor agents.
Gao W, Bussom S, Grill SP, Gullen EA, Hu YC, Huang X, Zhong S, Kaczmarek C, Gutierrez J, Francis S, Baker DC, Yu S, Cheng YC.
Bioorg Med Chem Lett (2007) 17 : 4338 -4342
PubMed 17531481 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 7.07 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL250854 TYLOPHORINIDINE 1 8.00
CHEMBL250474 1 7.96
CHEMBL398325 TYLOPHORININE 1 7.92
CHEMBL399965 1 6.50
CHEMBL400888 1 6.49
CHEMBL401479 TYLOPHORIDICINE F 1 6.43
CHEMBL249029 TYLOPHORIDICINE C 1 6.22
CHEMBL399317 1 -
CHEMBL53004 TYLOPHORIDICINE E 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL250854 TYLOPHORINIDINE IC50 = 10.0 nM 8.00
CHEMBL250474 IC50 = 11.0 nM 7.96
CHEMBL398325 TYLOPHORININE IC50 = 12.0 nM 7.92
CHEMBL399965 IC50 = 315.0 nM 6.50
CHEMBL400888 IC50 = 322.0 nM 6.49
CHEMBL401479 TYLOPHORIDICINE F IC50 = 367.0 nM 6.43
CHEMBL249029 TYLOPHORIDICINE C IC50 = 600.0 nM 6.22
CHEMBL399317 IC50 > 300.0 nM -
CHEMBL53004 TYLOPHORIDICINE E IC50 > 1000.0 nM -